УСТРОЙСТВО ДЛЯ НАЛОЖЕНИЯ ПОДВЕСНОЙ ХОЛЕЦИСТОСТОМЫ

Устройство относится к медицине и может быть использовано в эндобилиарной хирургии. Конструкция состоит из рабочей части, вводимой в полость, манипулятора, позволяющего управлять рабочей частью, и катетера с тройником. Рабочая часть конструкции включает центральный силовой стержень и четыре симметрично расположенные бранши. Бранши выполняются из проволоки биологически инертного материала-никелида титана, обладающего эффектом сверупругости. Бранши и силовой стержень соединены с манипулятором, позволяющим посредством перемещения имеющихся на нем клавиш управлять браншами и силовым стержнем в отдельности и одновременно. В результате получается оптимальная конструкция дилататора-фиксатора из биологически инертного материала, позволяющего кардинально упростить процедуру наложения подвесной холецистостомы с целью последующей эвакуации желчи и введения медикаментов. 4 з.п.ф-лы, 3 ил.

ЛАПАРОСКОПИЧЕСКОЕ УСТРОЙСТВО ДЛЯ РАСШИРЕНИЯ ЖЕЛЧНЫХ ПРОТОКОВ

Полезная модель относится к медицинским устройствам для проведения хирургических лапароскопических операций, а именно для расширения желчных протоков. Устройство состоит из корпуса, толкателя и рукоятки, к корпусу прикреплены с помощью осей четыре губки, раскрываемые или смыкаемые между собой с помощью головки толкателя, причем к толкателю прикреплен штифт, передающий движение от рукоятки, присоединенной к корпусу с помощью оси, при этом толкатель может быть зафиксирован стопорным винтом. Применение данного устройства в клинической практике позволяет четко визуализировать все стенки желчного протока при лапароскопических операциях и произвести прошивание протока без угрозы критического сужения за счет вовлечения в шовный материал соседних стенок протока. Предложенное устройство промышленно применимо, просто в изготовлении и использовании, не требует больших затрат. 2 ил.

КАТЕТЕРНЫЙ НАСОС, КОТОРЫЙ СОДЕРЖИТ БЛОК ПРИВОДА, И КАТЕТЕР

Изобретение относится к области медицинской техники, а именно к катетерному насосу, используемому в качестве системы временной циркуляторной поддержки в артериальном сосудистом русле, например в аорте пациентов, в частности, когда природное сердце неспособно обеспечивать организм достаточно оксигенированной кровью. Катетерный насос, имеющий катетер, имеющий головку насоса, предусмотренную на дистальном конце катетера для введения в артериальную сосудистую систему, содержит внешний катетер и внутренний катетер, расположенный во внешнем катетере, который имеет вал ротора, расположенный с возможностью поворота во внутреннем катетере для приведения в действие расширяемого переносящего элемента, предусмотренного на головке насоса, имеющей исполнительную часть, предусмотренную на проксимальном конце катетера, посредством которой вал ротора можно приводить в действие, и имеет клетку, окружающую переносящий элемент. Клетка имеет дистальную и проксимальную муфты и филаменты, проходящие между муфтами ...

ЭЛЮТИРУЮЩИЕ МЕДИЦИНСКИЕ УСТРОЙСТВА

... 1. Медицинское устройство, содержащее:a. расширяемый элемент;b. покрытие, содержащее лекарственное средство, расположенное вокруг указанного расширяемого элемента;c. оболочку с внешней поверхностью и внутренней поверхностью, имеющую микроструктуру изменяемой проницаемости, которая сначала ограничивает непреднамеренное прохождение указанного лекарственного средства сквозь указанную оболочку, когда микроструктура указанной оболочки является закрытой;d. в котором указанное покрытие расположено на внутренней поверхности указанной оболочки; иe. в котором, когда указанный расширяемый элемент и оболочка находятся в расширенном состоянии, микроструктура указанной оболочки является открытой и позволяет лекарственному средству выходить наружу сквозь указанную оболочку.2. Медицинское устройство по п. 1, отличающееся тем, что указанное покрытие и лекарственное средство выходят в пространство, находящееся снаружи от указанной оболочки.3. Медицинское устройство по п. 1, отличающееся тем, что указанная ...

Устройство для остановки кровотечения в пищеводе

Изобретение относится к медицинской технике, в частности к устройствам для остановки кровотечений в пищеводе. Цель изобретения - уменьшение травматизации при проведении по пищеводу и предупреждение пролежней и возникновения пневмонии. Устройство содержит гибкую втулку 2 с баллонами 3 и 4 и манжетой 5 с пазами. В стенке втулки 2 выполнены каналы, один из которых сквозной через пазы и каналы втулки 2 проходят воздуховоды 6 и 7 баллонов 3 и 4. 4 ил.

Trokarhülse

The invention concerns a trocar sheath for endoscopic use, the trocar sheath comprising an elongate part having at least one channel into which an instrument, for example, an endoscope, scissors, or the like, can be inserted, and, at the distal end, movable, pivotable parts. The trocar sheath according to the invention is characterized in that its distal region is formed by a plurality of longitudinal sections which are articulated on the proximal part of the trocar sheath, A mechanism is provided which pivots the individual longitudinal sections about an axis perpendicular to the longitudinal axis of the trocar sheath.

Urethro-renoscope for removal of kidney stones, comprises rigid hollow shaft accommodating catheter with elastic tip

A rigid shaft (1) accommodates the catheter (2) of an endoscope comprising a connection (29,30) for an optical and lighting unit, an operating duct, and a rinsing duct (9). The catheter (2) has a flexible front (3) to be adjusted in shape by a control device (4) and to be axially moved inside the shaft (1). The sliding element (5) is attached to a stationary part (6) also holding the shaft (1) guided through a bore (8) in its center. Marks at the sliding element (5) indicate the length of the catheter segment (3) located outside the shaft (1).

CHOLANGIOGRAPHIEKATHETER

Taktiler Messkopf

Taktiler Messkopf (10) zum Einführen in den Körper eines Patienten während eines minimalinvasiven chirurgischen Eingriffs, wobei der taktile Messkopf (10) eine expandierbare und wieder komprimierbare Trägervorrichtung (12), eine Sensorvorrichtung (14), die mit der Trägervorrichtung (12) mechanisch verbunden ist und von dieser getragen wird, wenn sich diese in ihrem expandierten Zustand befindet, aufweist.

SYSTEM ZUM EINFÜHREN EINER GEFÄSSPROTHESE

KLAPPENPROTHESE ZUM VERHINDERN EINER ABFLUSSOBSTRUKTION

Eine Mitralklappenprothese kann in eine natürliche Mitralklappe verankert werden. Die Mitralklappenprothese weist bevorzugt ein großes anteriores Prothesensegel auf, welches die gesamte Breite des natürlichen anterioren Segels überspannt, wobei das anteriore Prothesensegel während der Systole weg von dem linken ventrikulären Ausflusstrakt verläuft, um einen unversperrten Ausflusspfad zu erzeugen.

Transcutaner Implantatkatheter.

KATHETER

Surgical implement

Lock mechanism for a catheter

The invention comprises a catheter having an inner 20 and outer 10 sleeves which are displaceable relative to each other and a lock mechanism 50 having a releaser 70 in the form frangible tab which when unlocking the sleeves breaks along lines of weakness 66, 68. The lock may comprise first and second lock components 54, 56 positioned on the sleeves which engage to hold the relative positions of the sleeves. The lock may comprise an adapter mounted on the outer sleeve (figs 7-11).

Urinary drainage catheter

Pulmonary nodule access devices and methods of using the same

In certain embodiments, a device is configured to be delivered to the site of a nodule in the lung or other body organ or lumen. The device can be configured to attach directly to the target nodule or to tissue adjacent the target nodule. The device can be configured t provide repeatable access to the site of the target nodule. In some embodiments, the device includes a guide wire that can extend proximal the device. In some embodiments, the device can include a channel portion through which medical devices and/or instruments can be navigated. In some embodiments, the device can be deployed in the wall of an airway or other body lumen to provide trans luminal access to a nodule outside of the lumen.

Catheter

A catheter comprising a tip member 10 at its distal end 120, an elongated tube 20, and a retention mechanism 30 comprising a plurality of wings 31, the wings being provided with shape memory alloy wires 40 configured to cause the wings to transition from a deactivated shape (41, Fig 4a), for passing through a bodily channel during insertion and/or removal of the catheter from a bodily cavity, to an activated shape 42, for retention of the catheter inside the bodily cavity. Each wing has a distal extremity 33 connected to the tip member at least during insertion of the catheter, and a proximal extremity 32 connected to the elongated tube at least when the wings are in the activated shape. In one arrangement, after the wings are transitioned to the activated shape, the tip is detached from the wings and removed (Fig 6-7). The tube may me moveable from a first position in which it covers and constrains the wings to a second position in which it exposes the wings and abuts the proximal extremities ...

Spring guide manipulator

... 1,119,159. Manipulative tool for spring guides. UNITED STATES CATHETER & INSTRUMENT CORP. 17 Feb., 1967 [31 May, 1966], No. 7689/67. Heading A5R. [Also in Division F2] A manipulative tool for spring guides comprises a body portion A, a front chuck B for securely holding the proximal end coils of a spring guide, the front chuck being operably connected to the body portion and rotatable with respect thereto about its longitudinal axis, a back chuck C for securely holding the proximal end of a spring guide tensioning wire, the back chuck being operably associated with the front chuck and being rotatable therewith and axially movable with respect thereto, wheel D for rotating both chucks relative to the body portion, and a linkage assembly E for effecting axial movement of the back chuck C towards or away from the front chuck B. Body portion A includes flange 5 connected to mounting block 6 by spacer rod 7. Block 6 has a vertical rib 8, a pair of horizontal slideways 9, 9, and relatively large ...

PROSTHETIC SPHINCTER DEVICE

SIGMOIDOSCOPIC DEFLATION DEVICE

ORGAN ACCESS SYSTEMS AND TROCAR ASSEMBLIES

CATHETER PROVIDED WITH A SAFETY-FIXING MEMBER REMOTELY ADJUSTABLE AND EXPANDIBLE BY INTRODUCING FLUIDS

CATHETERS

... 1536019 Retention catheter with seal E L ADAIR 24 Feb 1976 07137/76 Heading ASR A catheter comprises distally connected inner and outer, relatively slidable, flexible tubes 14, 12, the outer one 14 of which is provided with axial or helical slits 18 whereby strips 20 buckle outwardly upon relative outward axial movement of the inner tube. Movement of the inner tube causes a seal 40 and retaining arrangement 42 to engage against a conical wall 28 and lock the tubes relative to each other and prevent fluid leakage from between them. The tubes 12, 14 are joined at their inner end, e.g. by heat sealing 16, cement, or a reverse fold Fig. 4 (not shown) of the outer tube. A rigid sharp ended trocar 46 may be provided for movement by plunger 48. In an alternative form of the seal and retaining arrangement a flexible ratchet type assembly can be used Fig. 2 (not shown). Alternatively a resilient bellows connection between the outer tube and housing 36 is prevented from expanding by a removable clip ...

ADAPTABLE BALLOON-LOOSE OF KATHEDER

GUIDANCE WIRE AS EMBOLIESCHUTZ WITH ACTIVATE-CASH ATTACK AND FILTER

SMOOTH HOLDING DEVICE

DEVICE FOR REMOVING FROM OKKLUSIONEN IN BIOLOGICAL PASSAGES

SEAM CASE WITH LINE LOCKING DEVICE

MECHANISM FOR THE ESTABLISHMENT OF A PROBE HEAD, IN PARTICULAR FOR KARDIALSONDEN

DEVICE TO INTERKOSTALEN AND LUMBAREN PERFUSION

DRAINAGE CATHETER

DEVICE TO KANÜLIERUNG A BLOOD-PROMINENT CONTAINER

BI-DIRECTIONAL FEMORALARTERIENKANÜLE.

CATHETER FOR THE PERCUTANEOUS GASTROSTOMIE.

DEVICE FOR THE ANALYSIS OF THE DEGREE OF THE FABRIC DAMAGE IN A HEART THE INSUFFICIENT ARTERIAL ONE BLUTSTRÖMUNG SUSPENDED.

INTERMITTENT CATCH OF THE CORONAR SINE WITH PRINTING PRESSURE.

SET FOR THE CREATION OF AN ARTIFICIAL CARDIA

DISCHARGE DEVICE FOR MEDICINES INTO THE HEART BAG FOR ANGIOGENESIS

KANÜLE TO THE SELECTIVE ONE, PRESSURE-DEPENDENT ADMINISTRATION OF THERAPEUTIC SUBSTANCES

INJEKTIONSGERÄT

MEDICAL INSTRUMENT

DEVICE FOR LEADING A GUIDANCE WIRE AND FOR CONNECTING WITH A GUIDANCE WIRE EXTENSION

INTO A BODY CHANNEL BRING IN-CASH INSTRUMENT WITH BI-DIRECTIONAL COEFFICIENT OF THE OBERFLÄCHENREIBUNG WITH BODY FABRIC

FLEXIBLE RETAINING FLANGE FOR NOURISHING PROBE

VASKULARE DILATATIONSVORRICHTUNG

Anchor system for retaining a device in tissue

A lead device is provided for a medical treatment apparatus, where the lead device includes mechanisms for anchoring the lead device in tissue.

Introducing stylet

An introducing stylet is configured for insertion into an endotracheal tube (ETT) and includes an elongated rod having a distal end and a proximal end, and a positioning feature formed on the rod and configured to engage the ETT to prevent both longitudinal and lateral movement of the introducing stylet relative to the ETT. A portion of the distal end of the rod that extends longitudinally outwardly of the ETT and defines a leading end.

Valve assembly and retainer for surgical access assembly

VALVE ASSEMBLY AND RETAINER FOR SURGICAL ACCESS A surgical access assembly (100) comprising: a cannula (102); a valve housing (110) coupled to a proximal end of the cannula (102); and a valve assembly (120) disposed in the valve housing (110), the valve assembly (120) including: a centering mechanism (130) including a hoop (132) having fingers extending radially outwards from an outer surface of the hoop (132), each finger being flexibly connected to the outer surface and biased away from the outer surface; a ring (122) with an outer diameter and a flange (124) disposed at one end of the ring (122), the other end of the ring (122) abutting one end of the hoop (132); a retainer (200) having a first disc disposed in the ring (122) and a second disc disposed in the hoop (132), the first disc attachable to the second disc irrespective of the rotational orientation of the first disc relative to the second disc; a guard (140) including a frame (148) and flaps flexibly coupled thereto, the guard ...

URETERAL AND BLADDER CATHETERS AND METHODS FOR INDUCING NEGATIVE PRESSURE TO INCREASE RENAL PERFUSION

Ureteral catheters and assemblies are provided including: a drainage lumen including a proximal portion configured to be positioned in at least a portion of a patient's urethra and a distal portion configured to be positioned in a patient's ureter and/or kidney, the distal portion including a coiled retention portion including at least a first coil having a first diameter and a second coil having a second diameter, the first diameter being less than the second diameter; or wherein the retention portion extends radially outwardly from a portion of the distal end of the drainage lumen portion, the retention portion including a proximal end having a first diameter, a distal end having a second diameter, and a wall and/or surface extending therebetween, the retention portion having a second diameter is greater than the first diameter when deployed; or wherein the retention portion includes a plurality of drainage tubes. 13 132 21 130 121212 1181F 118 1210 124 140t ...

Anchoring system for a catheter or the like

Seizing instrument

Prostatic stent with localized tissue engaging anchoring means

Uretral stent and related methods

Indwelling urinary catheter with enlarged sealing surface

Probe for the enteral nutrition of a patient

The invention relates to a probe (1) for the enteral nutrition of a patient, comprising a tube section (16), which is extended along an axial direction (S) at least in some sections and which has a proximal end (161) and a distal end (160), and comprising a retaining device (12, 13), which is arranged at the distal end (160) of the tube section (16). In a compressed state, the retaining device projects past the distal end (160) of the tube section at least in one direction that is radial with respect to the axial direction (S), and in an extended state, in which the retaining device (12, 13) is extended along the axial direction (S), the retaining device has a smaller radial expansion in comparison to the compressed state. The retaining device (12, 13), in cooperation with an actuating device (2), can be transferred from the compressed state into the extended state. For this purpose, the tube section is made of an outer tube (16), and an inner tube (15) that has a proximal end (151) and ...

Internal reference coronary sinus catheter

Gastrostomy device package and method of assembly

CATHETER KIT FOR GASTRIC ULCER

Programmable flexible-tube flow regulator and use methods

Tube having a retention member

Conformable balloonless catheter

Device and method for intra-bronchial provision of a therapeutic agent

CONDUITS FOR MAINTAINING OPENINGS IN TISSUE

Covering for a medical scoping device

The present invention relates to a cover having a plurality of moveable, external, angled 5 projecting elements for use with flexible medical scoping devices such as endoscopes or enteroscopes. The invention includes the cover with an over cuff and use of the disposable removable covering in methods of medical scoping procedures or examinations. The invention also includes an applicator for assisting in placing the covering about or over a medical device and a kit of parts.

Expandable body device and method of use

Disclosed herein are medical devices comprising a single-lobed, thin-walled, expandable body and a flexible, elongated delivery device for treating saccular vascular aneurysms and occluding segments of blood vessels and other biological conduits. The expandable bodies may include gold and other metals that can be compressed, positioned in the lumen of an aneurysm, or other biological conduit and expanded. The external surface of the expandable bodies can be configured to promote local thrombosis and to promote the growth of tissue into and around the surface in order to reduce migration of the expandable body and to occlude and seal the aneurysm or biological conduit. For the treatment of saccular aneurysms, the expandable body may be deployed in combination with one or more coiled wires that contact both the wall of the aneurysm and the expandable body and exert force on the expandable body to aid in sealing the aneurysm neck.

Ureteral and bladder catheters and methods for inducing negative pressure to increase renal perfusion

Ureteral catheters and assemblies provided including: a drainage lumen including a proximal portion configured to be positioned in at least a portion of a patient's urethra and a distal portion configured to be positioned in a patient's ureter and/or kidney, the distal portion including a coiled retention portion including at least a first coil having a first diameter and a second coil having a second diameter, the first diameter being less than the second diameter; or wherein the retention portion extends radially outwardly from a portion of the distal end of the drainage lumen portion, the retention portion including a proximal end having a first diameter, a distal end having a second diameter, and a wall and/or surface extending there between, the retention portion having a second diameter is greater than the first diameter when deployed; or wherein the retention portion includes a plurality of drainage tubes.

Apparatus and methods of bioelectrical impedance analysis of blood flow

Apparatus and methods of bioelectrical impedance analysis of blood flow

CATHETER

Method for pressure mediated selective delivery of therapeutic substances and cannula

PLACING A GUIDE MEMBER INTO THE HEART

A guide member (120) positioned through a coronary vessel, and the wall of the heart provides access to a heart chamber. A first end of the guide member (120) is passed through the coronary vessel, the heart wall into the heart chamber, and then is passed back out of the heart chamber. The end of the guide member (120) may then be used to deliver devices into the heart chamber to carry out various medical procedures. A conduit delivery system (110) is coupled to the end of the guide member, is delivered into the heart chamber, and then used to place a conduit in the heart wall to communicate the coronary vessel with the heart chamber.

PERITONEAL DIALYSIS CATHETER

METHOD FOR PRESSURE MEDIATED SELECTIVE DELIVERY OF THERAPEUTIC SUBSTANCES AND CANNULA

Methods and devices are disclosed for selective delivery of therapeutic substances to specific histologic or microanatomic areas of organs. Introduction of the therapeutic substance into a hollow organ space (such as an hepatobiliary duct or the gallbladder lumen) at a controlled pressure, volume or rate allows the substance to reach a predetermined cellular layer (such as the epithelium or sub-epithelial space). The volume or flow rate of the substance can be controlled so that the intralumenal pressure reaches a predetermined threshold level beyond which subsequent subepithelial delivery of the substance occurs. Alternatively, a lower pressure is selected that does not exceed the threshold level, so that delivery occurs substantially only to the epithelial layer. Such site specific delivery of therapeutic agents permits localized delivery of substances (for example to the interstitial tissue of an organ) in concentrations that may otherwise produce systemic toxicity. Occlusion of venous ...

PARTIAL AORTIC OCCLUSION DEVICES AND METHODS FOR CEREBRAL PERFUSION AUGMENTATION

Methods are provided for partial aortic obstruction for cerebral perfusion augmentation in patients suffering from global or focal cerebral ischemia. Alternatively, the methods can be used to partially obstruct aortic blood flow to condition the spinal cord to secrete neuroprotective agents prior to abdominal aortic aneurysm repair. Partial obstruction of a vessel can be accomplished by a device comprising an elongate catheter (102) and a distally mounted expandable member (104).The expandable member (104) may comprise one or two balloons. Other medical devices, such as an angioplasty, stent, or atherectomy catheter, can be inserted distal the expandable member to provide therapeutic intervention.

IMPROVED COLOSTOMY DEVICE

An improved colostomy device is provided for preventing the external and internal balloons from being pushed into the upper part of the rectum as well as preventing the leakage of liquids and gases with its perfect air-tight feature and for helping insert the colostomy device to the patients. When composing a colostomy device with internal and external balloons and a drainage hose, a fixing aid is disposed on the external side of the drainage hose and the front end sides of the rim of the supporting tube is wrapped by a protection membrane between the internal and external balloons.

GASTRIC BALLOON CATHETER WITH IMPROVED BALLOON ORIENTATION

A balloon catheter with improved balloon orientation includes a head, a catheter segment extending from the head, and a balloon disposed on the catheter segment opposite the head. Preferably, the balloon is attached to the exterior of the catheter segment at a proximal location and to the interior of the catheter segment at a distal location to thereby form a balloon which extends distally from the distal end of the catheter segment when inflated. The improved orientation of the balloon helps to prevent contact between the distal end of the catheter segment and anatomical structures of the user, thereby reducing irritation.

DEVICES AND SYSTEMS FOR ESTABLISHING SUPPLEMENTAL CIRCULATORY BLOOD FLOW

A blood circulation assist system comprising an inflow cannula (12) having a lumen and an insertion device (200) configured to be received therein and to facilitate insertion of a portion of the inflow cannula (12) into a heart chamber. The insertion device (200) includes a shaft (206) having distal and proximal end portions (208, 210) and a plurality of lumens (212, 214). A first lumen (212) is configured to receive a guidewire and a second lumen (214) is configured to receive a pressurized fluid. A tip (220) connected to the distal end portion (208) of the shaft (206) is configured for insertion into the heart chamber. The tip (220) has a hollow interior (226) communicating with the first shaft lumen (212). An inflatable member (224) is coupled to the distal end portion (208) of the shaft (206) and includes a hollow interior (254) in fluid communication with the second shaft lumen (214). The inflatable member (224) is movable between deflated and inflated configurations for releasably ...

DRAINAGE CATHETER

A medical catheter inserted into a body cavity for drainage of fluid. The catheter comprises flexible fibers/filaments that form a plurality of channels for movement of fluid. These fibers/filaments are located around a central inflation device contained within a flexible tubular catheter, composed of two parts. The outer sleeve and inner sleeve form a tubular catheter joined by a flexible connector that interlocks the sleeves during insertion. Once inserted the connection between the two sleeves is released, enabling the outer sleeve to move over top of the inner sleeve revealing fibers/filaments for fluid drainage. An inflatable retention balloon contained within the fibers/filaments secures the catheter in the bladder once inflated. This arrangement allows insertion of non-contaminated fibers/filaments into the body cavity. Insertion of these fibers/filaments creates a more complete drainage of fluid, decreased risk of bacterial infection, reduction of blockage, and improved patient ...

AUTORETROPERFUSION DEVICES, SYSTEMS, AND METHODS FOR ACHIEVING VENOUS ARTERIALIZATION

Devices, systems, and methods for providing retroperfusion to at least one ischemic tissue in a minimally invasive manner are disclosed. At least some of the embodiments disclosed herein enable an anastomosis to be formed between a vein and an artery without the use of sutures and through a non-invasive procedure. In addition, various disclosed embodiments provide a cannula device comprising a Y-configuration for bifurcating arterial flow between an anastomosis and the underlying artery. The devices, systems and methods herein can further provide simultaneous autoretroperfusion therapy to more than one area of an ischemic tissue.

FETAL ELECTRODE APPLICATOR APPARATUS

A fetal electrode applicator for attaching a coil electrode to the skin of a fetus by moving the coil electrode forwardly through the forward end of an inserter tube introduced through the mother's vagina by means of a plunger includes cooperating helical thread-type means for converting linear force applied to the plunger to rotary motion of the coil electrode. In one embodiment, the helical thread-type means includes cooperating helical ribs and grooves on the electrode carrier and the forward interior wall of the inserter tube, and a plunger rod pushes the electrode carrier forwardly. In the preferred embodiment, helical grooves are formed on a motion converter which carries the electrode carrier, and radially-inwardly projecting pins on the forward interior wall of a plunger tube engage the helical grooves; and stop means are provided for limiting forward movement of the motion converter, whereby depression of the plunger after the coil electrode has moved forwardly a predetermined ...

GASTROSTOMY TUBE EXTENSION DEVICE

To provide a gastrostomy tube extension device which can facilitate the insertion or removal operation in and from the patient, as well as to increase the simplicity of manufacture without sacrificing safety of operation. [Solving Means] A gastrostomy tube extension device 20 used for inserting or taking out the gastrostomy tube 10 into/from the hole on the patient includes a rod 21, a fixing member 22, and an engaging member 23. The rod 21 is formed of a rod-shaped member, and is formed with engaging stepped portions 24a on the proximal portion thereof. The fixing member 22 is adapted to be capable of moving along the longitudinal direction of the rod 21, and an engaging projection 35 which can be fixed to the tube member 11 is formed on the peripheral surface of the fixing member 22. The engaging member 23 includes a lower engaging portion 26 engageable with the engaging projection 35 and an upper engaging portion 27 which is engageable with the engaging stepped portion 24a. This assembly ...

INJECTION APPARATUS

The present invention relates to an apparatus and method for using the apparatus for injecting an agent into a tissue, particularly into thin tissues such as the sclera of the eye. The invention provides an apparatus and method for effectively imbedding a needle into a tissue at a predetermined penetration approach angle and penetration distance thereby reducing the risk of penetrating the full thickness of the tissue. The invention includes a support element and a needle guide platform disposed on the support element with an external support surface and a channel extending therethrough and terminating in an aperture at the support surface. A needle disposed in the channel is axially movable along an axis of injection through the channel. The needle is movable from a first retracted position to an extended position corresponding to the penetration distance, along the axis of injection. In one aspect, the needle includes a sidewall defining an outlet in the needle such that when an agent ...

DEVICES AND METHODS FOR PERCUTANEOUS INTRATUMORAL THERAPY DELIVERY

Percutaneous therapy or drug delivery devices are described herein. The device can include one or multiple lumens inside a cannula or catheter body. The device can include features for reducing or preventing backflow or reflux of infusate along the device insertion track, such as one or more bullet noses, over tubes, and/or micro-tips. The device can be used in any of a variety of treatment methods, including to inject cancer therapy medicinal products directly into pulmonary tumors or tumors located in other regions of the body. The device can include features to keep the distal tip secure during patient respiration or during other patient movement, and can reduce the incidence of reflux during therapy delivery.

IMPROVED SURGICAL CANNULAS

Disclosed herein are multiple cannulas defining a lumen sized and dimensioned to receive one or more medical instruments, an inflatable outer membrane attached to an outer surface of the cannula, and at least one activator that reversibly activates the cannulas to push a fluid contained in the cannulas into the outer membrane to fill or pressurize the outer membrane. Also disclosed are methods for operating these cannulas.

PRESSURE REGULATOR FOR CUFFED INTUBATION TUBE

Un régulateur de pression pour sonde d'intubation, canule de trachéotomie ou instrument similaire destiné à la ventilation d'un patient, l'instrument comportant un tuyau principal ayant une première extrémité destinée à être insérée dans la trachée artère d'un patient et une seconde extrémité destinée à être raccordée à un appareil respirateur, un ballonnet annulaire gonflable d'étanchéité, qui entoure la première extrémité du tuyau principal, et au moins un tuyau auxiliaire ayant une première extrémité raccordée au ballonnet d'étanchéité et une seconde extrémité munie d'une valve pouvant être raccordée à une source d'air comprimé pour le gonflage du ballonnet d'étanchéité. Le régulateur comprend un récipient définissant une chambre à volume variable ayant au moins un premier orifice pour être raccordé au tuyau auxiliaire et un moyen de pression agissant sur le récipient. Le régulateur comprend aussi un système de verrouillage de la masse pour éviter son déplacement inopiné.

CATHETER WITH BALLOON VALVE

A catheter having a selectively inflatable external balloon and an internal balloon, where the internal balloon is operable as a valve to control fluid flow through a channel.

APPARATUS FOR MAPPING AND COAGULATING SOFT TISSUE IN OR AROUND BODY ORIFICES

A probe that mays be used to create circumferential lesions in body tissue and, in some implementations, may also be used to perform mapping functions. The probe includes a collapsible/expandable structure that supports electrodes or other operative elements against the body tissue.

CATHETER DEVICE FOR THE CONTROL OF LIQUID DISCHARGE FROM THE URINARY BLADDER BY A USER PERSON

A catheter device for the control of liquid discharge from the urinary bladder, and its use, is described. The catheter device is an elongated flexible tube of elastic material having an inlet opening at a distal end thereof communicating with a discharge conduit of the tube. An elongated inflatable balloon or at least three spaced-apart balloons are secured about the tube spaced from the inlet opening. The balloon retains the catheter at a predetermined position within the urethra while preventing urine to flow about the catheter below the balloons. A plug is removably secured in a discharge end of the discharge conduit for a user person to discharge urine from the bladder.

NEEDLE HUB FOR OVER-THE-NEEDLE CATHETER

The present disclosure is directed to an over-the-needle (OTN) catheter assembly having an improved needle hub. The OTN catheter assembly includes a catheter defining a lumen extending from a proximal end to a distal end. A needle having a proximal end and a distal end is configured within the lumen of the catheter. The needle hub is configured with the proximal end of the needle and includes a bore defined therethrough. The needle hub also includes at least one cavity extending from the bore to an exterior surface of the needle hub. Thus, the needle extends at least partially through the bore of the needle hub such that the needle is exposed via the cavity from the exterior surface of the needle hub so as to engage a nerve stimulator apparatus.

TEMPERATURE SENSING CATHETER

An improved catheter is described. The catheter may have an inflation lumen reinforced with a metal support, such as a coil, to prevent collapse and deflation of the inflation lumen, while leaving a minimal impact on the size of the catheter. The catheter may be manufactured with a temperature sensing strip permanently integrated into the catheter during the manufacturing process. The temperature sensing strip is able to wirelessly send information regarding a patient's temperature to an external display, where it may be available for viewing by a care provider. Additionally, the drainage lumen of the catheter is preferably coated with a hydrophobic coating or treatment, and/or formed to include a patterned microstructure surface design, such as superhydrophobic patterned surface.

SYSTEMS AND METHODS FOR REDUCING PRESSURE AT AN OUTFLOW OF A DUCT

Various systems and methods are provided for reducing pressure at an outflow of a duct such as the thoracic duct or the lymphatic duct. In one embodiment, an indwelling catheter can be configured to be at least partially implanted within a vein of a patient in the vicinity of an outflow port of a duct of the lymphatic system. The catheter can include first and second restrictors each configured to at least partially occlude the vein within which the catheter is implanted and thus to restrict fluid flow within the vein when the restrictors are activated. The restrictors can each be configured to move between an activated configuration, in which the restrictor occludes the vein, and a relaxed configuration, in which the restrictor does not occlude the vein. The catheter can include a pump, such as an axial motor pump, configured to pump fluid through the catheter.

PULMONARY-VEIN CORK DEVICE WITH ABLATION GUIDING TRENCH

A method includes inserting into a patient body a catheter, which includes an insertion tube and at least an expandable distal-end device coupled to a distal end of the insertion tube. The distal-end device is expanded in a blood vessel, thereby forming an annular guiding trench between the distal-end device and a circumference of the blood vessel, the annular trench shaped to receive and guide a distal tip of a medical instrument. The distal tip of the medical instrument is guided in the annular guiding trench formed by the expanded distal-end device of the catheter, so as to approach multiple points on the circumference of the blood vessel.

CANNULA DEVICE, ARTIFICIAL LUNG

Dispositif de canule (1) pour la circulation du sang dans un poumon artificiel caractérisé en ce qu'il comprend : - une première lumière (LA), dite lumière d'aspiration, comprenant au moins un orifice permettant l'aspiration d'un volume de sang; - une seconde lumière (Ll), dite lumière d'injection, comprenant au moins un orifice permettant l'injection d'un volume de sang, caractérisée en ce que la lumière d'injection (Ll) et la lumière d'aspiration (LA) sont maintenues solidaire sur au moins une portion de leur longueur, lesdites lumières étant étanches l'une de l'autre, la lumière d'injection (Ll) comportant un élément déformable (STN) maintenu sur une portion de son extrémité distale, ledit élément déformable (STN) comportant un premier agencement dit de « passage » et un second agencement dit « de maintien », le passage du premier agencement au second agencement s'effectuant par une modification du diamètre dudit élément déformable (STN).

SYSTEM FOR RE-ENTERING A VESSEL LUMEN

This disclosure is directed to systems and methods for re-entering the true lumen of a vessel. The re-entry catheters (10) employ deflectable struts (20) to stabilize and support the distal tip (16) in a subintimal location while a passageway back into the true lumen is formed. Re-entry to the true lumen can be effected with a cutting element or with a conventional guidewire.

CATHETER CURVATURE BRACES AND METHODS OF USING SAME

A catheter curvature brace, catheter assembly and method for managing fluid in a patient, the brace being attachable to a distal portion of a shaft of a catheter and having an elongated frame with a distal end and a proximal end. The frame is formed with at least one curve in a relaxed curved configuration. At least two coupling elements are connected to the frame, each coupling element configured to engage an outer surface of the catheter. At least the frame is formed of an elastic, biocompatible material capable of being straightened by a force and then returning to the relaxed curved configuration after the force is removed, thereby bending the catheter to substantially conform to the relaxed curved configuration.

CATHETER CURVATURE BRACES AND METHODS OF USING SAME

A catheter curvature brace, catheter assembly and method for managing fluid in a patient, the brace being attachable to a distal portion of a shaft of a catheter and having an elongated frame with a distal end and a proximal end. The frame is formed with at least one curve in a relaxed curved configuration. At least two coupling elements are connected to the frame, each coupling element configured to engage an outer surface of the catheter. At least the frame is formed of an elastic, biocompatible material capable of being straightened by a force and then returning to the relaxed curved configuration after the force is removed, thereby bending the catheter to substantially conform to the relaxed curved configuration.

APPARATUS FOR PREVENTING OVER INFLATION OF THE RETENTION BALLOON IN MEDICAL CATHETERS AND AIRWAY DEVICES

The body has a fluid inlet port for receiving pressurized fluid and a fluid outlet port connected to the retention balloon. A first passage connects the fluid inlet port and the fluid outlet port, A second passage in the body is connected to the balloon fluid return path and is at the pressure of the retention balloon. A. valve prevents fluid flow through the first passage when actuated. The valve includes a pressure-responsive member movable to a position to obstruct fluid flow in response to fluid pressure in the second passage exceeding the predetermined level. Flexible means such as a membrane defines a normally open portion of the first fluid passage, which is closed by the moveable means bearing on the membrane when pressure exceeding the predetermined level actuates the valve.

INDWELLING STENT AND METHOD OF USE

A stent (21) is disclosed having a pigtail (33) at its distal end (35) and having a flap (23) acting as a barb at its proximal end (29). Stent (21) includes a catheter body (31) having at least one lumen (43) and having drainage holes (37, 39). The stent may be made of radiopaque polyethylene. The pigtail (33) prevents entire proxima l migration of catheter body (31) while allowing spring action to accommodate variations in length, while flap (23) prevents entire distal migration while being radially retractable to facilitate insertion. An alternative embodiment is disclosed having multiple flaps (25, 27) acting as a barb. A method of use is also disclosed.

APPARATUS AND METHOD FOR LOCATING A BREAST MASS

... 2125674 9311827 PCTABS00022 A mass localization device (10) includes a catheter (12) and a needle (30). In one embodiment, the catheter includes inner (18) and outer (20) walls spaced from each other and creating a gap (22) between the walls extending along substantially the entire lenth of the catheter. The distal portion of the outer wall includes an inflatable balloon (28). In use, the balloon is positioned proximate the mass and inflated to make the mass palpable. An incision to the mass can be achieved by the shortest possible distance since the mass is made palpable.

Anchor Systems and Methods

Some embodiments of a medical device anchor system include an anchor device that receives a medical instrument (such as a catheter or the like) and secures the instrument in place relative to a skin penetration point. In some circumstances, the anchor device may allow the anchor device to be used after medical instrument is already in place without the need for a second penetration point for the anchor device.

Medical tubing stabilizer

In various embodiments of the invention, a system and dynamic device are provided to create stability of tube placement in medical and other applications. The described systems and principles also apply in other environments outside of medicine and healthcare. The described medical tubing stabilizer adheres to the tubing itself providing handles or anchors to prevent stitch slippage and to prevent the tubing from falling out in any situation that requires a semi or permanent tubing placement. The device also aides in stabilizing the tubing in the wound site, and thus maximizes placement in its intended area of effect (e.g., in the body cavity, in a medical context). These stabilizing effects substantially minimize slippage of stitching holding the tubing in place to prevent the tubing from falling out or becoming dislodged or displace, thus preventing irritation and damage to the skin around the wound site, infection, seroma, edema and morbidity in a medical context.

Method and Apparatus for Delivering a Lead to a Heart

A method and apparatus for creating and accessing an anatomic space between a heart and a pericardial sac. The apparatus includes a catheter having a cryoadhesion member situated on the distal tip of the catheter. The cryoadhesion member is utilized to adhere to the pericardial sac and to retract the sac to create a tent like structure. The catheter allows introduction of an instrument to access the pericardial sac by puncture. The access to the pericardial sac allows delivery of a device, a drug, a biologic or other substance to the heart or the space around the heart.

Securement device

A securement device includes a filament which passes underneath at least a portion of the securement device and can be secured about a medical article to be retained. The filament may be secured about the medical article without the use of adhesive. At least a portion of the securement device underlying the medical article may comprise a compressible material which may be used to exert a restoring force upon the medical article to hold the medical article tightly in place.

Intravenous catheter anchoring device

An intravenous catheter anchoring assembly is disclosed and includes a patient-contacting membrane, a platform, and a retaining strap for securing a catheter or tubing of an administration set to a patient. The strap is attached to the platform with adjustable pull-tabs that permit a variety of catheter shapes and sizes to be secured. The strap is also elastomeric so that the strap is stretchable and thereby grabs the secured catheter. The strap and platform further define a plurality of passageways that permit the catheter to be secured in a plurality of non-aligned directions.

Endotracheal intubation device

A stylet assembly for performing a nasal endotracheal intubation of a patient is disclosed. The stylet assembly includes an elongated tube as a stylet for the intubation defining a longitudinal axis, a proximal end, and a distal end for entering the trachea of the patient. The elongated tube includes (i) a rigid section adjacent the proximal end, (ii) an articulation section adjacent the distal end and adapted to curve into the patient's trachea upon actuation, and (iii) a flexible section between the rigid section and the articulation section, the flexible section being adapted to curve to an internal shape of at least one of the patient's nose, nasal cavity, pharynx, and larynx during nasal intubation. The stylet assembly can further include an actuator housing, a control wire for actuating the articulating section, and a hand grip for maneuvering the stylet assembly.

Healthcare Form Assembly Having a Plurality of Removable Strips with Adhesive Free Feature

A healthcare treatment form assembly suitable for use in a patient treatment theater for use in securing treatment appliances to an individual. The form assembly includes a laminated, pressure sensitive assembly having a plurality of uniquely sized strips that can be easily removed and applied by the care giver.

Catheter with coronary sinus ostium anchor

A method of treating cardiac tissue is provided, including positioning a first chamber of a medical device adjacent an atrial wall; directing a cryogenic coolant into the first chamber; anchoring the first chamber to the atrial wall through cryoadhesion; directing a distal portion of the medical device into the coronary sinus; and positioning a cardiac lead through at least a portion of the coronary sinus with the distal portion. The method may include measuring a temperature of the first chamber; removing the first chamber from the atrial wall once a predetermined threshold temperature of the first chamber is reached; anchoring a second chamber of the medical device to a portion of the coronary sinus; and/or perfusing blood flow through at least a portion of the second chamber.

Specialized catheter securement devices for peripherally inserted central catheters

A catheter securement device in accordance with the present invention includes a flexible base member having an adhesive side and an opposite non-adhesive side. A single piece elastomeric anchoring member is mounted on the non-adhesive side of the base member. The anchoring member integrally includes a pair of opposing pull tabs, a slit disposed between the opposing pull tabs, and a third pull tab disposed between the slit and one of the opposing pull tabs. Pulling the opposing pull tabs opens the slit for receiving a catheter hub in the slit, and the third pull tab is insertable into the slit for securing the catheter hub between the anchoring member and the base member.

Biliary Catheter Systems Including Stabilizing Members

Medical devices including devices and systems for endoscopic interventions that may access the biliary tree. An example biliary catheter system may include an endoscope having a working channel formed therein. An endoscopic instrument may be disposed in the channel. The endoscopic instrument may have a tool channel formed therein, a distal end, and a plurality of stabilizing members extending from the distal end. The plurality of stabilizing members may be configured to surround the ampulla of Vater during a biliary tract intervention.

Antimicrobial Dressing Providing Percutaneous Device Securement and Cover

The present invention is related to a polymeric vehicle for delivery of bioactive agents, and preferably, for the delivery of one or more bioactive agents. The invention is also directed to a percutaneous device securing and drug delivery device comprising, as a component thereof, a material which delivers antimicrobial and/or other wound-healing factors at the site of the insertion of the catheter into the body. The device, when applied as described herein, provides complete anti-microbial coverage around the entry point of a percutaneous device and, preferably for a length greater than the diameter of the device. The present invention is also directed to methods for using such devices in combination with percutaneous devices primarily to reduce site infections.

Method for accessing the left atrial appendage with a balloon-tipped transseptal sheath

A method for accessing the left atrial appendage with a balloon-tipped transseptal sheath is disclosed. A transseptal sheath is delivered to the left atrium through the intraatrial septum from the right atrium. The balloon tip may be inflated to prevent the transseptal sheath from falling proximally into the right atrium. The inflated balloon tip permits safe probing and exploration of the left atrial appendage and facilitates safe maintenance of the position of the transseptal sheath within the left atrial appendage while delivering an implantable device to the left atrial appendage.

Catheter For Reduced Reflux in Targeted Tissue Delivery of a Therapeutic Agent

A therapeutic agent delivery system that includes a catheter having a proximal end and an opposite distal end. The catheter has a body with a lumen defined therein. The body of the catheter includes a non-bulbous region having a substantially uniform outer diameter and a bulbous region made from an elastically deformable material. While in a first state the bulbous region has a maximum outer diameter greater than the substantially uniform outer diameter of the non-bulbous region; and while in a second state the maximum outer diameter of the bulbous region is reduced relative to that while in the first state.

Anchoring a Medical Instrument

Some embodiments of a medical anchor device include an elongate body coupled with deployable subcutaneous anchors to secure a catheter instrument (or other medical instrument) in place relative to a skin penetration point. In some circumstances, the elongate body may be in the form of catheter hub body, and the subcutaneous anchors can be deployed from the hub body by adjustment of a movable actuator. A locking member can interact with the actuator so as to retain the actuator in the deployed orientation during the medical procedure.

Methods and devices to curb appetite and/or reduce food intake

The present invention relates to methods and devices that help to curb appetite and/or reduce food intake. In one embodiment, the methods and devices of the present invention include a small intestinal/duodenal insert comprising an elongated member with at least one flow reduction element that can cause the stimulation of one or more biological signals of satiety.

Medical article securement device

A medical article securement device 100 holds a medical article 300 such as a catheter hub or a connector fitting in position upon the body of a patient and inhibits movement of the medical article relative to the patient. The medical article 300 includes an elongated body 430 , a pair of outwardly extending wings 301 ( a ), 301 ( b ), and a port 305 . The securement device 100 includes a retainer 120 and at least one anchor pad 110 . The retainer 120 forms a channel 140 into which at least a portion of the medical article 300 is secured. The retainer 120 includes at least one abutment that abuts against a contact point or surface on the port 305 . The anchor pad 110 includes an adhesive layer that is attached to both an epidural layer of a patient and at least a portion of the pair of wings 301 ( a ), 301 ( b ).

Systems and methods for engaging heart tissue

A system for engaging heart tissue includes an engagement catheter defining a first lumen therethrough and having a suction port at or near a distal end and a vacuum port at or near a proximal end, a delivery catheter defining a delivery catheter lumen therethrough and configured for slidable insertion into the first lumen of the engagement catheter, and an implantable device capable of insertion into the delivery catheter lumen such that at least part of the implantable device extends from a delivery catheter distal end upon implantation into a patient, where the suction port is operable to removably attach to a targeted tissue on an interior wall of a heart of the patient after the engagement catheter has been advanced through a blood vessel and into the heart, thereby forming a reversible seal with the targeted tissue when a vacuum source is operatively coupled to the vacuum port.

Wound dressing system

System, method, and components for hygienic maintenance of a surgical wound configured for drainage of ascites from a body cavity. Different aspects of the system may include one or more of a wound dressing, a pocket for low-profile, hygienic, and aesthetic storage of a drainage catheter configured for attachment to a patient and/or wound dressing, and an apron device configured for installation and/or exchange of a wound dressing.

Fetal shunt

A medical device, system, and method are described for treating in utero a fetus with a lower urinary tract obstruction. An implantable medical device may have a flexible catheter and an anchor. The catheter may define a proximal port, a distal port, a longitudinal axis, and a lumen providing fluid communication between the ports. The anchor may be affixed to the catheter at a position between the ports, and may have a resilient proximal member and a resilient distal member spaced a longitudinal distance apart, the proximal member and distal member each extending radially outward with respect to the longitudinal axis. An elongate delivery member may be releasably affixed to the medical device, and the medical device may be delivered through a tubular sheath defining a sheath lumen.

Vacuum assisted percutaneous appliance

A device for reducing agent penetration at an insertion site is provided that has a porous inner sleeve fluidly connected to a conduit. A vacuum or hydrodynamic source is fluidly connected to the conduit. The device is stabilized by fibroblast in-growth and inhibits bacterial colonization. A device is also provided that has a conduit having a bore and an outer conduit surface. The outer conduit surface is optionally nanotextured to promote fibroblast adhesion and limit bacterial residency. A sleeve is provided in fluid communication with the bore of the conduit, and is formed from materials characterized by a pore matrix through which vacuum or hydrodynamic draw is achieved in a process to promote stabilization and reducing bacterial colonization by draw fluid from an area around the surrounding the site of the device. The sleeve optionally has a distal nanotextured surface.

Naso/orogastric tube having one or more backflow blocking elements, backflow blocking elements, and a method of using backflow blocking elements

A naso/orogastric device that comprises a naso/orogastric tube sized and shaped for being disposed within the esophagus so that at least a distal segment thereof being placed in the stomach lumen of a patient and at least one self expending element disposed around a peripheral surface of the naso/orogastric tube and having a first thickness in a compressed state and a second thickness in an expanded state, the at least one self expending element switching from the compressed state to the expanded state when absorbing moisture. The first thickness is thinner than the second thickness.

Protective dressing and methods of use thereof

A protective device having a substantially rigid casing for placement on a patient's skin, wherein the casing has a hollow interior facing the patient's skin and a lip. The casing can be spanned across its hollow interior by a membrane. The casing can have a first adhesive seal attached to a bottom surface of the lip of the casing, and a second adhesive seal attached to the top surface of the lip of the casing.

Device for guiding perfusion tube(s)

A device for guiding perfusion tube(s) ( 10 ), includes a wrist strap ( 11 ) with a closing member ( 14 ) so that it can be secured to a limb of a patient and bearing a guiding plate ( 12 ) for at least one perfusion tube ( 5, 6 ). The device is characterized in that the guiding plate ( 12 ) includes, in the body thereof, at least one first substantially U-shaped guiding groove ( 16 ) of a tube ( 5 ) and a second substantially straight guiding groove ( 17 ) extending in the longitudinal direction of the wrist strap ( 11 ) and arranged tangentially to the first guiding groove ( 16 ) so that a tube ( 5 ) can be partially arranged in one of the first guiding grooves and partially in the other guiding groove.

SYSTEM FOR ANCHORING MEDICAL DEVICES

Some embodiments of a medical device anchor system include an anchor device that receives a catheter (or other medical instrument) and secures the catheter in place relative to a skin penetration point. In some embodiments, the anchor device can secure the catheter in an operative position relative to the skin without the use of sutures or skin tapes. In particular embodiments, the anchor device can be adjusted to a folded condition so that subcutaneous anchors are partially rotated prior to removal from the skin penetration point. 1. A method of using a catheter anchor device , comprising:advancing a catheter though a skin penetration point;directing an anchor device toward the skin penetration point that is occupied by a portion of the catheter, the anchor device comprising: a retainer body to releasably couple to an external portion of the catheter arranged outside the body, and first and second anchors extending distally of a distalmost face the retainer body;inserting the first and second anchors through the skin penetration point that is occupied by the catheter so that at least a portion of the first and second anchors are deployed in a subcutaneous region proximate the skin penetration point;securing the catheter with the retainer body so that the catheter is anchored relative to the skin penetration point;pivoting the first and second anchors about a longitudinal hinge region defined by the retainer body while first and second body portions of the retainer body on opposing sides of the longitudinal fold line remain physically coupled to one another so that the first and second anchors are adjusted from a deployed configuration to a removal configuration; andremoving the first and second anchors from the subcutaneous region and the skin penetration point.2. The method of claim 1 , wherein the step of pivoting the first and second anchors comprises pivoting the first body portion of the retainer body relative to the second body portion of the retainer body ...

ARTICULATING CRANIAL BOLT

A catheter guiding device includes a bolt including a shaft configured to be inserted within a hole drilled in a bone and a passageway extending longitudinally therethrough along a bolt axis and a guide member received within the passageway of the bolt and extending longitudinally along a guide axis. The guide member includes a guide channel extending therethrough along the guide axis, wherein, in a first configuration, the guide member is arrangeable to a desired position relative to the bolt to align the guide axis with a target area and, in a second configuration, the guide member is fixed in the desired position relative to the bolt such that the guide axis is at a desired angle relative to the bolt axis within a permitted range of angulations. 1. A catheter guiding device , comprising:a bolt including a shaft configured to be inserted within a hole drilled in a bone and a passageway extending longitudinally therethrough along a bolt axis; anda guide member received within the passageway of the bolt and extending longitudinally along a guide axis, the guide member including a guide channel extending therethrough along the guide axis, wherein, in a first configuration, the guide member is arrangeable to a desired position relative to the bolt to align the guide axis with a target area and, in a second configuration, the guide member is fixed in the desired position relative to the bolt such that the guide axis is at a desired angle relative to the bolt axis within a permitted range of angulations.2. The device according to claim 1 , the shaft of the bolt including a threading therealong to engage the hole drilled in the bone.3. The device according to claim 1 , the bolt including a head portion at a proximal end thereof sized and shaped to be engaged by a driving tool.4. The device according to claim 1 , wherein the passageway of the bolt includes a proximal portion which tapers radially inward from a proximal end thereof towards a distal end thereof and a distal ...

SYSTEM FOR ANCHORING MEDICAL DEVICES

Some embodiments of a medical device anchor system include an anchor device that receives a catheter (or other medical instrument) and secures the catheter in place relative to a skin penetration point. In some embodiments, the anchor device can secure the catheter in an operative position relative to the skin without the use of sutures or skin tapes. In particular embodiments, the anchor device can be adjusted to a folded condition so that subcutaneous anchors are partially rotated prior to removal from the skin penetration point. 1. An anchor system for securing the position of a medical instrument , comprising:a delivery device to advance an anchor device toward a skin penetration point that is occupied by a medical instrument, the delivery device defining an internal space and a distal opening; andthe anchor device being deployable from the internal space of the delivery device and comprising: a retainer base to releasably secure with the medical instrument, and one or more subcutaneous anchors that extend distally from the retainer base and toward the skin penetration point when the delivery device deploys the one or more subcutaneous anchors from the distal opening, each anchor comprising a tine that deploys in a subcutaneous region to secure the retainer base relative to the skin penetration point, wherein each tine is pivotable about a longitudinal axis from a deployed configuration to a removal configuration.2. The anchor system of claim 1 , wherein the retainer base is separable from the delivery device when the delivery device deploys the one or more subcutaneous anchors from the distal opening.3. The anchor system of claim 1 , wherein the one or more anchors extend distally from the retainer base such that the retainer base is arranged external to the skin penetration point when the tine is deployed in the subcutaneous region.4. The anchor system of claim 1 , wherein a first body portion of the retainer base is pivotable about a fold line relative to a ...

MEDICAL SECUREMENT DEVICE WITH TIMER

A medical article, such as an anchor pad for stabilizing a medical line and/or a medical line securement device to a patient's skin, is provided with a timer. The timer can measure and provide an indication of elapsed time. The timer can be flexible or rigid, and can be disposed directly on the anchor pad, on a flexible or rigid substrate disposed on the anchor pad, or on a retainer supported by the anchor pad. The anchor pad with integral timer provides an easy-to-use visual indicator of elapsed time since placement of the medical line, offering a reliable way to signal when the medical line should be re-sited. 1. An anchor pad for securing to a patient , the anchor pad comprising a timer.2. The anchor pad of claim 1 , wherein the timer is user activated.3. The anchor pad of claim 1 , wherein the timer provides an indication of elapsed time.4. The anchor pad of claim 3 , wherein the indication provided by the timer is visual.5. The anchor pad of claim 3 , wherein the indication provided by the timer is audible.6. The anchor pad of further comprising a display.7. The anchor pad of further comprising a protective layer covering at least a portion of the timer.8. The anchor pad of further comprising a chemical reservoir and a chemically active region.9. The anchor pad of further comprising a breakable barrier disposed between the chemical reservoir and the chemically active region.10. A securement system for securing a medical article to the skin of a patient claim 8 , the securement system comprising:an anchor pad having a lower surface, at least a portion of the lower surface being covered by an adhesive;a retainer supported by the anchor pad, the retainer being configured to receive at least a portion of the medical article; anda timer.11. The securement system of claim 10 , wherein the timer is disposed on the retainer.12. The securement system of claim 10 , wherein the timer indicates elapsed time.13. The securement system of claim 10 , wherein the timer is ...

Catheter Advancement

The present subject disclosure addresses the problems described herein by incorporating an extension in a catheter assembly for partitioning excess material of a sheath from an opening of a guide adapted to receive the catheter, thereby preventing the sheath from being pulled into the guide. Preventing the excess material from being pulled into the opening as the sheath is bunched up alleviates the difficulties of pushing the catheter through the opening. 1. A urinary catheter assembly , the assembly comprising:a catheter having a proximal end and a distal end;a guide adapted to receive the proximal end of the catheter via an opening;a sheath surrounding a substantial portion of the catheter, wherein a proximal end of the sheath is attached to the guide; anda hollow extension attached to a distal end of the guide, the hollow extension being enclosed by the sheath and being placed in between the sheath and the opening.2. The assembly of claim 1 , wherein the extension has a greater distal diameter than a proximal diameter.3. The assembly of claim 2 , wherein the extension is in the form of a cone.4. The assembly of claim 2 , wherein the extension is in the form of a hemisphere.5. The assembly of claim 1 , wherein the extension maintains a substantially similar shape during catheter insertion.6. The assembly of claim 1 , wherein the extension and the guide are made from a substantially similar material.7. The assembly of claim 1 , wherein the proximal end of the guide is connected to a reservoir including a lubricant for lubricating the catheter as it moves through the reservoir.8. An extension for a urinary catheter assembly claim 1 , the extension comprising:a hollow member; andan attachment portion at a proximal end of the hollow member, the attachment portion attachable to a distal end of a guide adapted to receive a catheter;wherein the hollow member is in between the catheter and a sheath substantially surrounding the catheter when attached to the distal end of ...

Catheter Reservoir Seal

A reservoir is incorporated in between a guide portion and an introducer tip of the introducer member. A spherical or similarly shaped plug is inserted into the guide portion. The plug is designed such that it forms a seal within the guide portion, preventing any fluid flow between the reservoir and an environment external to a distal end of the guide portion. This prevents a liquid or gel contained inside the reservoir from drying or leaking. The plug may further be held in place against a distal opening of the reservoir by positive pressure within the reservoir. The plug may further be held in place within the guide portion by a plurality of bumps or notches. When the catheter is advanced through the guide portion, the catheter tip pushes the plug into the reservoir, thereby breaking the seal and lubricating the catheter. 1. An introducer member for a urinary catheter assembly , the introducer member comprising:a proximal end being adapted for urethral insertion;a distal end for receiving a catheter;a throughbore extending from a first opening at said proximal end to a second opening at said distal end;a reservoir portion disposed within said throughbore, the reservoir portion including a lubricant; anda plug placed in between the reservoir portion and the second opening, the plug providing a seal between the reservoir portion and an environment external to the second opening.2. The introducer member of claim 1 , wherein the plug is adapted to move into the reservoir portion when pushed by the catheter during catheter advancement.3. The introducer member of claim 1 , wherein the plug provides an airtight seal within the throughbore between the reservoir portion and the second opening.4. The introducer member of claim 3 , wherein the plug is held in place by a plurality of projections extending inward from an inner wall of the throughbore between the reservoir portion and the second opening.5. The introducer member of claim 4 , wherein the plurality of projections ...

SYSTEMS AND METHODS FOR ANCHORING MEDICAL DEVICES

Some embodiments of a medical device anchor system include an anchor device that secures a medical instrument (such as a catheter or the like) in place relative to a skin penetration point using subcutaneous anchors. In some implementations, the anchor device can be installed using a technique in which the subcutaneous anchors undergo relatively little or no flexing when being inserted through the skin into the subcutaneous region between the skin and underlying muscle tissue which may be occupied by fatty tissue. 1. An anchor device for releasably securing to an external portion of a catheter while another portion of the catheter occupies a skin penetration point , the anchor device comprising:first and second anchors each having a longitudinal shaft portion and a flexible subcutaneous tine configured to be deployed through the skin penetration point and into a subcutaneous region along an underside of a skin layer; anda retainer base to releasably secure with the external portion of the catheter, the retainer base being in a folded condition about a longitudinal fold axis of the retainer base prior to deployment of the flexible subcutaneous tines through the skin penetration point such that the flexible subcutaneous tines are positioned generally adjacent to each other and oriented to extend in substantially the same direction, wherein the longitudinal shaft portion the first anchor is positioned on an opposite side the longitudinal fold axis from the longitudinal shaft portion the second anchor, and wherein the longitudinal shaft portion of each of the first and second anchors extends distally in a longitudinal direction from a distalmost end of the retainer base,wherein the retainer base is adjustable to a non-folded condition about the longitudinal fold axis of the retainer base after deployment of the flexible subcutaneous tines through the skin penetration point so that the flexible subcutaneous tines are in an anchored position in which the flexible ...

MEDICAL APPLIANCE SECURING DEVICE AND METHOD OF USING THE SAME

Medical appliance securing device and method of using the same to secure a medical appliance to a patient. In one embodiment, the device may be used to secure a hemodialysis catheter to a patient and may include a first base portion, a first adhesive for securing the first base portion to an object, such as a patient, the first adhesive being positioned under and coupled to the first base portion, a second base portion, the second base portion being positionable over the first base portion and fastenable to the first base portion; and a strap, the strap having a first end coupled to the first base portion and a second end fastenable to the second base portion. 1. A medical appliance securing device comprising:(a) a first base portion;(b) a first adhesive for securing the first base portion to an object, the first adhesive being positioned under and coupled to the first base portion;(c) a second base portion, the second base portion being positionable over the first base portion and fastenable to the first base portion; and(d) a strap, the strap having a first end coupled to the first base portion and a second end fastenable to the second base portion.2. The medical appliance securing device as claimed in wherein the first base portion and the second base portion constitute two separate pieces of material.3. The medical appliance securing device as claimed in wherein the first base portion and the second base portion constitute two parts of a single piece of material.4. The medical appliance securing device as claimed in wherein the first base portion and the strap constitute two parts of a single piece of material.5. The medical appliance securing device as claimed in wherein the first base portion claim 1 , the second base portion claim 1 , and the strap constitute three parts of a single piece of material.6. The medical appliance securing device as claimed in wherein at least one of the first base portion claim 1 , the second base portion claim 1 , and the third ...

PROTECTIVE WOUND SHIELD

A light-weight, semi-rigid wound shield protects wounds and intradermal therapy ports from impacts between therapy sessions. The wound shield comprises a domed cover forming a concave cavity above the wound or therapy port. A flange surrounding the cavity presses against the patient's skin to deflect and distribute the force of impacts. The flange may include a self-adhesive layer on its bottom, or it may be secured with medical tape or a fitted bandage that overlaps the flange and the surrounding skin. A peel-away membrane covers the adhesive layers. A tunnel through the flange may connect to the cavity to accommodate a therapy tube which remains in place while the shield is worn. In an alternate embodiment, a base coextensive with the flange adheres to the patient's skin and the wound shield removably couples to the base by its flange. The assembly comes in a sterile envelope or package. 1. A protective wound shield for covering a wound site on a patient's skin , said shield having a longitudinal major shield axis and a transverse minor shield axis and comprisinga flange having a flange bottom surface and an opposite flange top surface, said flange further having a flange outer perimeter surrounding a flange inner margin adapted to surround said wound site;a concave dome having a dome margin coupled to said flange inner margin and spanning said wound site to define an interior shield cavity; andadhesive means for adhering said wound shield to said patient's skin.2. The protective wound shield of wherein said adhesive means comprisesan adhesive layer disposed on at least a portion of said flange bottom surface.3. The protective wound shield of wherein said adhesive means comprisesa bandage adapted to at least partially surround said dome margin and to overlap said flange and said patient's skin, said bandage having a bandage lower surface bearing an adhesive layer adapted to adhere to both of said flange top surface and said patient's skin surrounding said flange ...

Zero-Pressure Balloon Catheter and Method for Using the Catheter

A safety catheter includes a shaft. The shaft has a proximal shaft portion having a proximal end, a distal tip portion defining a junction with the proximal shaft portion, a fluid drain lumen, and a balloon inflation lumen. The fluid drain lumen defines a distal fluid drain opening at the distal tip portion distal of the junction and a proximal fluid drain opening adjacent the proximal end and fluidically connected to the distal fluid drain opening. A hollow zero-pressure balloon is disposed at the junction and has an interior fluidly connected to the balloon inflation lumen, a distal leg fixedly secured to the distal tip portion, and a proximal leg temporarily secured to the proximal shaft portion. 1. A safety catheter , comprising: a proximal shaft portion having a proximal end and a distal end;', 'a distal tip portion defining a junction with the proximal shaft portion;', a distal fluid drain opening at the distal tip portion distal of the junction; and', 'a proximal fluid drain opening adjacent the proximal end and fluidically connected to the distal fluid drain opening; and, 'a fluid drain lumen defining, 'a balloon inflation lumen;, 'a shaft having an interior fluidly connected to the balloon inflation lumen;', 'a distal leg fixedly secured to the distal tip portion; and', 'a proximal leg temporarily secured to the proximal shaft portion., 'a hollow zero-pressure balloon disposed at the junction and having2. The safety catheter according to claim 1 , wherein:the proximal shaft portion adjacent the junction has a given outer diameter; anda portion of the junction adjacent the proximal shaft portion has an outer diameter less than the given outer diameter.3. The safety catheter according to claim 2 , wherein the distal tip portion adjacent the junction has an outer diameter one of:less than the given outer diameter;equal to the given outer diameter; andequal to the outer diameter of the junction.4. The safety catheter according to claim 1 , wherein:a proximal ...

Patient site protective cover

A patient site protective cover comprising a membrane, a resilient and substantially impermeable seal around a perimeter of the membrane and dimensioned to surround a site of a patient. At least one strap is operably coupled to the membrane and configured to secure the cover over the site.

METHOD FOR MANUFACTURING OF A TUBULAR OBJECT FOR INSERTION INTO A BODY PASSAGEWAY

Disclosed are a method and an apparatus for manufacturing a medical tubular object, such as a catheter, for insertion into a body passageway. The method comprises the steps of extruding a tube by pushing tube material though an extrusion nozzle and cutting the extruded tube at a predetermined length. Further, an initial part of the extruded tube is advanced onto a tapered mandrel arranged adjacent the extrusion nozzle such that a flared end is formed, and after a predetermined length of the extruded tube has been advanced onto the tapered mandrel, the tapered mandrel is moved away from the extrusion nozzle to prevent that the rest of the extruded tube is expanded by the tapered mandrel. 1. A method for manufacturing a medical tubular object for insertion into a body passageway , comprising the steps of:extruding a tube by pushing tube material though an extrusion nozzle; andcutting the extruded tube at a predetermined length, advancing an initial part of the extruded tube onto a tapered mandrel arranged adjacent the extrusion nozzle such that a flared end is formed; and', 'after a predetermined length of the extruded tube has been advanced onto the tapered mandrel, moving the tapered mandrel away from the extrusion nozzle to prevent that the rest of the extruded tube is expanded by the tapered mandrel., 'characterized in the steps of2. The method of claim 1 , wherein the medical tube object is a catheter.3. The method according to claim 1 , wherein the tapered mandrel is moved in a direction of the extrusion.4. The method according to claim 1 , wherein the tapered mandrel is moved at a speed that substantially corresponds to a speed at which the extruded tube is produced.5. The method according to claim 1 , comprising the further step of securing the flared end of the extruded tube at the tapered mandrel.6. The method according to claim 1 , wherein the tube material comprises at least one of monosaccharide claim 1 , disaccharide claim 1 , oligosaccharide and ...

Indwelling catheter probe incorporating proanthocyanidines

An indwelling catheter probe, wherein it incorporates, at its external and/or internal surface, an extract of containing proanthocyanidines applied either by adsorption, by absorption, by coating or by any other application process, namely any physico-chemical process, said catheter probe thus treated ensuring the prevention or inhibition of the formation of a bacterial biofilm at its surface. 1Vaccinium macrocarpon. An indwelling catheter probe , wherein it incorporates , at its external and/or internal surface , an extract of containing proanthocyanidines applied either by adsorption , by absorption , by coating or by any other application process , namely any physico-chemical process , said catheter probe thus treated ensuring the prevention or inhibition of the formation of a bacterial biofilm at its surface.2Vaccinium macrocarpon. A catheter probe according to claim 1 , wherein the extract of contains approximately between 16 and 30% in mass of proanthocyanidines.3Vaccinium macrocarpon. A catheter probe according to claim 2 , wherein the extract of comprises 18% in mass of proanthocyanidines.4Vaccinium macrocarpon. A catheter probe according to claim 2 , wherein the extract of comprises 20% in mass of proanthocyanidines.5Vaccinium macrocarpon. A catheter probe according to claim 2 , wherein the extract of comprises 26% in mass of proanthocyanidines.6Vaccinium macrocarpon. A catheter probe according to claim 2 , wherein the extract of comprises 30% in mass of proanthocyanidines.7. A preparation process for a catheter probe according to claim 1 , wherein:{'i': 'Vaccinium macrocarpon', 'the extract of is mixed in powder form with a suitable solvent such as water or other inert solvent,'}{'i': Vaccinium macrocarpon', 'Vaccinium macrocarpon, 'the probe and solution prepared using the extract are brought into mutual contact for at least 24 h at a temperature of 37° C. so as to enable the adsorption or other means (for example absorption or coating)of fixing the ...

Prevention of Bacterial Adherence and Growth in an Urological Implant

A medical device is disclosed, which comprises a functional unit (C) for permanent or temporary placement in the urogenital tract of a human or animal body. The functional unit has at least one electrically conducting portion. A power source (G) supplies a current to the electrically conducting portion after placement of the functional unit in the urogenital tract. In this manner, the growth of bacteria on the functional unit can be reduced. 1. A medical device comprising:a functional unit for permanent or temporary placement in the urogenital tract of a human or animal body, the functional unit having at least one electrically conducting portion; anda power source operable to supply a voltage and/or current to the electrically conducting portion after placement of the functional unit in the urogenital tract in a manner effective to reduce the growth of bacteria and/or encrustation on the functional unit.2. The device of claim 1 , wherein the power source is operable to supply said current in a manner to generate a surface current density between 10 nA/mmand 10′000 nA/mm2 between a surface of said functional unit and environmental body material.31. The device of claim 1 , wherein the power source is operable to supply said current as an alternating current with a frequency below kHz.4. The device of claim 1 , wherein the power source is operable to supply the current with a predetermined single polarity claim 1 , the functional unit acting as an anode for said current.5. The device of claim 1 , wherein the functional unit is a Foley catheter claim 1 , a ureteric stent claim 1 , a prostatic stent or a nephrostomy catheter.6. The device of claim 1 , wherein the power source comprises a battery to be placed inside the human or animal body.7. The device of claim 1 , wherein the power source comprises:an energy transmitter to be placed outside the human or animal body, the energy transmitter being operable to transmit energy from outside the body to a location inside the ...

Anchor Systems and Methods

Some embodiments of a medical device anchor system include an anchor device that receives a medical instrument (such as a catheter or the like) and secures the instrument in place relative to a skin penetration point. In some circumstances, the anchor device may allow the anchor device to be used after medical instrument is already in place without the need for a second penetration point for the anchor device. 1. An anchor system for securing a catheter , comprising:a retainer body to releasably couple to an external portion of a catheter when the catheter is occupying a skin penetration point, wherein the retainer body includes a removable cap member releasably attachable with extension elements of the retainer body and being configured to frictionally engage with at least a portion of the outer surface of the catheter when the retainer body releasably couples to the catheter; andfirst and second anchors coupled to the retainer body and being configured to extend distally from a distal end of the retainer body, the first anchor comprising a first subcutaneous flexible tine and the second anchor comprising a second subcutaneous flexible tine, the first and second subcutaneous flexible tines being deployable in a subcutaneous region adjacent to a skin layer to secure the retainer body relative to the skin penetration point,wherein the first and second subcutaneous flexible tines are positioned distal to the distal end of the retainer body when deployable in the subcutaneous region adjacent to the skin layer such that the first and second anchors are configured to deploy into the skin penetration point occupied by the catheter while the retainer body resides fully external to the skin penetration point.2. The anchor system of claim 1 , wherein the retainer body comprises a retention portion comprising a flexible gripping material that defines a channel to receive the external portion of the catheter when the retainer body releasably couples to the catheter.3. The ...

CATHETER CLAMP

A catheter clamp () comprising a base () and a pivotable cover (), the cover arranged to be capable of adopting an open condition and a clamped condition, the clamp further comprising a resiliently biased displaceable latch () to releasably retain the cover in the clamped condition, wherein the latch displaceable on and relative to a support surface () which supports the latch, so as to release the cover from the clamped condition. 1. A catheter clamp comprising a base and a pivotable cover , the cover arranged to be capable of adopting an open condition and a clamped condition , the clamp further comprising a resiliently biased displaceable latch to releasably retain the cover in the clamped condition , wherein the latch is displaceable on and relative to a support surface which supports the latch , so as to release the cover from the clamped condition.2. The catheter clamp of claim 1 , wherein the latch is slidably displaceable.3. The catheter clamp of claim 1 , wherein the latch is displaceably mounted in the base.4. The catheter clamp of claim 1 , wherein the cover comprises a retainer formation arranged to engage with the latch and retain the cover in a clamped condition.5. The catheter clamp of claim 4 , wherein the retainer formation depends from the cover.6. The catheter clamp of claim 4 , wherein the retainer formation is located towards a free end of the cover.7. The catheter clamp of claim 4 , wherein two spaced-apart retainer formations are provided.8. The catheter clamp of claim 4 , wherein the latch is provided with an aperture arranged to receive the retainer formation.9. The catheter clamp of claim 4 , wherein the retainer formation and the latch are provided with respective cam surfaces to facilitate displacement of the latch when urging the cover towards the clamped condition.10. The catheter clamp of claim 9 , wherein the cam surfaces are inclined.11. The catheter clamp of claim 9 , wherein the latch comprises a spring to provide resilient biasing ...

FLEXIBLE WATER VAPOUR BARRIER MULTILAYER TUBE FOR PACKAGING PURPOSE

The application discloses a flexible multilayer tubular package. The package is for an intermittent catheter. The intermittent catheter is coated with a hydrophilic coating, which becomes slippery when in contact with a swelling medium. Thus, the tubular package of the application can with-hold the swelling medium for a long time and at the same time being flexible and bendable. Furthermore, the application discloses a catheter package set, which comprises a multilayer tubular package, an intermittent catheter and a swelling medium. 1. A catheter package:{'sup': '2', 'comprising a multilayer tube sized to receive an intermittent catheter, wherein the tube is formed of tube material that is flexible and has a water vapour transmission rate below 0.50 g/m/mm/24 h.'}2. The catheter package according to claim 1 , wherein the tube material has a water vapour transmission rate below 0.30 g/m/mm/24 h.3. The catheter package according to claim 1 , wherein the multilayer tube comprises at least one thermoplastic polymer layer(s) and at least one thermoplastic elastomer layer(s).4. The catheter package according to claim 1 , wherein the multilayer tube comprises two or more thermoplastic polymer layers.5. The catheter package according to claim 1 , wherein the multilayer tube comprises two or more thermoplastic elastomer layers.6. The catheter package according to claim 3 , wherein the at least one thermoplastic elastomer layer(s) comprises a styrene block copolymer selected from the group consisting of polystyrene-block-poly(ethylene/butylene)-block-polystyrene claim 3 , polystyrene-block-poly(ethylene/propylene)-block-polystyrene claim 3 , polystyrene-block-polybutadiene-block-polystyrene and polystyrene-block-polyisobutylene-block-polystyrene.7. The catheter package according to claim 6 , wherein the thermoplastic elastomer layer(s) further comprises one of polypropylene and polyethylene claim 6 , and a paraffin oil plasticizer.8. The catheter package according to claim 3 ...

ANCHORING SYSTEM FOR A MEDICAL ARTICLE

An anchoring system secures a catheter to the body of a patient and arrests axial movement of the catheter without meaningfully impairing fluid flow through the catheter. The anchoring system includes an anchor pad that adheres to the patient's skin and supports a retainer. The retainer includes interacting structure with a cooperating keeper and latch that releasably moves the retainer between an open and a closed position. When in the open position, the retainer can receive a portion of the catheter and be subsequently moved to the closed position. The retainer further includes one or more retention mechanisms that inhibit axial movement of the catheter relative to the retainer when the catheter is secured therein. In one mode, the retainer includes interacting structure with a keeper and latch. The keeper selectively cooperates with the latch to secure the retainer in a closed position where the cover is generally over to the base. In another mode, the anchoring system includes a mount that allows the retainer to rotate 360° relative to the anchor pad. 1. An anchoring system for securing a medical article having a y-site to a patient , comprising:a base having a groove and a retaining structure, the retaining structure being disposed to lie within the y-site of the medical article and extend in a generally transverse direction; anda cover coupled to the base so as to move between an open position and a closed position, the cover being disposed above the groove in the base to define a channel at least when the cover lies in the closed position, the channel including a proximal end and a distal end and being configured to secure a portion of the medical article, the retaining structure lying outside the distal end of the channel.2. An anchoring system as in claim 1 , wherein the secured portion of the medical article is the y-site.3. An anchoring system as in claim 1 , wherein the groove in the base has a tapering cross-sectional shape.4. An anchoring system as in ...

MEDICAL ARTICLE WITH ROTATABLE WINGS

A medical article is configured to provide access to a patient's vasculature. The medical article includes an elongated body and a pair of stabilizing wings that extend from the elongated body and are configured to stabilize the medical article on a patient. The stabilizing wings are configured to rotate together or independently about the longitudinal axis of the elongated body between at least a first configuration and a second configuration. The elongated body can include a one-way valve disposed therein. The medical article can also one or more adhesive layers configured to releasably attach at least a portion of the wings to a patient. 1. A medical article for use in providing access to a patient's vasculature , the medical article comprising:an elongated body having a longitudinal axis, a distal end, and a proximal end; anda pair of wings extending away from the elongated body, at least one of the pair of wings being configured to rotate about the longitudinal axis of the elongated body between at least a first configuration and a second configuration.2. The medical article of further comprising a catheter extending from the proximal end of the elongated body.3. The medical article of claim 2 , wherein the catheter includes a bevel disposed near a distal end of the catheter claim 2 , the bevel and at least a portion of the rotating wing being rotationally aligned about the longitudinal axis of the elongated body when the wing is in the first configuration.4. The medical article of further comprising a one-way valve disposed within the elongated body.5. The medical article of further comprising an adhesive layer disposed on at least a portion of one side of each of the pair of wings claim 1 , the adhesive layer configured to releasably attach the wings to the patient.6. The medical article of claim 1 , wherein the elongated body comprises a luer connector disposed near the distal end claim 1 , the luer connector being configured to connect the elongated body ...

Catheter Devices and Techniques

This application describes example antimicrobial compositions that may be used alone or in combination with catheters and catheter insertion sites. According to another aspect, the application describes catheters which may employ one or more protection devices, such as cleaning caps, protective caps or both. 1. A catheter assembly comprising a package containing a catheter and at least one cleaning device ,wherein said cleaning device is a cleaning cap, a protective cap or both, andwherein said catheter has at least one port.2. The catheter assembly according to claim 1 , wherein the package is transparent.3. The catheter assembly according to claim 1 , wherein the catheter and each of the at least one cleaning device are individually sealed in separate compartments of the package.4. The catheter assembly according to claim 1 , wherein the catheter is a urinary catheter.5. The catheter assembly according to claim 1 , wherein the package further includes an antimicrobial gel lubricant applied to and/or contained at a tip area of the catheter.6. The catheter assembly according to claim 5 , wherein a portion of the package is fused closely to an exterior of the catheter midway along the length of the catheter to prevent the antimicrobial gel lubricant from migrating away from the tip area and covering another area of the catheter.7. The catheter assembly according to claim 1 , wherein at least a portion of an inside of the catheter contains an antimicrobial composition.8. The catheter assembly according to claim 1 , further comprising an applicator material contained within the at least one cleaning device.9. The catheter assembly according to claim 8 , wherein the applicator material includes an antimicrobial composition.10. A method for using a catheter comprising:providing a catheter assembly, the catheter assembly comprising a package containing a catheter and at least one cleaning device, wherein the catheter has at least one port;opening the package to remove the ...

Assembly For Inserting Foley Catheter

A Foley catheter assembly is disclosed. The Foley catheter assembly includes a Foley catheter, which includes an insertion tip inserted into the bladder and a drainage tube extending from the insertion tip and draining urine from the bladder, and a catheter support cover, which covers the outer surface of the Foley catheter before insertion of the Foley catheter into the bladder to prevent contamination and allows smooth insertion of the insertion tip into the bladder at a constant speed. The catheter support cover includes a pair of support main bodies that are detachably coupled to each other and accommodate the drainage tube and a pair of transport rollers disposed at both sides of the insertion tip at upper portions of the support main bodies to be rotatable for inserting the insertion tip into the bladder. 1. A Foley catheter assembly comprising:a Foley catheter comprising an insertion tip inserted into a bladder and a drainage tube extending from the insertion tip and discharging urine; anda catheter support cover covering the outer surface of the Foley catheter before the Foley catheter is inserted into the bladder for protection from external contamination and assisting the insertion tip to be smoothly inserted into the bladder at a constant speed,wherein the catheter support cover comprises:a pair of support main bodies having an open slit, detachably coupled to each other, and accommodating the drainage tube; anda pair of transport rollers rotatably disposed in upper portions of the support main bodies at both sides of the insertion tip and transporting the insertion tip into the bladder.2. The Foley catheter assembly according to claim 1 , wherein jelly-containing grooves filled with a lubricating jelly are formed to a predetermined depth at upper portions of the pair of support main bodies claim 1 , and the insertion tip and the drainage tube are continuously lubricated with the lubricating jelly at surfaces thereof while passing through the jelly- ...

FLEXIBLE WATER VAPOUR BARRIER TUBE FOR PACKAGING PURPOSE

The application discloses a flexible tubular package. The package is for an intermittent catheter. The intermittent catheter is coated with a hydrophilic coating, which becomes slippery when in contact with a swelling medium. Thus, the tubular package of the application can withhold the swelling medium for a long time and be flexible and bendable at the same time. Furthermore, the application discloses a catheter package set, which comprises a tubular package, an intermittent catheter and a swelling medium. 1. A catheter package formed as a tube for an intermittent catheter , wherein the tube material is flexible and has a low water vapour transmission rate.2. The catheter package according to claim 1 , wherein the tube material has a water vapour transmission rate below 0.50 g/m/mm/24 h.3. The catheter package according to claim 1 , wherein the tube material comprises a thermoplastic polymer.4. The catheter package according to claim 1 , wherein the tube material comprises a thermoplastic elastomer.5. The catheter package according to claim 4 , wherein the thermoplastic elastomer comprises a styrene block copolymer selected from the group consisting of -polystyrene-block-poly(ethylene/butylene)-block-polystyrene claim 4 , polystyrene-block-poly(ethylene/propylene)-block-polystyrene claim 4 , polystyrene-block-polybutadiene-block-polystyrene or and polystyrene-block-polyisobutylene-block-polystyrene.6. The catheter package according to claim 5 , wherein the thermoplastic elastomer further comprises one of polypropylene and polyethylene claim 5 , and paraffin oil plasticizer.7. The catheter package according to claim 1 , wherein the tube material comprises polybutene claim 1 , polyisobutylene claim 1 , cured or uncured butyl rubber claim 1 , or block copolymer with polystyrene as the end blocks such as styrene-isobutylene-styrene.8. The catheter package according to claim 1 , wherein the tube material comprises polyethylene with a density of 0.900-0.920 g/cm.9. The ...

Catheter Set

The present invention relates to a catheter set with a catheter, which has a catheter shaft; a package, which encompasses at least partially the catheter and which has an slide-out removal opening for the catheter; and a gripping aid, which is arranged in the package and which is movable on the catheter shaft, whereby the gripping aid is attached to the package and spaced a distance to the slide-out removal opening in such a manner that package material that can be pushed together is arranged between the gripping aid and the slide-out removal opening. 1. A catheter set comprising: a catheter , which has a catheter shaft; a package , which encompasses at least partially the catheter and which has an slide-out removal opening for the catheter; and a gripping aid , which is arranged in the package and which is movable on the catheter shaft , wherein the gripping aid is attached to the package and spaced a distance to the slide-out removal opening in such a manner that package material that can be pushed together is arranged between the gripping aid and the slide-out removal opening.2. The catheter set according to claim 1 , wherein the gripping aid is formed as a flexible sleeve.3. The catheter set according to claim 1 , wherein the slide-out removal opening is formed in a package end.4. The catheter set according to claim 1 , wherein the slide-out removal opening is formed by a stiffening in the package.5. The catheter set according to claim 1 , wherein a distance between the slide-out removal opening and the gripping aid amounts to at least one-fourth of a length of the catheter shaft.612. The catheter set according to claim 1 , wherein the gripping aid () is fixed in place in the package by at least one sealing seam.7. The catheter set according to claim 1 , wherein a length of the gripping aid amounts to at least 10% of a length of the catheter shaft.8. The catheter set according to claim 1 , wherein an inside diameter of the gripping aid is about 1.5 times to 3 ...

CANNULA RING AND RELATED SYSTEMS AND METHODS

Cannula devices and related methods are provided. In accordance with one embodiment, a cannula ring includes a body portion having a substantially cylindrical member defining an opening therethrough. A plurality of anchor arms coupled with the body portion and configured to be positioned in a first, collapsed state and a second, deployed state, wherein the anchor arms each include a free end that is radially displaced from the body portion while in the second, deployed state relative to their positions while in the first, collapsed state. Suture rings and other associated structures and devices are also described. 1. A cannula ring comprising:a body portion including a substantially cylindrical member defining an opening therethrough;a plurality of anchor arms coupled with the body portion and configured to be positioned in a first, collapsed state and a second, deployed state, wherein the anchor arms each include a free end that is radially displaced from the body portion while in the second, deployed state relative to their positions while in the first, collapsed state.2. The cannula ring of claim 1 , wherein the anchor arms extend substantially axially along the body portion while in the first claim 1 , collapsed state.3. The cannula ring of claim 1 , wherein the anchor arms extend substantially circumferentially about the body portion while in the first claim 1 , collapsed state.4. The cannula ring of claim 1 , wherein the anchor arms are formed of a shape memory material.5. The cannula ring of claim 1 , wherein each anchor arm includes a wire structure.6. The cannula ring of claim 1 , wherein at least a portion of each anchor arm is integrally formed with the body portion.7. The cannula ring of claim 1 , further comprising a coupling structure associated with the body portion.8. The cannula ring of claim 7 , wherein the body portion includes a surface feature configured to engage abutting tissue.9. A cannula device comprising:a first structure having a convex ...

ADHESIVE BACKED IV CATHETER WITH AUTO RELEASE LINER

Intravenous catheter devices are provided which may include one or more adhesive portions which are positioned and configured to temporarily maintain a position of a catheter assembly following catheterization. A release liner covering and protecting the adhesive portions may be automatically removed to reveal the adhesive upon withdrawal of an introducer needle of the catheter assembly. The adhesive may be configured such that a clinician may insert the catheter assembly into the patient, adjust the catheter adapter of the catheter assembly to a desired position, withdraw the introducer needle, thereby removing a protective, non-adhesive release liner from the adhesive of the positioned catheter assembly, thereby temporarily fixing the position of the catheter assembly at the desired position by contacting the exposed adhesive to the skin of the patient. 1. An intravenous catheter assembly , comprising:a catheter adapter;a catheter coupled to an end of the catheter adapter;at least one adhesive portion affixed to the catheter adapter; anda release liner releasably coupled to the at least one adhesive portion.2. The assembly of claim 1 , wherein the catheter adapter further comprises a winged extension claim 1 , and wherein the adhesive portion is affixed to the winged extension.3. The assembly of claim 2 , wherein the at least one adhesive portion is affixed on a bottom side of the winged extension configured to contact the skin of a patient when in use.4. The assembly of claim 3 , wherein at least 50% of the bottom side of the winged extension is covered by the at least one adhesive portion.5. The assembly of claim 2 , further comprising a needle shield claim 2 , wherein a portion of the release liner is permanently attached to the needle shield.6. The assembly of claim 5 , wherein the release liner is folded over.7. The assembly of claim 1 , wherein the adhesive includes an anti-microbial agent.8. A catheter assembly claim 1 , comprising:a catheter adapter having ...

Foldable iv catheter securement dressing for protecting against inadvertent contamination

Sterile intravenous catheter securements and securement dressings that provide simpler, more effective, and lower risk intravenous catheter placement and securement in a patient are described. Catheter securement dressings may include one or more adhesive portions positioned and configured to maintain a position of a catheter assembly following catheterization. Catheter securement dressings may be secured to a patient with an adhesive portion, and the catheter assembly may then be placed into the patient through an access opening in the catheter securement dressing. Portions of catheter securement dressings may then by folded over and adhered to each other and portions of the catheter assembly to secure the catheter assembly to the patient.

MEDICAL DEVICE SECUREMENT SYSTEM

A securement device, system, and method for use with a medical article. The securement device, system, or method may include a body that has a top surface and a bottom surface. The bottom surface has an adhesive compound thereon. A resilient retainer formed from a soft, tacky elastomeric gel or foam is supported by the bottom surface of the body. The resilient retainer receives and secures a medical device. The medical device is secured to the skin of a patient upon affixing the bottom surface to the patient via the adhesive compound. 1. A securement device for a medical device , comprising:a body having a top surface and a bottom surface, said bottom surface having an adhesive compound thereon; anda resilient retainer formed from an elastomeric gel or an elastomeric foam and being supported by said body, said resilient retainer having a channel extending along a longitudinal axis, said channel having a longitudinal axis opening disposed on an underside of the body and being configured to retain at least a portion of a medical device, said medical device being secured to the skin of a patient upon affixing said bottom surface to the patient via said adhesive compound, at least a portion of said resilient retainer being disposed between said body and said medical article along a transverse axis.2. The securement device of claim 1 , wherein said medical device is a catheter.3. The securement device of claim 1 , wherein said channel is preformed into a desired shape for securing the medical device.4. The securement device of claim 3 , wherein said secured portion of said medical device extends entirely through said channel.5. The securement device of claim 1 , wherein said elastomeric gel or said elastomeric foam is formed by curing an organopolysiloxane composition.6. The securement device of claim 5 , wherein said organopolysiloxane composition comprises:a vinyl-containing high viscosity organopolysiloxane or a blend of high viscosity vinyl-containing ...

ANTIFUNGAL CATHETER

A sustained release antimicrobial cannula or catheter for residence within a portion of a human body through which aqueous biological fluids can pass and including a tube. The tube has a polymeric matrix and an antimicrobial agent residing within at least a portion of the polymeric matrix. The polymeric matrix includes cured silicon rubber and the antimicrobial agent is a finely divided nitrofuran compound, a paraben antifungal, or combinations thereof. The antimicrobial agent can diffuse out of the polymeric matrix and into an aqueous biological environment when the polymeric matrix comes into contact with such an aqueous biological environment. Methods of making a sustained release antimicrobial cannula and of catheterizing a patient are also disclosed. 1. A sustained release antimicrobial cannula for residence within a portion of a human body through which aqueous biological fluids can pass , said antimicrobial cannula comprising: a tube having an inner surface , defining an internal lumen , and an outer surface , said tube having a polymeric matrix and an antimicrobial agent residing within at least a portion of the polymeric matrix; wherein the polymeric matrix includes cured silicone rubber; and the antimicrobial agent can diffuse out of the polymeric matrix and into an aqueous biological environment when the polymeric matrix comes into contact with the aqueous biological environment; and wherein at least a finite portion of the polymeric matrix proximate the outer surface includes an amount of from about 10 to about 60% by weight of the antimicrobial agent , and the amount of the antimicrobial agent in the finite portion of the polymeric matrix and the solubility of the antimicrobial agent cooperate to provide a potential for a sustained release diffusion of the antimicrobial agent into the aqueous biological fluids within the human body during normal therapeutic use of the cannula within the human body so long as the aqueous biological fluids are not ...

APPARATUS FOR INTRODUCING PORTALS IN BONE HAVING TRANSVERSELY MOVABLE BONE PROBE

An apparatus for introducing a bone portal into a bone is described herein. An example apparatus for introducing portals into bone includes a stylet and a handle. The stylet is configured to support an infusion tube assembly. The infusion tube assembly comprises a bone portal. The handle is drivingly coupled to the stylet by a release mechanism. The release mechanism comprises a bone probe that, in a first configuration, extends generally parallel to the stylet. The release mechanism is operative to uncouple the driving coupling between the handle and the stylet upon axial motion of the bone probe relative to the handle. The stylet and bone probe are movable apart from one another to a second configuration. 1. Apparatus for introducing a bone portal into a bone , the apparatus comprising:a stylet configured to support an infusion tube assembly comprising a bone portal;a handle drivingly coupled to the stylet by a release mechanism, the release mechanism comprising a bone probe that, in a first configuration, extends generally parallel to the stylet, the release mechanism operative to uncouple the driving coupling between the handle and the stylet upon axial motion of the bone probe relative to the handle;wherein the stylet and bone probe are movable apart from one another from the first configuration to a second configuration, wherein a spacing between the stylet and the bone probe in a direction transverse to the stylet is greater in the second configuration than in the first configuration.2. Apparatus according to comprising an infusion tube assembly removably supported on the stylet claim 1 , the infusion tube assembly comprising a tube having a bone portal at a first end thereof and a fitting at another end thereof claim 1 , the fitting extending transversely outward of the stylet for a distance greater than a spacing between the stylet and the bone probe when the bone probe is in the first configuration.3. Apparatus according to wherein the fitting comprises a ...

DEVICE FOR PROTECTING AND CLEANING THE BLADDER LUMEN

The invention relates to a device (), in particular for protecting and for cleaning the bladder lumen, consisting of at least one functional body () which can be spatially expanded in a variable manner and can be modified at least partially from a small state into a larger state. Said device () protects the bladder lumen from bacterial invasion when the functional body () is inserted into the bladder and helps an infected bladder during mechanical cleaning and subsequent healing. The invention also relates to the use of the device () for medical, in particular prophylactic and therapeutic purposes. 1. Device for protecting and cleaning an urinary bladder lumen , at least comprising:a functional body whose spatial dimensions are variable, wherein the functional body is at least partially transformable from a smaller state to a larger state.2. The device according to claim 1 , wherein the functional body at least partially comprises a material that is permeable to liquids.3. The device according to claim 1 , wherein the material of the functional body is selected from the group consisting of close-meshed tissue claim 1 , porous foil claim 1 , and fine-pored foam.4. The device according to claim 1 , wherein the material of the functional body is a self-inflating material.5. The device according to claim 1 , wherein the functional body is biologically degradable.6. The device according to claim 1 , wherein the functional body is at least partially moistened and/or coated with an antimicrobial substance.7. The device according to claim 1 , wherein the functional body is divided into at least two segments.8. The device according to claim 1 , wherein in the smaller state the functional body is at least partially folded claim 1 , rolled and/or pressed.9. The device according to claim 1 , wherein in the smaller state the functional body has a diameter of at most 4-6 mm.10. The device according to claim 1 , wherein the functional body includes at least two layers.11. The ...

Catheter assembly with resealable opening

A medical device assembly is disclosed, comprising a medical device, preferably having a hydrophilic surface coating, and a package accommodating said medical device. The package if formed of two sheets of foil material, a first foil of which has been deep drawn into a trough shape, the package further comprising a resealable opening arranged within the bounds of the second foil. The medical device may e.g. be a urinary catheter.

Therapeutic agent preparations for delivery into a lumen of the intestinal tract using a swallowable drug delivery device

Embodiments of the invention provide swallowable devices, preparations and methods for delivering drugs and other therapeutic agents within the GI tract. Many embodiments provide a swallowable device for delivering the agents. Particular embodiments provide a swallowable device such as a capsule for delivering drugs into the intestinal wall or other GI lumen. Embodiments also provide various drug preparations that are configured to be contained within the capsule, advanced from the capsule into the intestinal wall and degrade to release the drug into the bloodstream to produce a therapeutic effect. The preparation can be operably coupled to delivery means having a first configuration where the preparation is contained in the capsule and a second configuration where the preparation is advanced out of the capsule into the intestinal wall. Embodiments of the invention are particularly useful for the delivery of drugs which are poorly absorbed, tolerated and/or degraded within the GI tract.

SYSTEMS AND METHODS FOR TREATMENT OF OBESITY AND TYPE 2 DIABETES

The present invention provides systems and methods for treating and controlling obesity and/or type II diabetes. In one aspect of the invention, an internal bypass device includes gastric and duodenal anchors coupled to each other and positioned on either side of the pylorus and a hollow sleeve designed to extend from the pylorus through at least a proximal portion of a patient's small intestine. The gastric and duodenal anchors are movable between collapsed configurations for advancement through the esophagus and an expanded configuration for inhibiting movement of the anchors through the pyloric sphincter. Thus, the bypass device can be placed and removed endoscopically through the patient's esophagus in a minimally invasive outpatient procedure and it is “self-anchoring” and does not require invasive tissue fixation within the patient's GI tract, thereby reducing collateral tissue damage and minimizing its impact on the digestive process. 1. A method for deploying an implant within a target region in a GI tract of a patient comprising:introducing a substantially hollow sleeve through an esophagus and stomach of a patient and into a duodenum;anchoring a proximal portion of the sleeve within a proximal region of the duodenum; anddelivering a fluid into a portion of the sleeve to extend the sleeve through at least a portion of the duodenum.2. The method of wherein the anchoring step comprises inflating an anchor member coupled to the proximal end of the sleeve.3. The method of wherein delivering step is carried out by delivering fluid through an internal lumen extending at least a portion of the length of the sleeve.4. The method of further comprising the step of anchoring a distal end portion of the hollow sleeve within a target region in the intestines.5. The method of wherein the anchoring step is carried out by delivering fluid to a hollow chamber in the distal end portion of the sleeve.6. The method of wherein the introducing step is carried out by coupling the ...

Transparent Catheter Securement System

A securement device for securing a catheter to a patient is provided. The securement device includes a base including a support member and at least one securement arm extending away from the support member. The support member defines a cradle portion, the cradle portion of the support member being configured to receive at least a portion of a catheter. The at least one securement arm being movable over the cradle portion to a position to secure a catheter within the cradle portion. The securement device further includes a cover member configured to be received over the base and dimensioned to secure the base to a patient.

Stretch Valve Balloon Catheter and Methods for Producing and Using Same

A safety catheter includes a flexible, multi-lumen shaft having an outer diameter, a distal tip, a proximal catheter end with a drain end and a proximal inflation end. The multi-lumen shaft defines a drain lumen, a distal hollow balloon portion, at least one inflation lumen, and a drainage port. A hollow stretch valve is coaxially disposed in the inflation or drainage lumen, or both, has a fixed portion within the inflation or drainage lumen, or both, and prevents fluid from passing through the drainage port in a steady state and has a sliding portion slidably disposed within the inflation or drainage lumen, or both, such that, in a stretched state when the proximal catheter end is stretched, the sliding portion slides within the inflation or drainage lumen, or both to permit fluid to pass through the balloon drainage port and/or wall of the catheter. 1. A safety catheter , comprising: a drain lumen extending through the shaft and operable to drain fluid adjacent the distal tip therethrough and out the proximal drain end;', 'a distal hollow balloon portion defining a balloon interior and having at least one inflation port fluidically connected to the balloon interior, the balloon portion operable to be inflated outwardly through the at least one inflation port to a diameter greater than the outer diameter of the shaft;', 'at least one inflation lumen parallel to the drain lumen and fluidically connected to the at least one inflation port, the at least one inflation lumen operable to inflate the balloon interior with an inflation fluid; and', the drain lumen; and', 'the environment of the balloon portion; and, 'a drainage port fluidically connecting at least one of the balloon interior and the at least one inflation lumen to at least one of], 'a flexible, multi-lumen shaft having an outer diameter, a distal tip, a proximal shaft portion, and a proximal catheter end with a proximal drain end and a proximal inflation end, the multi-lumen shaft defining coaxially ...

Context-sensitive flow interrupter and drainage outflow optimization system

Embodiments of the invention provide methods and devices for improved drainage systems and tubing. In one embodiment, a context-sensitive flow interrupter is provided that inhibits or facilitates flow of fluid when engaged with a mating holder. In another embodiment, outflow is optimized through control of the pressure in gas pockets in a tube, drainage tube or assembly. In one such embodiment, gas pockets are vented to inhibit excessive back-pressure or suction on an organ, vessel or cavity being drained. In another such embodiment, loops in the tubes are avoided by using a mechanical template in the form of a groove or peg assembly to thread the slack in the drainage tube to generate a monotonic gradient. In another embodiment, such as for active drainage systems, a bypass channel is provided that allows an applied vacuum to go around an obstruction created by the collection of fluid in an undrained dependent loop.

Endoluminal delivery of anesthesia

Described herein are methods and devices for selectively applying fluids (particularly anesthetics) to a target tissue from within a blood vessel while minimizing the amount of fluid applied to non-target tissue. The injection catheters described herein may include an elongate body, a directional injector, and one or more holdfasts for securing the catheter before extending the injector. The methods of selectively applying anesthetic to a target structure generally include the steps of inserting an injection catheter into a body vessel, positioning the injection catheter within the body vessel near the target structure, anchoring the injection catheter before extending a directional injector from the injection catheter, and applying anesthetic from the injection catheter to the target structure.

CATHETER

The present invention relates to a catheter for realising a volume flow into or out of a human or animal organ, comprising a catheter tube and, at a distance from the distal end of the catheter, an affixing device for mechanically affixing the catheter in the tissue of a human or animal organ. 1. A catheter for realising a volume flow into or out of a human or animal organ , comprising a catheter tube and , at a distance from the distal end of the catheter , an affixing device for mechanically affixing the catheter in the tissue of a human or animal organ.2. The catheter according to claim 1 , wherein the catheter is designed in such a manner that the affixing device abandons its affixing effect when a specific tensile force of 30 N acts on the catheter tube.3. The catheter according to claim 2 , wherein the catheter is designed in such a manner that the affixing device abandons its affixing effect when a specific tensile force of 20 N acts on the catheter tube.4. The catheter according to claim 2 , wherein the affixing device abandons its affixing effect when a tensile force of 10 N acts on the catheter tube.5. The catheter according to claim 1 , wherein the affixing device is arranged at a distance of one-tenth to one-third of the length of the catheter from its distal end.6. The catheter according to claim 1 , wherein the affixing device is embodied by a stent which comprises a hollow cylinder section made of mesh material.7. The catheter according to claim 6 , wherein the stent is designed in such a manner that it expands due to its elasticity when a tensile stress acting in the longitudinal axis of the hollow cylinder is reduced.8. The catheter according to claim 5 , wherein the stent is designed in such a manner that it expands when heat is applied.9. The catheter according to claim 1 , wherein the affixing device is a brace element which claim 1 , in profile claim 1 , is in sections further away from the longitudinal axis of the catheter tube than the outer ...

PREVENTION OF INDWELLING DEVICE RELATED INFECTION: COMPOSITION AND METHODS

Catheters used for medical treatment, e.g., hemodialysis are filled with a locking solution, usually heparin between treatments. To prevent infections, antimicrobial or antibiotic substances have been used as locking solution alone or in combination with antithrombotic substances. It has been found that these locking solutions are rapidly washed out from the catheter tip. The invention describes a thixotropic gel that can be used as locking solution. Beneficial substances, e.g., antimicrobial or antibiotic substances can be added to the gel. A preferred antimicrobial substance is taurolidin alone or in combination with salicylic acid or one of its salts. 110-. (canceled)11. A method for providing microbe-free access to the vascular system of a patient , the method comprising the steps of:providing a catheter;deploying the catheter into the vascular system of a patient; andsealing the catheter with a catheter lock, wherein the catheter lock comprises a thixotropic gel containing an antimicrobial agent therein,12. A method according to wherein the catheter lock is instilled into the catheter using a conventional medical syringe.13. A method according to including the further step of withdrawing the catheter lock from the catheter claim 11 ,14. A method according to wherein the catheter lock is withdrawn from the catheter using a conventional medical syringe.15. A method according to wherein claim 11 , the catheter is a hemodialysis catheter.16. A method according to wherein the thixotropic gel is characterized by:(i) free flow upon the application of a threshold level force imparted by a conventional medical syringe;(ii) sufficient cohesiveness such that, when the composition is moved through the lumen of the catheter using a conventional medical syringe, the composition advances through the lumen as a cohesive rod-shaped mass; and(iii) when the composition is disposed within the lumen of the catheter which is installed in the vascular system of a patient, the ...

Anchoring a Medical Instrument

Some embodiments of a medical anchor device include an elongate body coupled with deployable subcutaneous anchors to secure a catheter instrument (or other medical instrument) in place relative to a skin penetration point. In some circumstances, the elongate body may be in the form of catheter hub body, and the subcutaneous anchors can be deployed from the hub body by adjustment of a movable actuator. A locking member can interact with the actuator so as to retain the actuator in the deployed orientation during the medical procedure. 1. A method for subcutaneously anchoring a catheter instrument , comprising:inserting a distal catheter line of a catheter hub body through a skin penetration point, wherein the catheter hub body provides fluid communication between a first proximal external line connected to the catheter hub body and a first lumen of the distal catheter line and provides fluid communication between the second proximal external line connected to the catheter hub body and a second lumen of the distal catheter line;adjusting a pair of subcutaneous anchor elements from a non-deployed orientation in which the subcutaneous anchor elements are housed inside the catheter hub body to a deployed orientation in which free ends of the subcutaneous anchor elements extend outwardly away from the catheter hub body in a subcutaneous layer proximate to the skin penetration point, wherein the pair of subcutaneous anchor elements are adjusted to the deployed orientation by moving an actuator relative to the catheter hub body; andmoving a locking device to a locked position to releasably maintain the pair of subcutaneous anchor elements in the deployed orientation,wherein the first and second proximal external lines, at least a portion of the actuator, and the locking device remain external to the skin penetration point after the distal catheter line and the pair of subcutaneous anchor elements are inserted through the skin penetration point.2. The method of claim 1 , ...

Low Profile Instrument Immobilizer

This document discusses, among other things, examples of a low profile instrument immobilizer and means for positioning the same. In one example, the low profile instrument immobilizer grasps, secures, and immobilizes an electrode or other instrument that extends through a burr hole in a skull to a target location in a patient's brain. 1. An instrument immobilizer apparatus for immobilizing an instrument relative to a patient , comprising:a base defining a central passage, the base sized and shaped to be disposed about a burr hole of a patient; andan insert received within the central passage, the insert having first and second retaining members, the first and second retaining members movable relative to another and configured for holding therebetween the instrument extending through the central passage into the burr hole.2. The apparatus of claim 1 , wherein the base defines a lateral exit groove sized and shaped to retain a portion of the instrument within the groove.3. The apparatus of claim 1 , wherein the base defines first and second holes on opposite sides of the central passage for fastening the base around the burr hole.4. The apparatus of claim 1 , wherein the insert is coupled to the base with a groove and detent combination to prevent unwanted rotation of the insert relative to the base.5. The apparatus of claim 1 , wherein the insert defines an access opening.6. The apparatus of claim 5 , wherein the first and second retaining members are movable toward and away from one another within the access opening.7. The apparatus of claim 6 , wherein the access opening includes opposing side slide rails slidably carrying the first and second retaining members.8. The apparatus of claim 6 , wherein the first retaining member has a first engagement face and the second retaining member has a second opposed engagement face claim 6 , the first and second engagement faces configured to engage the instrument.9. The apparatus of claim 8 , wherein the first and second ...

SAFETY URINARY CATHETER

There is provided, inter alia, a catheter incorporating one or more of a burstable element, a safety balloon, a marking to indication proper insertion amount for the catheter, a slit valve, and a non-fragmenting retention balloon 1. A catheter comprising:an elongated tubular member comprising a proximal end and a distal end;a fluid inlet disposed at said distal end in fluid communication with a fluid outlet disposed at said proximal end;a first lumen within said elongated tubular member providing fluidic communication between said fluid inlet and said fluid outlet;a retention balloon disposed at said distal end;a retention balloon filling inlet disposed at said proximal end;a second lumen within said elongated tubular member providing fluidic communication between said retention balloon and said retention balloon filling inlet; anda burstable element forming a fluid communication barrier between said second lumen and said first lumen or between said second lumen and space external to said catheter.2. The catheter of claim 1 , further comprisinga safety balloon in fluid communication with said second lumen, said retention balloon filling inlet and said retention balloon, wherein said safety balloon is disposed distal to said retention balloon filling inlet;a marking on said elongated tubular member, said marking disposed at a position indicating proper insertion amount for said catheter; ora slit valve disposed between said first lumen and said second lumen allowing fluid communication between said first lumen and said second lumen upon opening of said slit valve.3. The catheter according to claim 1 , wherein said retention balloon is a non-fragmenting balloon.4. The catheter according to claim 1 , wherein said burstable element bursts at a burstable element bursting pressure claim 1 , and wherein said burstable element bursting pressure is less than a physically harmful inflation pressure.5. The catheter according to claim 4 , wherein said burstable element is not ...

Urethra protection device

It is an object of the present invention to eliminate mechanical stimulation caused by insertion and extraction of such devices as a bladder endoscope and a urethral catheter into and from a urethra. It is a further object of the present invention to make it possible to simultaneously insert such devices as a bladder endoscope and a urethral catheter into the urethra without causing pain. A urethra protection device of the present invention which can be inserted into a urethra includes a first hollow tube in which a bladder endoscope can be inserted, a second hollow tube in which a urethral catheter can be inserted, and a flange provided on an outer peripheral part of the urethra protection device at a position separated from a forward end thereof which is first inserted into the urethra.

INTRAVENOUS THERAPY

A medical device is disclosed that can be used to provide a space at an IV catheter site so that kinking of the IV is substantially prevented. The disclosed medical device includes a spacer and an attachment material. The attachment material maybe an elongated strap. The spacer may comprise an elongated member. The elongated strap may be elastomeric and self-adhesive. 1. A medical device for enabling the consistent flow of fluids when an intravenous catheter is placed in an antecubital vein , the medical device comprising:a spacer having a first end and a second end, the spacer comprising a pliable member configured to be positioned near the flexor region of a patient's arm; andan elongated strap connected to the spacer, the strap having a member-enclosing portion configured to hold the member in position substantially over the intravenous catheter site such that the patient is able to flex upper extremities without kinking the intravenous catheter;wherein the elongated strap is elastomeric and self-adhesive.2. The medical device of claim 1 , wherein the member has a first end claim 1 , a second end claim 1 , and a central portion and the first and second ends are tapered.3. The medical device of claim 1 , wherein the elongated strap is elastomeric in only one direction.4. The medical device of claim 1 , wherein the elongated strap comprises a slit.5. The medical device of claim 1 , wherein the elongated strap has a two trapezoidal tabs that are configured to wrap around the member and secure the member in place on the elongated strap.6. A medical device for enabling the consistent flow of fluids when an intravenous catheter is placed in an antecubital vein claim 1 , the medical device comprising:a spacer having a first end and a second end, the spacer comprising a pliable member configured to be positioned near the intravenous catheter site; andan elongated strap connected to the spacer, the strap being configured to hold the member in position substantially over ...

METHOD FOR APPLYING ANTIMICROBIAL TO PROXIMAL END OF CATHETER

Systems, methods, and articles for delivering an antimicrobial composition to the proximal elements of a trans-dermal catheter and into the lumen of the transdermal catheter are disclosed. In an embodiment, an antimicrobial composition placed on an interior surface a cap element, and transfers antimicrobial to the exterior of the proximal end of the transdermal catheter. The system comprises an elongate member configured for insertion into a lumen of a catheter, the elongate member containing an antimicrobial. 1. A method of delivering an antimicrobial composition to the proximal end of a transdermal catheter , the method comprising: i) a hub located at the proximal end of the catheter,', 'ii) exterior threads on the proximal end of the hub, and', 'iii) an interior channel in the hub leading from an opening at the proximal end of the catheter to a lumen in the catheter, wherein at least a portion of the interior channel has a tapered interior surface;, 'a) providing a transdermal catheter implanted within a patient, the transdermal catheter having a proximal end located outside of the patient and a distal end located at least partially within a blood vessel of the patient, the catheter comprising i) a retaining ring comprising threads configured to engage the exterior threads on the catheter hub;', 'ii) a soluble non-liquid antimicrobial composition located on the threads of the retaining ring; and', 'iii) a tapered member configured for insertion into the catheter hub, the tapered member configured to substantially seal the proximal end of the catheter;, 'b) providing an antimicrobial composition delivery device for insertion into the proximal opening of the catheter, the antimicrobial composition delivery device comprisingc) injecting a liquid lock solution into the transdermal catheter such that at least the proximal end of the transdermal catheter is substantially filled with the lock solution; andd) insertion of the tapered member of the antimicrobial delivery ...

EXPANDABLE INTRODUCER SHEATH TO PRESERVE GUIDEWIRE ACCESS

An introducer sheath is described. The introducer sheath may include a tubular body. The tubular body may extend from a distal end toward a proximal end. The tubular body may include a lumen. The lumen may at least partially be defined by a wall. A channel may be disposed within the wall. The channel may be configured to receive a guidewire. The tubular body may include an expandable portion expandable to increase a cross-sectional area of the lumen. 1. An introducer sheath comprising: a lumen defined at least partially by a wall;', 'a secondary channel being disposed within the wall and configured to receive a guidewire., 'a tubular body extending from a distal end toward a proximal end, the tubular body comprising2. The introducer sheath of claim 1 , the tubular body further comprising at least one deformable expandable portion configured to increase a cross-sectional area of the tubular body.3. The introducer sheath of claim 2 , wherein at least one deformable expandable portion is located between the lumen and the secondary channel.4. The introducer sheath of claim 3 , wherein the deformable expandable portion splits when the deformable expandable portion expands beyond a predetermined diameter and/or a predetermined expansion distance.5. The introducer sheath of claim 2 , wherein a portion of the tubular body splits when expanded beyond a predetermined diameter and/or a predetermined expansion distance.6. The introducer sheath of claim 3 , wherein the tubular body further comprises a geometric pattern formed on at least a portion of an inner wall of the tubular body to facilitate splitting a portion of the tubular body.7. The introducer sheath of claim 6 , wherein the geometric pattern comprises at least one of:a groove that facilitates splitting of at least a portion of the tubular body;a groove that facilitates splitting of at least the deformable expandable portion;a separation line to facilitate splitting of at least a portion of the tubular body;a ...

BLOOD ACCESS DEVICE

A blood access device including a fluid conduit configured to convey a flow of fluid to a target vessel, a second lever element pivotally and resiliently connected to a first lever element such that it may move from a first position to a second position. A biasing force is exerted on the second lever element for moving it from the first position to the second position, and a blocking member may be activated by the second lever element, such that a flow of fluid is decreased when the second lever element is moved from the first position to the second position. The lever elements are configured to be fixed to the target vessel when the second lever element is in the first position, and the second lever element moves to the second position and activates the blocking member if the fixation is at least partially lost. 1. A blood access device comprising:a fluid conduit configured to convey a flow of fluid to a target vessel,a first lever element,a second lever element pivotally and resiliently connected to the first lever element such that the second lever element is movable in a direction from a first position to a second position in relation to the first lever element, and a biasing force is exerted on the second lever element for moving the lever element from the first position to the second position,a blocking member configured to be activated by the second lever element, such that a flow of fluid conveyed by the fluid conduit is decreased when the second lever element is moved from the first position to the second position, whereinthe first and second lever elements are configured to be fixed at a surface of the target vessel when the second lever element is in the first position, such that the fixation to the surface counteracts the biasing force exerted on the second lever element, thereby allowing the second lever element to move to the second position and activate the blocking member if the fixation is at least partially lost.2. A blood access device according ...

PROTECTIVE DEVICE FOR PROTECTING A PORT NEEDLE OR HUBER NEEDLE

Protective device for protecting a port needle or Huber needle against shifting and for protecting at least one port needle puncture site and/or incision site. A frame-like spacer element is provided with an inner opening, recess or cutout for surrounding or receiving the port needle or Huber needle, which frame-like spacer element has a height corresponding to at least half the height of the port needle or Huber needle and has at least one means for fixing or securing the spacer element in the area of a port. 118-. (canceled)19. A Protective device for protecting a port needle or Huber needle against shifting and for protecting at least one port needle puncture site and/or incision site , wherein a frame-like spacer element is provided with an inner opening , recess or cutout for surrounding or receiving the port needle or Huber needle , which frame-like spacer element has a height corresponding to at least half the height of the port needle or Huber needle and has at least one means for fixing or securing the spacer element in the area of a port , and wherein the spacer element is in one part.20. The Protective device according to claim 19 , wherein at least one cover means claim 19 , in particular a cover film claim 19 , is provided for sealingly covering the frame-like spacer element.21. The Protective device according to claim 20 , wherein the cover means is formed integrally with the frame-like spacer element or is firmly connected thereto.22. The Protective device according to claim 19 , wherein the spacer element is made of a material that takes up or absorbs liquid.23. The Protective device according to claim 19 , wherein the spacer element is gel-like claim 19 , in particular made of a glycerol gel material.24. The Protective device according to claim 19 , wherein the frame-like spacer element is profiled and/or has incisions or folding aids claim 19 , particularly in one or more corner areas.25. The Protective device according to claim 19 , wherein the ...

TIME-SENSITIVE CATHETER ALARM

A catheter includes an elongated tube, wherein a portion of the elongated tube is positionable inside the body of a subject such that, during use, bodily fluids travel from the subject through the elongated tube. A timing device is coupled to the elongated tube, wherein, after the catheter is inserted into the body of the subject, the timing device provides an indication of the amount of time that the catheter has been disposed inside the subject. 1. A catheter system comprising:an elongated tube, wherein a portion of the elongated tube is positionable inside the body of a subject such that, during use, bodily fluids travel from the subject through the elongated tube;a collection container coupled to the elongated tube, wherein bodily fluids from the subject are collected in the collection device; anda timing device coupled to a portion of the catheter system, wherein, after the catheter is inserted into the body of the subject, the timing device provides an indication of the amount of time the catheter has been disposed inside the subject.2. The catheter system of claim 1 , wherein the elongated tube comprises a distal end and a proximal end claim 1 , the distal end being positionable inside the body of a subject during use claim 1 , and the proximal end being coupleable to a collection container such that claim 1 , during use claim 1 , the bodily fluids travel through elongated tube to the collection container.3. The catheter system of claim 1 , wherein the catheter is a catheter for draining urine from the bladder of the subject.4. The catheter of system claim 1 , wherein the timing device is a light that provides a visual signal that indicates the amount of time that the catheter has been disposed inside the subject.5. The catheter of system claim 4 , wherein the light is an LED light claim 4 , and wherein the LED light produces pulses of light claim 4 , the frequency of the pulses of light providing a visual indication of the amount of time that the catheter ...

Male Telescope Catheter

A catheter includes a proximal section that is inserted into and telescopically movable relative to a distal section. A proximal end of the proximal section is insertable into a urethra of a user and the distal section provides a discharge conduit for urine. The proximal section includes a rear portion, and an exterior surface of the rear portion diverges away from the proximal end to provide a diverging rear transition section that is wider than the proximal end of the proximal section. The distal section includes a front portion and an interior surface of the front portion converges to an opening formed in a front transition end, the opening is narrower than the diverging rear transition section of the proximal section. 1. A catheter comprising:a proximal section that is inserted into and telescopically movable relative to a distal section, a proximal end of the proximal section is insertable into a urethra of a user and the distal section provides a discharge conduit for urine;wherein the proximal section includes a rear portion, and an exterior surface of the rear portion diverges away from the proximal end to provide a diverging rear transition section that is wider than the proximal end of the proximal section;wherein the distal section includes a front portion and an interior surface of the front portion converges to an opening formed in a front transition end, the opening is narrower than the diverging rear transition section of the proximal section.2. The catheter of claim 1 , wherein the proximal section includes a bump formed in a radial direction that is located between the diverging rear transition section and the proximal end claim 1 , and the opening is narrower than the bump.3. The catheter of claim 2 , wherein the proximal section is inserted into the distal section in a collapsed configuration that locates the bump distal the opening claim 2 , and the proximal section is movable to an expanded configuration that locates the bump proximal of the ...

Pulmonary nodule access devices and methods of using the same

In certain embodiments, a device is configured to be delivered to the site of a nodule in the lung or other body organ or lumen. The device can be configured to attach directly to the target nodule or to tissue adjacent the target nodule. The device can be configured to provide repeatable access to the site of the target nodule. In some embodiments, the device includes a guide wire that can extend proximal the device. The guide wire can be configured to engage with a catheter or other medical device to provided repeatable and dependable navigation to the site of the target nodule. In some embodiments, the device can include a channel portion through which medical devices and/or instruments can be navigated. In some embodiments, the device can be deployed in the wall of an airway or other body lumen to provide transluminal access to a nodule outside of the lumen.

Indwelling Urinary Catheterization Assembly

An indwelling urinary catheter assembly is disclosed having an indwelling catheter and a sheath enclosing an insertable portion of the indwelling catheter. 1. An indwelling urinary catheter assembly comprising:an indwelling catheter comprising a first end having a urine inlet, a second end having a urine outlet, a takeoff port having a port bore, an expander, and a urethra insertable portion, wherein the urine inlet and urine outlet are in fluid communication with one another and wherein the port bore and the expander are in fluid communication with one another;a pliable sheath comprising a lumen, wherein the sheath encloses at least a portion of the insertable portion; andan introducer attached to the sheath, wherein the introducer is dimensioned and configured to enclose and support the first end when in an initial position, the introducer slidingly receives the insertable portion during insertion of the insertable portion into the urethra of a patient, wherein the introducer is dimensioned and configured to be partially inserted into the urethra of a patient, and the introducer together with the sheath encloses all of the urethra-insertable portion when in the initial position;wherein the sheath further comprises a first terminus having a first collar, the first collar being fixed to the introducer, and a second terminus directly coupled to an area of the catheter that includes a portion of the takeoff port;and wherein the second terminus comprises a second collar having at least one vent in fluid communication with the lumen and an environment outside the sheath, the vent being dimensioned and configured to relieve a pressure build-up within the sheath.2. The indwelling catheter assembly of claim 1 , wherein the second terminus sealingly engages the catheter at an attachment point at the area including the portion of the takeoff port.3. The indwelling catheter assembly of claim 1 , further comprising a non-insertable portion claim 1 , wherein at least part of ...

ASSEMBLY WITH A GUIDE WIRE AND A FIXATOR FOR ATTACHING TO A BLOOD VESSEL

A fixator assembly comprising a fixator for fixing inside a blood vessel, the fixator being able to slide proximally along a guide wire. The assembly comprising means for preventing the fixator from moving distally of the preventing means. A tubular element for introduction into a blood vessel of a person, the tubular element comprising an end opening and a plurality of side openings as well as a transport wire extending from inside the tubular element and to the surroundings thereof through an individual side opening. 19.-. (canceled)10. An assembly of:a guide wire having a distal end for introduction into a blood vessel and a proximal end,a fixator for releasably attaching to an inner side of the blood vessel andmeans preventing the fixator from travelling distally beyond the preventing means, wherein:the fixator is adapted to move toward the proximal end of the guide wire independently of the guide wire andthe fixator is adapted to maintain attachment to the inner side of the blood vessel, when a pulling force of at least 0.1N is applied to the guide wire and, via the preventing means, to the fixator.11. The assembly according to claim 10 , wherein the fixator has:a deformable portion having a central portion adapted to attach to the inner side of the blood vessel at a predetermined length thereof, along a first longitudinal direction of the blood vessel,a distal part attached to the deformable portion,a proximal part attached to the deformable portion,wherein the deformable portion is adapted to exert at least substantially the same force to the blood vessel along all of the predetermined length when the pulling force of at least 0.1N is exerted to the guide wire and fixator.12. The assembly according claim 10 , wherein the fixator has:a deformable portion having a central portion adapted to attach to the inner side of the blood vessel,a distal part attached to the deformable portion,a proximal part attached to the deformable portion and being translatable, ...

NON-INVASIVE URINE DIRECTIONAL DEVICE, URINE COLLECTION SYSTEM, AND KIT

A non-invasive urine directional device, urine collection system, and kit are provided for a physically active user. The urine directional device includes a form-fitting undergarment or a band fastened to an open top, non-invasive receiving body in fluid communication with a drainage element. The urine collection system includes a urine directional device and a urine disposal assembly having urine collection bags. The kit includes a reusable urine directional device and a reusable wash bag. 1. A urine directional device including:(a) a form-fitting undergarment having a pant shape with a first defined leg portion, a second defined leg portion, and an open crotch portion, the first defined leg portion and the second defined leg portion configured to extend to at least an upper region of a user's thighs;(b) a receiving body configured to be non-invasive and to receive and direct a urine flow away from a user's body, the receiving body having an open-top proximal end that tapers to a distal end, the proximal end fastened to the open crotch portion of the form-fitting undergarment around a circumference of the open crotch portion; and(c) a drainage element in fluid communication with the receiving body and configured to extend a urine flow away from a user's body, the drainage element fastened to the distal end of the receiving body.2. The device according to wherein said form-fitting undergarment is made from a shaper material.3. The device according to wherein said form-fitting undergarment is constructed from a material comprising 10% spandex and 90% nylon.4. The device according to wherein the form-fitting undergarment is a 360-degree stretch material.5. The device according to wherein the receiving body is constructed from a material selected from the group consisting of a silicone based material claim 4 , a polyurethane claim 4 , or a combination thereof.6. The device according to wherein drainage element constructed from a material selected from the group ...

Stretch Valve Balloon Catheter and Methods for Producing and Using Same

A safety catheter includes a flexible, multi-lumen shaft having an outer diameter, a distal tip, a proximal catheter end with a drain end and a proximal inflation end. The multi-lumen shaft defines a drain lumen, a distal hollow balloon portion, at least one inflation lumen, and a drainage port. A hollow stretch valve is coaxially disposed in the drainage lumen and has a radially self-expandable proximal section fixedly connected within the drain lumen by self-expansion, a flexible intermediate section longitudinally movable within the drain lumen, and a distal plug movably positioned in the drain lumen to prevent fluid from passing through the drainage port in a steady state and being slidably disposed within the drain lumen such that, in a stretched state when the proximal catheter end is stretched, the distal plug slides within the drain lumen to permit the inflation fluid to pass through the drainage port. 1. A safety catheter , comprising: a drain lumen extending through the shaft and operable to drain fluid adjacent the distal tip therethrough and out the proximal drain end;', 'a distal hollow balloon portion defining a balloon interior and having at least one inflation port fluidically connected to the balloon interior, the balloon portion operable to be inflated outwardly through the at least one inflation port to a diameter greater than the outer diameter of the shaft;', 'at least one inflation lumen parallel to the drain lumen and fluidically connected to the at least one inflation port, the at least one inflation lumen operable to inflate the balloon interior with an inflation fluid; and', 'a drainage port fluidically connecting at least one of the balloon interior and the at least one inflation lumen to the drain lumen; and, 'a flexible, multi-lumen shaft having an outer diameter, a distal tip, a proximal shaft portion, and a proximal catheter end with a proximal drain end and a proximal inflation end, the multi-lumen shaft defining a radially self- ...

URINARY CATHETER ANTI-REFLUX AND PATHOGEN BLOCK DEVICE

The present disclosure generally pertains to a device and system for preventing urinary backflow into the urinary tract of a patient. The device comprises a one-way valve which allows for unobstructed urine flow in the direction of the urine towards the urine collection container and away from the catheter. The device prevents backflow into the catheter in situations where the urine collection container is raised above the level of the bladder. The components on the exit side of the valve are coated with an antimicrobial substance to prevent bacterial contamination of the system. The exit volume also contains a silver coated high surface area element to serve as an antibacterial kill site. The inlet side of the device has a volume and access port for urine sampling, with a one-way valve element providing isolation from contamination from the urine collection system. 1. A catheter reflux prevention device , comprisinga tubular member having an inlet for receiving urine from tubing connecting the tubular member to a catheter, the tubular member having an outlet for permitting the urine to egress from the tubular member, the tubular member defining an inlet chamber and an outlet chamber; anda one-way valve defining the boundary between the inlet chamber and the outlet chamber.2. The device of claim 1 , further comprising a cartridge positioned within the outlet chamber and defining a passage for the urine claim 1 , wherein a surface of the cylindrical cartridge defining the passage is coated with at least one layer of an antimicrobial substance.3. The device of claim 2 , wherein the antimicrobial substance comprises silver.4. The device of claim 2 , wherein an interior surface of the outlet chamber is coated with at least one layer of an antimicrobial substance.5. The device of claim 1 , further comprising a sample valve having an opening through which samples may be drawn from the inlet chamber.6. The device of claim 1 , further comprising a needless sample valve ...

Variable Stiffness Catheter, Intraluminal Treatment System, And Method

A variable stiffness catheter includes an elongate tubular body having proximal and distal body ends and defining a lumen extending longitudinally between a fluid inlet in the proximal body end and a fluid outlet in the distal body end. The catheter includes a vacuum responsive stiffener coupled with the elongate tubular body, which may include a stiffening medium such as an open cell foam having an expanded state and a vacuum collapsed state. The stiffening medium can transition between the expanded state at which it is relatively flexible and the vacuum collapsed state at which it is relatively inflexible via withdrawing fluid from the vacuum responsive stiffener by way of a vacuum device.

Medical Lanyard

A medical lanyard for securing a feeding tube to a patient, increasing patient maneuverability, and protecting against unintended removal of the feeding tube is provided. The medical lanyards are worn around a patient's neck or clipped to the patient's clothing. The medical lanyard securely suspends a feeding tube port connector and the corresponding feeding tube while providing for easy disconnect of the feeding tube port connector/feeding tube combination from either the necklace or the clip, or from the nutrient supply. The medical lanyards also provide for protection of the feeding tube stomach insertion point so that it is not compromised when tension is applied between the feeding tube port connector/feeding tube combination and either the remainder of the medical lanyard or the nutrient supply.

MODIFIED FLOW CATHETERS AND METHODS OF USE THEREOF

A catheter includes an elongate body defining a continuous enclosed liquid flow channel, at least a portion of the liquid flow channel including a modification having a first surface and a second surface and an included volume between the first surface and the second surface, at least a portion of the included volume defining an elongated air flow channel, at least a portion of the first surface and the second surface coated with a hydrophobic (e.g., superhydrophobic) material. The catheter can be a urinary catheter (e.g., a urine drainage tube connected to a urine collection bag). Methods of flowing liquid through a catheter and of catheterizing a patient are encompassed. 1. A catheter comprising an elongate body defining a continuous enclosed liquid flow channel , at least a portion of the liquid flow channel comprising a modification having a first surface and a second surface and an included volume between the first surface and the second surface , at least a portion of the included volume defining an elongated air flow channel , at least a portion of the first surface and the second surface coated with a hydrophobic material , whereby the air flow channel excludes liquid flow but is in fluid communication with the liquid flow channel.2. The catheter of claim 1 , wherein at least one of the modification and the hydrophobic material have anti-microbial properties.3. The catheter of claim 1 , wherein the hydrophobic material is superhydrophobic.4. The catheter of claim 1 , wherein the continuous enclosed liquid flow channel extends for the length of the elongate body.5. The catheter of claim 1 , wherein the air flow channel is contiguous with the continuous liquid flow channel.6. The catheter of claim 1 , wherein the elongate body defines an inner wall and an elongated rod is disposed within the continuous liquid flow channel and is attached to the inner wall claim 1 , the rod being coated at least in part with the hydrophobic material.7. The catheter of claim 1 , ...

Catheter Assembly

A urinary catheter assembly () is provided. The catheter assembly has an intermittent urinary catheter () with low-friction surface and a tubular elongated package () with a side-opening (). The catheter may be provided with a hydrophilic surface and the package may include a liquid swelling medium. The user may grab the connector () through the side-opening and pull out the catheter of the package through there. Spillage of the liquid swelling medium or lubricant is avoided. The side-opening may be configured so that it has two stable configurations, a storing and a folded configuration. 1. An intermittent urinary catheter assembly comprising:an intermittent urinary catheter comprising a catheter tube having a proximal end and a distal end, where the proximal end comprises a catheter tip and the distal end comprises a catheter connector, anda catheter package for accommodating the intermittent urinary catheter, wherein the package is of a general elongate shape having a proximal end and a distal end and is made of a tubular material, where the package comprises a cavity for accommodating at least the insertable part of the catheter tubewherein the catheter package is provided with an opening arranged in a predefined area in a side wall of the tubular material for allowing extraction of the catheter from the package.2. The intermittent urinary catheter assembly according to claim 1 , wherein the intermittent urinary catheter is provided with a hydrophilic surface coating.3. The intermittent urinary catheter assembly according to claim 1 , wherein the tubular material has side walls made of gas impermeable material.4. The intermittent urinary catheter assembly according to claim 1 , wherein the opening in the predefined area is a through-going opening.5. The intermittent urinary catheter assembly according to claim 1 , wherein the opening in the predefined area is a weakening line along the periphery of the predefined area.6. The intermittent urinary catheter ...

Catheter assembly with resealable opening

A catheter assembly includes a catheter, preferably having a hydrophilic surface coating; and a package accommodating said catheter. The package preferably also accommodates a wetting fluid. The package includes a first and a second sheet material connected around the edges; a perforation line extending along a non-closed loop in one of said sheet materials, which defines a flap opening; a third sheet material connected by means of an adhesive over said flap opening. The third sheet material with a margin covers the entire flap opening. The adhesive is adapted to maintain a sterile closure of the package before use, and to be resealable after use. The third sheet material forms a tab not provided with adhesive and the tab provides a grip portion for peel opening of the package.

MEDICAL DEVICE FOR APPLYING ANTIMICROBIAL TO PROXIMAL END OF CATHETER

Systems, methods, and articles for providing an antimicrobial composition to the proximal elements of a trans-dermal catheter and into the lumen of the transdermal catheter are disclosed. In an embodiment, an antimicrobial composition on surface a cap element transfers antimicrobial to the proximal end of the transdermal catheter. The system comprises an elongate member configured for insertion into a lumen of a catheter, the elongate member containing an antimicrobial. 1. A device for insertion into the hub of a transdermal catheter to provide antimicrobial properties , the device comprising: i) an outer surface for handling the device, and', 'ii) an inner volume having an interior surface, the interior surface containing threads configured to engage the threads on the transdermal catheter;, 'a) a cap configured to be removably secured to the proximal end of a transdermal catheter, the cap comprisingb) a tapered member positioned at least partially within the inner volume of the cap, such that the tapered member is located opposite the threads of the cap; andc) an elongate member secured to the tapered member and configured for insertion into the hub of the transdermal catheter, the elongate member comprising an antimicrobial agent;wherein the tapered member and elongate member are configured for insertion into the proximal end of the transdermal catheter such that antimicrobial agent from the elongate member is delivered into the hub of the transdermal catheter.2. The device of claim 1 , wherein the elongate member is less than 25 millimeters long.3. The device of claim 1 , wherein the elongate member is less than 2.5 millimeters wide.4. The device of claim 1 , wherein the elongate member is substantially rigid.5. The device of claim 1 , wherein the elongate member is sufficiently self-supporting to maintain its shape under its own weight.6. The device of claim 1 , wherein the tapered member has a taper of at least 5 percent.7. The device of claim 1 , wherein the ...

Three-Lobe Drainage Hose

A drainage system includes a drainage tube, a tubular coupling, and a drainage hose. The drainage tube defines an inner passage and terminating in a first drainage end and a second drainage end. The tubular coupling has a first thickness that runs throughout the coupling and forms a passage and a stop determined by a second thickness. The drainage hose is formed by a profile which runs along a length of the drainage hose and terminates in a first drainage end and a second drainage end.

Catheter device

A catheter assembly comprising an elongated tubular structure having a distal end and a proximal end; a septum disposed within the interior of the tubular structure so as to define a first lumen and a second lumen, and a valve element disposed at the distal end of the tubular structure and configured to move longitudinally relative to the tubular structure between (i) a closed position in which the distal end of the tubular structure is closed off by the valve element, and (ii) an open position in which the distal end of the tubular structure is not closed off by the valve element; wherein the tubular structure, septum and valve element are configured so as to provide fluid communication between the first and second lumen when the valve element is disposed in its closed position.

DRESSING HAVING INTEGRAL ANTIMICROBIAL

A dressing having integral antimicrobial includes a transparent film layer having a top side, an opposite bottom side, and an insertion site viewing portion. The dressing also includes an antimicrobial member having a top side and an opposite bottom side. The antimicrobial member top side is adhered to the film layer bottom side in the insertion site viewing portion. The antimicrobial member includes at least one pair of elongated, spacedly disposed portions defining a slot therebetween. A zone of inhibition defined by the antimicrobial member covers an entire area of the slot between the member portions. 127-. (canceled)28. A dressing comprising:a transparent film layer having a top side, an opposite bottom side, and an insertion site viewing portion; andan antimicrobial member having a top side and an opposite bottom side, said antimicrobial member top side being adhered to said transparent film layer bottom side in said insertion site viewing portion;said antimicrobial member including at least one pair of elongated, spacedly disposed portions defining a slot therebetween, the slot having a width sized to accept a catheter lumen;wherein a zone of inhibition defined by said antimicrobial member entirely covers the slot; andwherein the transparent film layer bottom side includes an adhesive position and an adhesive-free portion, the adhesive-free portion being disposed in the slot between the antimicrobial member portions.29. The dressing of claim 28 , wherein said antimicrobial member bottom side includes an adhesive thereon.30. The dressing of claim 29 , wherein said antimicrobial member bottom side includes an adhesive free portion adjacent said slot.31. The dressing of claim 28 , wherein said antimicrobial member bottom side has no adhesive thereon.32. The dressing of claim 28 , wherein said slot has a width approximately in the range of 0.05 inches to 0.4 inches.33. The dressing of claim 28 , wherein said antimicrobial member includes at least one of an ...

Vacuum anchoring catheter

Provided is a method for the treatment of blood vessel occlusions, comprising the localized anchoring of a catheter during the procedure by temporarily adhering its tip to the occlusion treatment site using a vacuum. Also provided is a catheter with a vacuum anchoring tip controlled by an externally generated vacuum, a catheter with a vacuum anchoring tip controlled by a self-generated vacuum, and a catheter with a vacuum anchoring tip in which the vacuum is controlled by an electronic signal. The localized anchoring method utilizes a vacuum to secure the tip of the catheter in place while allowing a free passage for the wire or dedicated occlusion penetrating device, and thereby frees the operator from constantly monitoring the tip position and pushing the catheter to support the advancement of the wire.

SAFE NEEDLE METHODS, APPARATUS, AND SYSTEMS

A bandage can be used to secure a needle to an access site so as to prevent unintended movement or withdrawal of the needle from the access site during administration of a treatment to a patient. After treatment, the needle can be removed by manipulating a portion of the bandage. Another portion of the bandage can be maintained in position over the access site during needle removal and can be used to promote clotting of the site after needle removal. The bandage may include a clotting agent, a hemostasis pad, and/or a clot-promoting structure. Additionally or alternatively, finger pressure can be applied to the access site through the bandage. For example, the bandage may include a viewing window without any adhesive to allow visual monitoring of the access site during treatment. Finger pressure may be applied to the viewing window and thereby to the access site during and after needle removal to encourage hemostasis. 121-. (canceled)22. A bandage for securing a butterfly needle to a patient access site , the needle having a pair of wings extending radially from the hub of the needle , the bandage comprising: a first region with a first adhesive on at least a surface portion thereof, a window in said first region being transparent and without any adhesive thereon;', 'a second region with a gap therein so as to form a pair of tabs separated by said gap, at least an end portion of each of the tabs being free from adhesive; and', 'a third region arranged between the first and second regions, the third region having a second adhesive on at least a surface portion thereof;, 'a flexible material havingwherein the third region is arranged so as to contact the pair of wings of the butterfly needle for releasably coupling the bandage thereto, andthe window is arranged so as to be located over the patient access site when the third region is coupled to the butterfly needle inserted into said access site.2333-. (canceled)34. A bandage comprising a flexible material including:a ...

BALLOON CATHETER

A balloon catheter having an elongated catheter shaft defining a fluid drainage lumen and a balloon inflation lumen. The balloon catheter includes a fluid drainage port disposed about the distal end of the catheter shaft in fluid communication with the fluid drainage lumen, and a balloon inflation port disposed about the distal end of the catheter shaft in fluid communication with the balloon inflation lumen. A balloon portion is disposed about the distal end of the catheter shaft in fluid communication with the balloon inflation port. A release device is disposed in fluid communication with the balloon portion and the fluid drainage lumen, and includes an activating member. A tether is attached to the activating member of the release device. Tension applied to the tether activates the release device, enabling fluid flow from the balloon portion into the fluid drainage lumen and out of the body. 116-. (canceled)17. A method of balloon catheterization comprising activating a release device using a tether to deflate a balloon catheter.18. The method of claim 17 , wherein the balloon catheter is positioned inside a body and wherein activating a release device using a tether to deflate a balloon catheter comprises applying a tension force to the tether from outside the body.19. The method of claim 17 , wherein activating a release device using a tether to deflate a balloon catheter comprises opening a port between a balloon inflation lumen and a fluid drainage lumen using the release device.20. The method of claim 19 , wherein activating a release device using a tether to deflate a balloon catheter comprises channeling balloon inflation fluid from the balloon inflation lumen to the fluid drainage lumen through the port.21. The method of claim 17 , wherein activating a release device using a tether to deflate a balloon catheter comprises inserting a balloon catheter including a fluid drainage lumen claim 17 , a balloon inflation lumen claim 17 , and a balloon into a body ...

MEDICAL CONDUIT PROTECTION DEVICES, SYSTEMS AND METHODS

A medical conduit protection device has, for example, an elongate body having a wall defining a lumen for one or more elongate medical conduits. The device also includes first and second tethers provided on opposed ends of the body for securing the device to a point on or near a patient, and an external point. The medical conduit protection device inhibits tampering with or damage to the one or more medical conduits within the lumen of the body by shielding, gathering, transferring externally-applied strain away from, or otherwise protecting the one or more medical conduits within the lumen thereof. 1. A medical conduit protection device comprising:a.) an elongate body having a wall, defining a lumen therein, and having first and second opposed ends, the body being adapted and configured to receive, within the lumen thereof, one or more elongate medical conduits;b.) a first tether provided on the first end of the body, the first tether being adapted and configured to secure the first end of the body to a patient-end anchor point; andc.) a second tether provided on the second end of the body, the second tether being adapted and configured to secure the second end of the body to an external anchor point,d.) the medical conduit protection device inhibiting tampering with or damage to the one or more medical conduits within the lumen of the body by transferring externally-applied strain away from the one or more medical conduits within the lumen thereof.2. The medical conduit protection device of claim 1 , wherein the body is a substantially continuous tubular structure claim 1 , adapted and configured to receive one or more medical conduits through the lumen thereof.3. The medical conduit protection device of claim 2 , wherein the body is formed from a resilient material which is resistant to plastic deformation.4. The medical conduit protection device of claim 2 , wherein the body is formed from a nonwoven fabric.5. The medical conduit protection device of claim 2 , ...

APPARATUS, SYSTEM AND METHOD FOR A DISSOLVABLE VALVE MEMBER

A valve assembly is provided which includes a housing having an inlet end and an outlet end and defining a fluid channel and a central chamber. A dissolvable valve member is positioned to obstruct flow through the channel within the chamber. The dissolvable valve member is formed of a material which is dissolvable at a predetermined rate upon contact with a preselected fluid. The preselected fluid is selected from the group consisting of blood, urine, saline and antimicrobial solutions. The dissolvable valve member can be formed from a fluid soluble glass or a starch based material. 120-. (canceled)21. A valve assembly configured to employ with a urinary catheter , the valve assembly comprising:a housing having an inlet end and an outlet end and defining a fluid channel and a central chamber, the inlet end dimensioned to releasably receive an outlet end of the urinary catheter; anda dissolvable valve member positioned to prevent flow through the channel in its undissolved state, the dissolvable valve member being formed of a material and being configured with dimensions and in a shape to dissolve and automatically open the flow through the channel following a pre-determined time-period during which the dissolvable valve member is in contact with a preselected fluid.22. The valve assembly of claim 21 , wherein the dissolvable valve member includes an inlet side claim 21 , an outlet side claim 21 , a central axis and a region proximate the central axis claim 21 , andwherein the region proximate the central axis is a location of a minimum thickness of the dissolvable valve member between the inlet side and the outlet side.23. The valve assembly of claim 22 , wherein at least one of the inlet side and the outlet side define a concavity.24. The valve assembly of claim 23 , wherein each of the inlet side and the outlet side define a spherical concavity.25. The valve assembly of claim 22 , wherein the dissolvable valve member is constructed such that a thickness of the ...

SHIELD APPARATUS

Apparatus () for shielding a catheter from contact with water whilst showering, the apparatus () comprising: a first shield component (()) having a first part () that is configured to form a first seal around an exit aperture () from which a catheter exits the patient's body, said first part () defining an internal volume () that opens to an internal volume () of a second part () that is configured to receive a distal part of said catheter; and a second shield component () for adhering to the patient's body around at least part of the periphery of the first part () of said first shield component (()) so as to provide a second seal against water contact with said exit aperture (); wherein said first and second shield components ((), ()) cooperate, when the apparatus () is worn by a patient, to resist water contact with said exit aperture () without obstructing access to an area of the patient's skin beneath said second part () of said first shield component (). 1. Apparatus for shielding a catheter from contact with water whilst showering , the apparatus comprising:a first shield component having a first part that is configured to form a first seal around an exit aperture from which a catheter exits the patient's body, said first part defining an internal volume that opens to an internal volume of a second part that is configured to be suitable for receiving a distal part of said catheter; anda second shield component for adhering to the patient's body around at least part of the periphery of the first part of said first shield component so as to provide a second seal against water contact with said exit aperture;wherein said first and second shield components cooperate, when the apparatus is worn by a patient, to resist water contact with said exit aperture without obstructing access to an area of the patient's skin beneath said second part of said first shield component.2. The apparatus of claim 1 , wherein the second shield component is configured to at least ...

Catheter Assembly

A catheter assembly () comprising a catheter () having a proximal end () adapted to be inserted into a bodily cavity and a distal end () having a drainage outlet (), a catheter package () having a cavity for accommodating the catheter and an opening for withdrawing the catheter from the package, and extracting means () that are coupled to the catheter for extracting the distal end of the catheter out of the package. 1. A catheter assembly comprisinga catheter having a proximal end adapted to be inserted into a bodily cavity and a distal end having a drainage outlet,a catheter package having a cavity for accommodating the catheter and an opening for withdrawing the catheter from the package, andextracting means that are coupled to the catheter for extracting the distal end of the catheter out of the package, wherein the extracting means are coupled to a part of the catheter that is distal to the proximal end and proximal to the distal end.2. A catheter assembly according to claim 1 , wherein the drainage outlet has a cross sectional diameter that is larger than the part of the catheter proximal to the drainage outlet.3. A catheter assembly according to claim 1 , wherein the extracting means are arranged in a distal end of the catheter package.4. A catheter assembly according to claim 1 , wherein the extracting means are coupled to a distal part of the catheter that is approximately between 50-99 percent of the length of the catheter.5. A catheter assembly according to claim 1 , wherein the extracting means is in the form of a strip that has at least a length that extends from a proximal end coupled to a coupling area of the catheter and a distal end abutting the opening of the catheter package.6. A catheter assembly according to claim 1 , where the extracting means are in the form of a strip having a proximal end that surrounds the catheter and a distal free end.7. A catheter assembly according to claim 6 , wherein the proximal end of the strip that surrounds the ...

CATHETER AND METHOD FOR ITS USE

The present invention discloses a catheter and method of using a catheter with two balloons and at least one inlet opening located on the proximal end of the catheter. The two balloons are adapted to retain the catheter within the body cavity and facilitate the flow of gases and fluids into one or more inlet openings. The invention also provides inlet openings located at different levels of the catheter tube to allow for complete drainage of fluid from the body cavity. The unique design of the present invention provides complete drainage of a body cavity and reduces damage and trauma to the body cavity. 1. An apparatus for insertion into a body cavity , comprising:a catheter of predetermined length and width having an open distal end and a closed proximal end; a main lumen and two secondary lumens extending longitudinally from the open distal end to the closed proximal end; the open distal end having at least one outlet port interconnected with the main lumen and at least two infusion ports interconnected with the two secondary lumens; the proximal end having at least one inlet and two balloons, wherein the two balloons are located 1-3 cm from the closed proximal end and are configured to expand perpendicularly along a longitudinal axis of the catheter.2. The catheter of wherein the catheter is comprised of a plurality of inlets on said proximal end.3. The catheter of wherein the catheter is an indwelling urinary catheter.4. The catheter of wherein at least one of the two balloons is about 5 mL.5. The catheter of wherein the two balloons are located at about equal distances from the closed proximal end.6. A catheter system comprising:a flexible tube of predetermined length and width having an open distal end with at least one infusion port and at least one outlet port and a closed proximal end with at least one inlet; andtwo retention members on the closed proximal end, wherein the retention members are located at equal distances 1-3 cm from the closed proximal end ...

SECUREMENT DEVICE

A securement device holds a medical article having flexible portions in position upon the body of a patient and inhibits movement of the medical article. The medical article may be insertable into the securement device from above, from below, or along a longitudinal axis of the device. The securement device may have abutment surfaces which interact with the flexible portions of the medical article to further inhibit rotation of the device. 1. A securement device for securing a medical article , the securement device comprising:first and second anchor pads, each comprising an upper foam layer and a lower adhesive surface, the lower adhesive surface being configured to attach to an epidermal layer of a patient; and a body member having an inverted channel formed therethrough, the inverted channel being configured to retain a portion of the medical article and having a longitudinal access opening disposed on an underside of the body member to allow ingress and egress of the portion of the medical article,', 'first and second anchor pads underlying the body member and laterally offset in opposite directions from the longitudinal access opening,', 'first and second proximal members extending generally transversely downward from the body member and defining a proximal retention surface therebetween, wherein the first proximal member terminates in a first proximal footing which is secured to the first anchor pad and the second proximal member terminates in a second proximal footing secured to the second anchor pad,', 'first and second distal members extending generally transversely downward from the body member and defining a distal retention surface therebetween, wherein the first proximal member terminates in a first distal footing which is secured to the first anchor pad, and wherein the second proximal member terminates in a free end unsecured to an anchor pad, and', 'an offset member extending laterally outward and longitudinally proximal from a point on the body ...

MULTI-LAYER MEDICAL DRESSINGS

A multi-layer dressing is disclosed. The dressing includes at least a primary layer comprised of a first layer, a transparent layer and a release liner. The first layer has an opening therethrough. The transparent layer is configured to cover the opening in the first layer. At least one of the first layer and the transparent layer includes a bottom adhesive surface. The release liner is attached to at least a portion of the bottom adhesive surface. The release liner is configured to provide an unobstructed view through the opening when the release liner is attached to the bottom adhesive surface. An optional closure piece is also disclosed, wherein the closure piece may be selectively altered to accommodate various sized catheter devise. 1. A multi-layer dressing , comprising:a first layer having an opening therethrough;a transparent layer configured to cover the opening in the first layer;wherein at least one of the first layer and the transparent layer includes a bottom adhesive surface; anda release liner attached to at least a portion of the bottom adhesive surface, wherein the release liner is configured to provide an unobstructed view through the opening when the release liner is attached to the bottom adhesive surface.2. The multi-layer dressing of claim 1 , further comprising a reinforcing element operatively connected to the first layer.3. The multi layer dressing of claim 2 , wherein the first layer includes a viewing portion and an anchor portion claim 2 , wherein the opening is formed in the viewing portion and wherein the reinforcing element is disposed on the anchor portion.4. The multi-layer dressing of claim 1 , further comprising pad member claim 1 , wherein the pad member is secured to the bottom adhesive surface such that the pad member is configured to contact a patient's skin.5. The multi-layer dressing of claim 4 , wherein the pad member is disposed at least partially about the opening in the first layer.6. The multi-layer dressing of claim 5 , ...

Stretch Valve Balloon Catheter and Methods for Producing and Using Same

A safety catheter for draining a given fluid includes a hollow stretch valve and a flexible, multi-lumen, balloon drainage catheter having a proximal catheter end, a balloon defining a balloon interior to be inflated with an inflation fluid, a drain lumen. and a balloon drainage port fluidically connecting the balloon interior to the drain lumen. The hollow stretch valve is shaped to permit the given fluid to pass therethrough and is positioned in the drain lumen to at least partially slide therein such that, in a steady state, the stretch valve prevents the inflation fluid from passing through the drainage port, and, in a stretched state when the proximal catheter end is stretched, the distal sliding portion slides within the drain lumen to permit the inflation fluid to pass through the drainage port and into the drain lumen. 1. A safety catheter , comprising: a drain lumen extending through the shaft and shaped to drain fluid adjacent the distal tip therethrough and out the drain end;', 'a distal hollow balloon portion defining a balloon interior and having at least one inflation port fluidically connected to the balloon interior, the balloon portion inflating outwardly to a diameter greater than the outer diameter of the shaft when inflated with inflation fluid;', 'at least one inflation lumen parallel to the drain lumen and fluidically connected to the balloon interior through the at least one inflation port, the at least one inflation lumen shaped to inflate the balloon interior with the inflation fluid; and', 'a drainage port fluidically connecting the balloon interior to the drain lumen; and, 'a flexible, multi-lumen shaft having an outer diameter, a distal tip, and a proximal catheter end with a drain end, the multi-lumen shaft defining coaxially disposed in the drain lumen and shaped to permit fluid to pass therethrough;', 'having a distal sliding portion slidably disposed within the drain lumen;', in a steady state, the stretch valve prevents the inflation ...

Stretch Valve Balloon Catheter and Methods for Producing and Using Same

A safety balloon catheter includes a stretch valve and a balloon catheter having a proximal catheter end, a balloon defining an interior to be inflated with an inflation fluid, an inflation lumen extending through the shaft to the interior and shaped to convey inflation fluid thereto and from, a second lumen parallel to the inflation lumen, and a balloon drainage port fluidically connecting the balloon interior to the second lumen. The hollow stretch valve is shaped to permit a fluid to pass therethrough and is positioned in the second lumen to at least partially slide therein such that, in a steady state, the stretch valve prevents the inflation fluid from passing through the drainage port and, in an over-inflated state, the distal sliding portion slides within the second lumen to permit the inflation fluid to pass through the drainage port and into the second lumen. 1. A safety balloon catheter , comprising: a proximal catheter end;', 'a balloon defining a balloon interior to be inflated with an inflation fluid;', 'a hollow inflation lumen extending through the catheter to the balloon interior and shaped to convey the inflation fluid to and from the balloon interior;', 'a hollow second lumen parallel to the inflation lumen; and', 'a balloon drainage port fluidically connecting the balloon interior to the second lumen;, 'a flexible, multi-lumen balloon catheter having shaped to permit a fluid to pass therethrough; and', in a steady state, the stretch valve prevents the inflation fluid from passing through the drainage port; and', 'in an over-inflated state, the distal sliding portion slides within the second lumen to permit the inflation fluid to pass through the drainage port and into the second lumen., 'positioned in the second lumen to at least partially slide therein such that], 'a hollow stretch valve2. The safety catheter according to claim 1 , wherein:the balloon catheter has a shaft outer diameter; andthe balloon is inflatable outwardly to a diameter ...