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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 12084. Отображено 100.
19-01-2012 дата публикации

Tracheostomy valves and related methods

Номер: US20120012116A1
Принадлежит: Passy Muir Inc

The embodiments of the present tracheostomy valves include a flexible diaphragm abutting a rib shaped substantially as a flat plate. Opposite the rib, the diaphragm abuts a boss and forms an uninterrupted seal therewith. As the tracheostomized patient inhales, the diaphragm bends about the rib, interrupting the seal and allowing air to flow smoothly into the valve. The features of the various embodiments contribute to a positive seal at all times except during inhalation, and low resistance to airflow through the valve during inhalation.

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05-04-2012 дата публикации

Visual indicator for an aerosol medication delivery apparatus and system

Номер: US20120080028A1
Принадлежит: TRUDELL MEDICAL INTERNATIONAL

A delivery system includes a holding chamber with first, second and third openings, and independently moveable first, second and third flow control members. A delivery system includes a holding chamber and a flow control member including a flap pivotable from an at rest position in a direction toward an outlet of a user interface and away from an output end of the holding chamber in response to a pressure being applied thereto.

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14-06-2012 дата публикации

Adhesive and peripheral systems and methods for medical devices

Номер: US20120150115A1
Принадлежит: Deka Products LP

Fill stations and base stations are provided for personal pump systems. The fill stations may be opened and closed to accept a reservoir and to allow fluid to be introduced into the reservoir for use with personal pump systems. The fill stations may hold the reservoir at a tilt relative to an underlying surface and may discourage overfilling of the reservoir. The filling stations may also include viewing windows having fluid lines marked thereon for indicating volume of fluid within the reservoir.

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12-07-2012 дата публикации

Structural hydrogel polymer device

Номер: US20120178874A1
Автор: Scott M. Epstein
Принадлежит: Individual

The present invention relates generally a manufacturing process which results in a completely hydrogel polymer device that maintains lumen patency which allows for numerous applications. Catheters and stents are particular examples, and their composition, mechanical characteristics, and the significantly unique ability to conduct and allow fluids to pass from one end to the other without physiological rejection, inflammation, or manifestation of complications due to implant or otherwise undesirable outcomes when used for ambulatory and or therapeutic interventions is the purpose of the invention.

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16-08-2012 дата публикации

Patch-sized fluid delivery systems and methods

Номер: US20120209179A1
Принадлежит: Deka Products LP

A patch-sized fluid delivery device may include a reusable portion and a disposable portion. The disposable portion may include components that come into contact with the fluid, while the reusable portion may include only components that do not come into contact with the fluid. Redundant systems, such as redundant controllers, power sources, motor actuators, and alarms, may be provided. Alternatively or additionally, certain components can be multi-functional, such a microphones and loudspeakers that may be used for both acoustic volume sensing and for other functions and a coil that may be used as both an inductive coupler for a battery recharger and an antenna for a wireless transceiver. Various types of network interfaces may be provided in order to allow for remote control and monitoring of the device.

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16-08-2012 дата публикации

Adhesive and peripheral systems and methods for medical devices

Номер: US20120209207A1
Автор: Eric Yeaton, Larry B. Gray
Принадлежит: Deka Products LP

A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

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13-09-2012 дата публикации

Systems and methods to compensate for compression forces in an intravascular device

Номер: US20120232498A1
Автор: Marty L. Stout, Yiping Ma
Принадлежит: Becton Dickinson and Co

A system and method for providing vent channel geometries to compensate for compression forces experienced by a septum within an intravascular device.

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04-10-2012 дата публикации

Blister Package for Pharmaceutical Cartridges

Номер: US20120248005A1
Автор: Michael S. Bergey
Принадлежит: MANNKIND CORP

A blister packaging for a pharmaceutical cartridge or capsule is disclosed.

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29-11-2012 дата публикации

Pneumatic injector

Номер: US20120302992A1

This document discloses, among other things, an air-powered auto-injector device for subcutaneous delivery of a rescue drug. The device is configured for self-administered treatment of anaphylactic shock. Air is compressed by relative movement of a piston and a cylinder and released to subcutaneously drive an hypodermic needle.

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28-02-2013 дата публикации

Space-efficient containment devices and method of making same

Номер: US20130053671A1
Автор: Robert Farra
Принадлежит: MicroChips Inc

Containment devices and methods of manufacture and assembly are provided. In an embodiment, the device includes at least one microchip element, which includes a containment reservoir that can be electrically activated to open, and a first electronic printed circuit board (PCB) which comprises a biocompatible substrate. The first PCB may have a first side on which one or more electronic components are fixed and an opposed second side on which the microchip element is fixed in electrical connection to the one or more electronic components. The device may further include a second PCB and a housing ring securing the first PCB together with the second PCB. The microchip element may include a plurality of containment reservoirs, which may be microreservoirs, and/or which may contain a drug formulation or a sensor element.

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21-03-2013 дата публикации

Device and method for treating central nervous system pathology

Номер: US20130072827A1
Принадлежит: Wake Forest University Health Sciences

The present invention relates generally to a device and method for treating tissues of the central nervous system and more particularly, but not exclusively, to a device and method for treating the brain tissue.

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30-05-2013 дата публикации

Syringe with needle

Номер: US20130138047A1
Принадлежит: Terumo Corp

This syringe with needle is provided with a needle tube having a needle tip capable of puncturing a living body, and a syringe by insert molding formed integrally with the needle tube. The syringe includes: a main body which is filled with a drug; and a securing section which is formed to be continuous with the main body. The securing section secures the needle tube in a state that the needle tip of the needle tube is protruded. The securing section of the syringe includes a holding hole in which a chuck member for supporting and securing a circumferential surface of the needle tube during the insert molding is inserted and passed.

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20-06-2013 дата публикации

Tracheal tube adaptor and flaring jig

Номер: US20130152355A1
Принадлежит: COVIDIEN LP

The present disclosure describes systems and methods that utilize a tracheal tube adaptor system. The tracheal tube adaptor system includes a tracheal tube adaptor and/or a flaring jig. A proximal end of a tracheal tube may be flared and the tracheal tube adaptor may be coupled to the proximal end of the tracheal tube. The tracheal tube adaptor may be configured to easily attach and detach an end connector. The end connector may be used to couple a variety of medical devices such as a ventilator, a manual respirator, a nebulizer, a vaporizer, suctioning equipment, and so forth, to the tracheal tube. The use of the tracheal tube adaptor system and methods enables the rapid detachment and attachment of various end connectors, thus allowing the coupling of the tracheal tube to a variety of medical devices.

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01-08-2013 дата публикации

Assembling a needleless valve system

Номер: US20130193359A1
Автор: Jonathan Yeh
Принадлежит: CareFusion 303 Inc

A base portion for a needleless valve system comprising a body, and a valve coupling feature disposed on the body. The valve coupling feature is configured for coupling to a base coupling feature of a valve of a first type and a base coupling feature of a valve of a second type.

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01-08-2013 дата публикации

Reduced-pressure dressing assemblies for use in applying a closing force

Номер: US20130197457A1
Принадлежит: Kci Licensing Inc

A closing dressing bolster and assembly for use with a system for treating a linear wound on a patient includes a bolster body formed from a flexible closing bolster material having closing members that are operable to develop an inward closing force when the closing dressing bolster is placed under reduced pressure. In one aspect, when the closing dressing bolster is under reduced pressure, the system, dressing, or assembly develops an inward force realized at the linear wound and a compression force. A wicking-material holder and wicking material may be used as well. The member components may all be see-through to allow visual inspection of the wound without requiring removal of the dressing.

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08-08-2013 дата публикации

Drug delivery device and method for assembling a drug delivery device

Номер: US20130204183A1
Принадлежит: Sanofi Aventis Deutschland GmbH

A drug delivery device comprises a first component and a second component, wherein a substance is provided on at least one of the first component and the second component. An inner friction of the substance is great enough to stabilize at least one of the orientation and the position of the first component and the second component with respect to one another. The inner friction of the substance is small enough to allow relative movement of the first component and the second component necessary for the intended operation of the device. Furthermore, a method for assembling a drug delivery device is provided.

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15-08-2013 дата публикации

Microfabricated nanopore device for sustained release of therapeutic agent

Номер: US20130211368A1
Принадлежит: Delpor Inc

A drug delivery device that includes a capsule for implantation into the body; the capsule further includes a reservoir for containing a substance such as a therapeutic agent, at least one port for allowing the substance to diffuse from or otherwise exit the reservoir, and a nanopore membrane in communication with the capsule at or near the exit port for controlling the rate of diffusion of the substance from the exit port. The device also includes an optional screen for providing structural stability to the nanopore membrane and for keeping the pores of the nanopore membrane clear. One embodiment of the drug delivery device includes an osmotic engine internal to the device for creating fluid flow through the device.

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31-10-2013 дата публикации

Apparatus and methods for filling a drug eluting medical device via capillary action

Номер: US20130284311A1
Принадлежит: Medtronic Vascular Inc

Methods and apparatus are disclosed for filling a therapeutic substance or drug within a hollow wire that forms a stent. The stent is placed within a chamber housing a fluid drug formulation. During filling, the chamber is maintained at or near the vapor-liquid equilibrium of the solvent of the fluid drug formulation. To fill the stent, a portion of the stent is placed into contact with the fluid drug formulation until a lumenal space defined by the hollow wire is filled with the fluid drug formulation via capillary action. After filling is complete, the stent is retracted such that the stent is no longer in contact with the fluid drug formulation. The solvent vapor pressure within the chamber is reduced to evaporate a solvent of the fluid drug formulation. A wicking means may control transfer of the fluid drug formulation into the stent.

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14-11-2013 дата публикации

Vented dispensing device and method

Номер: US20130304018A1
Автор: Avraham Neta, Ofer Yodfat
Принадлежит: MEDINGO LTD

Disclosed is a fluid dispensing device that includes at least one reservoir to hold the therapeutic fluid, at least one other unit requiring communication with ambient air, at least partly, to operate, and at least one housing defining an interior to retain the at least one reservoir and the at least one other unit. The at least one housing has at least one vent port formed on one or more of its walls. The at least one vent port is adapted to direct or communicate air to maintain pressure equilibrium between the air pressure in the interior of the at least one housing and the ambient air pressure outside the at least one housing, and provide communication with the ambient air to the at least one other unit requiring air to enable operation of the at least one other unit.

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12-12-2013 дата публикации

Systems for treating pulmonary infections

Номер: US20130330400A1
Принадлежит: Insmed Inc

Provided herein are systems for treating a subject with a pulmonary infection, for example, a nontuberculous mycobacterial pulmonary infection, a Burkholderia pulmonary infection, a pulmonary infection associated with bronchiectasis, or a Pseudomonas pulmonary infection. The system includes a pharmaceutical formulation comprising a liposomal aminoglycoside dispersion, and the lipid component of the liposomes consist essentially of electrically neutral lipids. The system also includes a nebulizer which generates an aerosol of the pharmaceutical formulation at a rate greater than about 0.53 gram per minute. The aerosol is delivered to the subject via inhalation for the treatment of the pulmonary infection.

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12-12-2013 дата публикации

Autoinjectors

Номер: US20130331796A1
Автор: Robert Wozencroft
Принадлежит: OWEN MUMFORD LTD

An autoinjector includes a body ( 10, 12 ), a syringe carrier ( 34 ) supporting a syringe ( 13 ) or cartridge with a needle at its forward end, for movement from a rearward position to a forward position to extend a needle, the syringe or cartridge having a barrel of generally cylindrical form having at a forward region thereof a forward facing abutment surface, wherein the syringe carrier is provided with a retention surface arranged to cooperate with the forward facing abutment surface on the syringe to prevent or limit forward movement of the syringe relative to the syringe carrier, the autoinjector further including a removable needle shield ( 15 ) releasably attached to the syringe or cartridge and shrouding the needle, a cap ( 14 ) attached to the forward end of the body and forwardly removable, the cap having a removal surface for engaging the needle shield whereby removal of the cap removes the needle shield.

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23-01-2014 дата публикации

Patch-sized fluid delivery systems and methods

Номер: US20140025001A1
Принадлежит: Deka Products LP

A patch-sized fluid delivery device may include a reusable portion and a disposable portion. The disposable portion may include components that come into contact with the fluid, while the reusable portion may include only components that do not come into contact with the fluid. Redundant systems, such as redundant controllers, power sources, motor actuators, and alarms, may be provided. Alternatively or additionally, certain components can be multi-functional, such a microphones and loudspeakers that may be used for both acoustic volume sensing and for other functions and a coil that may be used as both an inductive coupler for a battery recharger and an antenna for a wireless transceiver. Various types of network interfaces may be provided in order to allow for remote control and monitoring of the device.

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06-02-2014 дата публикации

Drug delivery device for delivery of a medicament

Номер: US20140039412A1
Автор: Axel Forstreuter
Принадлежит: Sanofi Aventis Deutschland GmbH

Various embodiments of drug delivery devices and methods of assembling such devices are provided. In one embodiment, a drug delivery device for dispensing medicament comprises a medicament cartridge, wherein the cartridge comprises (i) a distal end, (ii) a proximal end that is opposite the distal end along a body axis of the cartridge, and (iii) a movable piston arranged substantially at the proximate end of the cartridge. The drug delivery device further comprises a piston rod having a distal end for axially moving the piston in the distal direction during dispensing of a set dose of medicament, wherein a relative axial distance between the distal end of the piston rod and a proximal face of the piston is set during assembly of the drug delivery system. The relative axial position between may be set such that the piston rod and the proximal face of the piston abut each other.

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06-03-2014 дата публикации

Cartridge Holder and Method for Assembling a Cartridge Unit for a Drug Delivery Device

Номер: US20140066863A1
Автор: Philippe Nzike
Принадлежит: Sanofi Aventis Deutschland GmbH

A cartridge holder for retaining a cartridge comprising a distal end and a proximal end being spaced apart from one another in the direction of an axis, an interior which is suitable to receive and retain a cartridge in a cartridge retaining section of the interior, and a main part and at least one protrusion which is moveably connected to the main part. The protrusion is arranged to define the radial extension of a subsection of the interior, wherein the subsection is arranged at an axial position which is further away from the distal end than the cartridge retaining section. Furthermore, the protrusion is arranged to vary the radial extension of the subsection when the protrusion is moved with respect to the main part. Moreover, a method for securing a cartridge in a cartridge holder is proposed.

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06-03-2014 дата публикации

Inflatable medical devices

Номер: US20140066896A1
Принадлежит: Loma Vista Medical Inc

An inflatable structure for use in biological lumens and methods of making and using the same are disclosed. The structure can have an inflatable balloon encircled by a shell. The shell can have proximal and distal tapered necks, longitudinally-oriented flutes, and apertures at the proximal and distal ends of the shell. The apertures can be recessed in the flutes in the necks. The shell can also have fiber reinforced walls.

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10-04-2014 дата публикации

Dose counters for inhalers, inhalers and methods of assembly thereof

Номер: US20140096769A1
Принадлежит: Norton Waterford Ltd

A manually operated metered dose inhaler includes a dose counter chamber including a dose display tape driven by a ratchet wheel which is driven in turn by an actuator pawl actuated by movement of a canister, the tape unwinding from a stock bobbin during use of the inhaler, a rotation regulator being provided for the stock bobbin and including a wavelike engagement surface with concavities which engage against control elements in the form of protrusions on resilient forks of a split pin thereby permitting incremental unwinding of the stock bobbin yet resisting excessive rotation if the inhaler is dropped onto a hard surface.

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04-01-2018 дата публикации

VIA AND TRENCH FILLING USING INJECTION MOLDED SOLDERING

Номер: US20180000412A1
Принадлежит:

A method includes forming one or more trenches in a first substrate, forming one or more vias in a second substrate, aligning at least a first trench in the first substrate with at least a first via in the second substrate, and sealing the first substrate to the second substrate by filling the first via and the first trench with solder material using injection molded soldering. 1. A method comprising:forming one or more trenches in a first substrate;forming one or more vias in a second substrate;aligning at least a first trench in the first substrate with at least a first via in the second substrate;depositing a delivery substance in a reservoir formed in the second substrate; andbonding the first substrate to the second substrate by filling the first via and the first trench with solder material using injection molded soldering, wherein bonding the first substrate to the second substrate seals the delivery substance between the first substrate and the second substrate.2. (canceled)3. The method of claim 1 , wherein bonding the first substrate to the second substrate hermetically seals the delivery substance between the first substrate and the second substrate.4. The method of claim 1 , wherein the delivery substance comprises a medical substance.5. The method of claim 1 , wherein the delivery substance comprises a biological sensor.6. The method of claim 1 , wherein the delivery substance comprises an electronic device.7. The method of claim 1 , wherein the first trench surrounds the reservoir.8. The method of claim 7 , further comprising forming a first thermal insulator layer between the first trench and the reservoir.9. The method of claim 8 , further comprising forming a second thermal insulator layer in the second substrate claim 8 , wherein aligning the first trench in the first substrate with the first via in the second substrate further comprises aligning the first thermal insulator layer and the second thermal insulator layer claim 8 , and wherein bonding ...

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06-01-2022 дата публикации

INJECTION DEVICE WITH A CAP FOR REMOVING A NEEDLE SHIELD CAP FROM A PRODUCT CONTAINER, AND METHOD FOR ASSEMBLING SUCH AN INJECTION DEVICE

Номер: US20220001113A1
Принадлежит:

Injection devices include a cap for removing a needle shield cap from a product container, and methods for assembling such injection devices, involve providing a cap that includes an engagement element for use in removing the needle shield cap from the product container when the cap is removed from the injection device. 1. An injection device with a longitudinal axis , comprising:a housing for receiving a product container, wherein the product container includes an injection needle fixedly connected thereto and a needle shield cap detachably arranged on the product container, the needle shield cap enclosing the injection needle and sealing the injection needle from the environment in a sterile manner; anda cap detachably connected to a distal end of the housing, wherein the cap comprises an engagement element for removing the needle shield cap from the product container when the cap is removed from the injection device, wherein the engagement element is deformable such that the engagement element is movable from a spaced-apart position in which the engagement element is radially spaced from the needle shield cap to an engagement position in which the engagement element is in an engagement with the needle shield cap, wherein the engagement element is deformed during cap removal,wherein the cap comprises a sleeve element, the sleeve element comprising a recess having a distal edge and a proximal edge, wherein the engagement element is arranged in the spaced-apart position by the distal edge of the recess, and wherein the engagement element is moved to the engagement position by the proximal edge of the recess.2. The injection device according to claim 1 , wherein the sleeve element comprises a grip element to be gripped by a user.3. The injection device according to claim 1 , wherein the sleeve element and the engagement element are axially movable relative to one another when the engagement element is in the spaced-apart position.4. The injection device according to ...

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06-01-2022 дата публикации

CATHETER DEVICES WITH BLOOD CONTROL SYSTEMS AND RELATED METHODS

Номер: US20220001145A1
Принадлежит:

Needle assemblies and related methods having a needle hub with a needle, a catheter tube with a catheter hub and having the needle extending through the catheter tube, a valve positioned in an interior cavity of the catheter hub, a valve opener proximal of the valve, and a needle guard extending at least partially into the valve opener. The valve opener can be used with a range of needle sizes. 1. A needle assembly comprising:a needle hub with a needle having a needle shaft and a needle tip extending from a distal end of the needle hub;a catheter hub having an interior surface defining an interior cavity;a catheter tube attached to the catheter hub and having the needle extending through the catheter tube with the needle tip extending out a distal opening in a ready to use position;a valve comprising a plurality of slits and a plurality of flaps defining an opening seated in the interior cavity of the catheter hub;a needle guard comprising at least one arm extending from a proximal wall having a perimeter defining a proximal opening;a valve opener positioned in the interior cavity of the catheter hub and proximal of the valve in a first position, the valve opener comprising a head located distally of the needle guard and two valve opener arms extending in a proximal direction of the head and located in between the needle guard and the interior surface of the catheter hub, each of said two valve opener arms comprising a clip seat having the needle guard biased there against and having a width measured orthogonally to the needle shaft, and wherein the width of the clip seat is larger than a diameter of the needle shaft and larger than a range of diameters of needle shafts in which the diameter of the needle shaft falls into; andwherein the head of the valve opener is axially displaceable against the valve to open the valve in a second position.2. The needle assembly according to claim 1 , wherein the needle guard engages a guard engagement section formed on the ...

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01-01-2015 дата публикации

HEAD HARNESS FOR POSITIONING A PATIENT INTERFACE

Номер: US20150000671A1
Принадлежит:

Disclosed is a set of holding arrangements for a head harness in the region of a patient interface. The set comprises at least two holding arrangements which are distinguishable by identification markings and/or codings and are unambiguously assignable. 1. A set of holding arrangements for a head harness in a region of a patient interface , wherein the set comprises at least two holding arrangements which are distinguishable by identification markings and/or codings and are unambiguously assignable.2. The set of claim 1 , wherein the at least two holding arrangements are configured differently for upper and lower halves of the patient interface.3. The set of claim 1 , wherein the at least two holding arrangements are configured differently for right and left halves of the patient interface.4. The set of claim 1 , wherein the set comprises a plurality of holding elements which serve to connect the head harness to the patient interface at at least two contact points.5. The set of claim 4 , wherein at least two of the holding elements comprise a geometric and/or colored confusion prevention element which enables assignment of the harness to corresponding mounts in the patient interface unambiguously and with no risk of confusion.6. The set of claim 1 , wherein harness clips are pre-fitted on lower harness tabs of the head harness and are connected inseparably to textile material by end stoppers which fit over ends of the harness tabs and are at least one of sewn claim 1 , adhesively bonded or welded there.7. The set of claim 1 , wherein harness clips are pre-fitted on lower harness tabs in a cheek region and are connected to textile material by end stoppers which claim 1 , following pre-fitting of the harness clips claim 1 , can be inserted into an orifice.8. The set of claim 1 , wherein a harness clip pre-fitted on a harness tab latches in an adapter on a mask body.9. The set of claim 1 , wherein the identification markings of a harness clip and adapter have been ...

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01-01-2015 дата публикации

Nasal cannula assembly with inhalation valves communicating with a deformable reservoir

Номер: US20150000673A1
Автор: Andrew Martin

The invention concerns a nasal cannula assembly ( 10 ) adapted to deliver gases to a patient comprising a first compartment ( 1 ) and a second compartment ( 2 ) separated by a separation wall ( 6 ); a pair of nasal prongs ( 5 ) in fluid communication with the first compartment ( 1 ); the first compartment ( 1 ) comprising a first inlet ( 11 ) for introducing a first gas into said first compartment ( 1 ); the second compartment ( 2 ) comprising a second inlet ( 2 ) for introducing a second gas into said second compartment ( 2 ); and the separation wall ( 6 ) comprising at least one valve element ( 3 ) for controlling the passage of gas from the second compartment ( 2 ) to the first compartment ( 1 ). The invention concerns also a breathing assistance apparatus comprising a source of NO gas, and said nasal cannula assembly ( 10 ) in fluid communication with said source of NO gas.

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07-01-2021 дата публикации

INTRA-RUMINAL DEVICE

Номер: US20210000580A1
Принадлежит:

The invention relates to an intra-ruminal device comprising a cap, with outlet, that overlaps a portion of the barrel to define an attachment zone. Located within the attachment zone is at least one protrusion providing a localised point of contact between the barrel wall and the internal sidewall of the cap to provide for an ultrasonic weld between the barrel and the cap. Optionally the plunger comprises at least one aperture to allow fluid or gas communication between first and second compartments in the barrel. Optionally included are at least one pair of resilient wings, each pair of wings having a pair of reinforcement ridge that extend a first distance from the body along the wing surface, and at least one middle reinforcement ridge that extends between the pair of ridges from the body a second distance, and where the second distance is less than the first distance. 1. An intra-ruminal device comprisinga body substantially impervious to rumen fluids, the body defining a barrel having a first end and a second end, and an opening at the first end,at least one variable geometry device connected to and extending from the body to assist rumen retention,a dose of an active agent within the body to be accessible to rumen fluid via the first end,a biasing arrangement within the body adapted to bias a plunger against the active agent in the barrel towards the first end, anda cap having a sidewall and top, the cap located over the opening at the first end and comprising an outlet in the top;whereini) the cap has sidewalls that overlap a portion of the barrel to define an attachment zone, and located within the attachment zone is at least one protrusion providing a localised point of contact between a wall of the barrel and an internal portion of the sidewall of the cap to provide for an ultrasonic weld between the barrel and the cap at the attachment zone, orii) the plunger located in the barrel defines a first compartment holding the active agent between the plunger ...

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07-01-2016 дата публикации

TRANSFORMABLE INTRAVENOUS POLE AND BOOM COMBINATION AND METHOD THEREOF

Номер: US20160000995A1
Принадлежит:

An intravenous (IV) pole docking system for supporting medical equipment having a mast engaged to a base, the base having legs to support the mast and a lifting mechanism engaged to the base and the mast for moving the base along the mast in combination with an extension arm meant to reduce the IV pole footprint. The boom/IV pole system can reduce excess obstacles in and around hospital bed, surgical rooms and the like. 1. A method of engaging a pole to a boom in a hospital room , the method comprising:providing a boom with at least one laterally extending arm and at least one downwardly extending arm attached to the laterally extending arm;attaching a pole with a base to the arm of the boom, the pole comprising a plurality of circumferentially spaced apart outwardly legs, each leg holding at least one respective wheel; thenmanually engaging a foot pedal of the pole; and thenautomatically retracting the plurality of legs and lifting the wheels off a floor in response to only the manually engaging action whereby the pole is suspended by the boom.2. The method of claim 1 , wherein the downwardly extending arm comprises an upper pole attachment member and a lower pole attachment member claim 1 , wherein the attaching the pole to the downwardly extending arm is carried out by sliding a narrow medial segment of the pole into a receiving channel of the upper pole attachment member so that an outwardly facing key member engages outer end portions of the upper pole attachment member to encase the narrow segment of the pole.3. The method of claim 2 , wherein the base of the pole resides a greater distance away from the upper pole attachment member during the attaching step than during the automatically retracting step such that the base rises toward the upper mount member to lock the pole to the downwardly extending arm of the boom also in response to the manually engaging step thereby providing a single user action to retract the legs claim 2 , lift and lock the pole to the ...

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07-01-2021 дата публикации

METHOD OF MANUFACTURING A BLOOD PUMP

Номер: US20210001027A1
Принадлежит:

An intravascular blood pump comprises a pumping device including an impeller and an electric motor for driving the impeller. A rotor of the electric motor is rotatable about an axis of rotation and coupled to the impeller so as to be able to cause rotation of the impeller. An outer sleeve forms a casing of the pumping device, wherein stator components are fixed inside the outer sleeve by means of a casting compound. In a method of manufacturing the blood pump the stator components are placed on a molding base, including the outer sleeve to thereby form an interspace between the molding base and the outer sleeve in which the stator components are disposed. The casting compound is then injected into the interspace via the molding base to fix the stator components inside the outer sleeve. The outer sleeve preferably comprises a magnetically conductive material to form a yoke of the electric motor. 1. A method of manufacturing an intravascular blood pump , the blood pump comprising a pumping device including an impeller and an electric motor for driving the impeller , the electric motor including a stator and a rotor , the rotor rotatable about an axis of rotation and coupled to the impeller so as to be able to cause rotation of the impeller , the method comprising the steps of:providing a molding base sized and shaped for receiving stator components thereon;placing the stator components on the molding base;placing an outer sleeve on the molding base to thereby form at least a portion of an outer surface of the blood pump and an interspace between the molding base and the outer sleeve in which the stator components are disposed; andinjecting a casting compound into the interspace via the molding base to fix the stator components inside the outer sleeve.2. The method according to claim 1 , wherein the outer sleeve comprises a magnetically conductive material to form a yoke of the electric motor.3. The method according to claim 2 , wherein the outer sleeve comprises a ...

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07-01-2021 дата публикации

Apparatus and method for filling solution bags for dialysis

Номер: US20210001029A1
Принадлежит: FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH

The present invention relates to an apparatus and to a method for filling a solution bag for dialysis with a liquid, wherein the apparatus comprises a needle for introduction into a filling line or filling opening of the bag, wherein the needle is a double wall needle having a preferably thermally conductive outer wall and having an inner wall, with a thermal insulation being present between the outer wall and the inner wall; and with a heating element being provided that is configured to heat the outer side of the outer wall to a temperature above the temperature of the inner side of the inner wall.

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07-01-2021 дата публикации

ASSEMBLY FOR AN INJECTION OR INFUSTION DEVICE

Номер: US20210001048A1
Принадлежит:

An assembly for an injection or infusion device includes i) a cartridge being closed by a septum and the surface of the septum being sterile and covered by a first continuous flexible strip, and ii) a fluid path unit comprising a cartridge holder and a fluid path compartment comprising a needle in an interior, the needle is configured to penetrate the septum of the cartridge through a passage in the fluid path compartment. The passage is closed by a second continuous flexible strip keeping the interior of the fluid path compartment in a sterile condition. The cartridge is inserted into the cartridge holder aligning the septum with the passage and sandwiching both strips between the septum and the fluid path compartment. Both strips may be simultaneously removable from the cartridge and fluid path compartment thereby, establishing a sterile connection between the septum and the interior of the fluid path compartment. 1. An assembly for an injection or infusion device comprising:a cartridge for a sterile liquid medicament formed as a barrel, the cartridge being closed by a septum fastened to the barrel by a crimp, wherein a surface of the septum opposite a surface contacting the liquid medicament being sterile and covered by a first area of a first continuous flexible strip attached to the crimp, thereby keeping the opposite surface of the septum in a sterile condition; anda fluid path unit comprising a cartridge holder and a fluid path compartment comprising a needle or spike in an interior of the fluid path compartment, wherein the needle or spike is configured to penetrate the septum of the cartridge through a passage in the fluid path compartment, wherein the passage of the fluid path compartment is closed by a second continuous flexible strip attached to the fluid path compartment, the second continuous flexible strip comprising a second area covering the passage thereby keeping the interior of the fluid path compartment in a sterile condition,wherein the ...

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07-01-2021 дата публикации

CAP, SYRINGE ASSEMBLY AND MANUFACTURING METHOD THEREOF

Номер: US20210001049A1
Принадлежит: TERUMO KABUSHIKI KAISHA

A syringe assembly includes a plate-shaped seal member that seals a distal opening of a distal nozzle portion of a syringe; and a tubular cover member. The cover member has a base portion and a mounting portion. The mounting portion has two claw portions, two first column portions arranged on both sides of one of the two claw portions, and two second column portions arranged on both sides of the other of the two claw portions. An outer peripheral portion of the mounting portion has two outer peripheral notch portions. An inner peripheral portion of the mounting portion has two inner peripheral recessed portions. 1. A tubular cap mountable to a distal nozzle portion of a syringe , the cap comprising:a plate-shaped seal member that has elasticity and seals a distal opening of the distal nozzle portion; anda tubular cover member that holds the seal member and is harder than the seal member, whereinthe cover member has a base portion provided at a distal end of the cover member, and a tubular mounting portion that extends in a proximal direction from the base portion along an axis of the cap and covers the distal nozzle portion,the base portion has a holding portion that holds the seal member, and a through-hole that communicates with the holding portion and exposes a distal surface of the seal member,the mounting portion has:two claw portions that are arranged at positions separated from the holding portion in the proximal direction, protrude inward from an inner peripheral surface of the mounting portion, and oppose each other;two first column portions that are arranged on both sides of one of the two claw portions in a circumferential direction of the mounting portion and extend in the proximal direction along the axis of the cap; andtwo second column portions that are arranged on both sides of another of the two claw portions in the circumferential direction of the mounting portion and extend in the proximal direction along the axis of the cap,an outer peripheral ...

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07-01-2021 дата публикации

AIR DELIVERY CONDUIT

Номер: US20210001074A1
Автор: HENRY Robert Edward
Принадлежит:

An air delivery conduit for conveying breathable gas from a positive airway pressure device to a patient interface includes a tubular wall structure constructed from a textile material. A reinforcing structure may be provided to the wall structure that is structured to prevent kinking or collapsing of the wall structure. The wall structure may include a warp having a plurality of lengthwise textile warp threads arranged in a circle and a weft having a textile weft thread that is woven through the warp threads. 1. A conduit for conveying air from a respiratory device to a patient interface , wherein a portion of the conduit is made from a textile.2. A conduit as claimed in claim 1 , wherein the conduit includes a wall claim 1 , a portion of which is made from a textile.3. A conduit as claimed in any one of to claim 1 , further including a reinforcing structure claim 1 , wherein at least a portion of the reinforcing structure is made from a textile.4. A conduit as claimed in any one of to claim 1 , wherein the textile is a non-porous claim 1 , woven textile.5. A conduit as claimed in any one of or claim 1 , wherein the textile is a porous claim 1 , woven textile and is treated such that it is substantially non-porous.6. A conduit as claimed in any one of to claim 1 , wherein the textile is a woven textile claim 1 , manufactured by a circular weaving process.7. An air delivery conduit for conveying breathable gas from a positive airway pressure device to a patient interface claim 1 , comprising:a tubular wall structure constructed from a textile material;a reinforcing structure provided to the wall structure, the reinforcing structure structured to prevent kinking or collapsing of the wall structure.8. An air delivery conduit according to claim 7 , wherein the reinforcing structure includes a spiral or helical shape.9. An air delivery conduit according to any one of - claim 7 , wherein the reinforcing structure is constructed of plastic.10. An air delivery conduit ...

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07-01-2016 дата публикации

DRIVE MECHANISM FOR A DRUG DELIVERY DEVICE

Номер: US20160001009A1
Автор: Saiki Masaru
Принадлежит:

A drive mechanism for a drug delivery device having a rotationally fixed plunger rod driven by a lead screw. The lead screw engages a free lock which is coupled to a release knob. A dose setting dial cooperates with an inner cylinder using a clutch to establish the axial movement of the plunger rod during dose setting and dispensing. 1. A drive mechanism for use in a drug delivery device comprising:a housing having a proximal end, a distal end and an internal thread;a dose setting dial threadedly engaged with the internal thread and configured to simultaneously rotate and traverse axially towards the proximal end during dose setting and to simultaneously rotate and traverse axially towards the distal end during dose dispensing;a plunger rod rotatably fixed relative to the housing during both setting and dose dispensing, the plunger rod having a threaded hollow portion;a lead screw threadedly engaged with the threaded hollow portion such that the lead screw can rotate relative to the plunger rod;an inner cylinder engaged with and positioned within the dose setting dial such that axial movement of the dose setting dial causes simultaneous axial movement of the inner cylinder, where the inner cylinder is rotatably fixed relative the lead screw; anda plunger rod holder rotatably fixed relative to the housing and configured to prevent the plunger rod from rotating during dose setting, where during dose dispensing the plunger rod holder allows the plunger rod to move axially towards the distal end.2. The drive mechanism according to further comprising a cylindrical rotating knob rotatably fixed relative to the dose setting dial.3. The drive mechanism according to further comprising a release knob configured to move axially and distally during dose dispensing to cause the dose setting dial and inner cylinder to simultaneously move distally.4. The drive mechanism according to further characterized in that rotational movement of the plunger rod is prevented by a non-circular ...

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07-01-2016 дата публикации

MEDICAL DEVICE CURVING APPARATUS, SYSTEM, AND METHOD OF USE

Номер: US20160001039A1
Принадлежит:

Apparatus, system, and method for creating a curvature on a medical device during a medical procedure, for example, selecting a curvature from a curve database, customizing the curvature for a specific patient anatomy, and applying the curvature to the medical device during the medical procedure. 1. An apparatus for curving an elongated medical device , the apparatus comprising:a forming unit, having an external surface, positioned adjacent a path along which the elongated medical device is advanced, the forming unit having a support and a heat source;a bending tool, having an external surface, configured to move with respect to the forming unit and to apply a bending force to the elongated medical device such that a distal portion of the elongated medical device is imparted with a permanent curve greater than that on a proximal portion of the elongated medical device; anda barrier positioned to prevent the elongated medical device from contacting the external surface of the forming unit and the external surface of the bending tool, the barrier being configured to permit movement of the bending tool with respect to the forming unit while maintaining sterility of the elongated medical device.2. The apparatus of claim 1 , further comprising a mandrel configured to support the elongated medical device as it is imparted with a permanent curve.3. The apparatus of claim 2 , the mandrel having a composite structure and containing one or more materials configured to be heated by induction.4. (canceled)5. The apparatus of claim 1 , wherein the heat source of the forming unit is configured to produce an inductive field.6. (canceled)7. (canceled)8. (canceled)9. The apparatus of claim 1 , wherein the bending tool is configured to overbend the elongated medical device such that a permanent curve imparted on the elongated medical device is different after the elongated medical device is separated from the apparatus.10. (canceled)11. (canceled)12. (canceled)13. (canceled)14. ( ...

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07-01-2021 дата публикации

MOLD FOR MANUFACTURING PERCUTANEOUS ABSORPTION SHEET, AND APPARATUS AND METHOD FOR MANUFACTURING PERCUTANEOUS ABSORPTION SHEET HAVING NEEDLE-LIKE PROTRUSION

Номер: US20210001102A1
Принадлежит: FUJIFILM Corporation

Provided are a mold for manufacturing a percutaneous absorption sheet that can be detected from an image, and an apparatus and a method for manufacturing a percutaneous absorption sheet having a needle-like protrusion using the mold. The mold is a mold for manufacturing a percutaneous absorption sheet in which a plurality of needle-like recessed portions are disposed, and the problem is solved by a mold for manufacturing a percutaneous absorption sheet in which the mold has a gray color in which a brightness value in a case where a brightness in an HSL (Hue Saturation Lightness) color space is represented in 256 levels is in a range of 30 or more and 200 or less. 1. A mold for manufacturing a percutaneous absorption sheet in which a plurality of needle-like recessed portions are disposed ,wherein the mold has a gray color in which a brightness value in a case where a brightness in an HSL (Hue Saturation Lightness) color space is represented in 256 levels is in a range of 30 or more and 200 or less.2. The mold for manufacturing a percutaneous absorption sheet according to claim 1 ,wherein the mold has a gray color in which the brightness value is in a range of 75 or more.3. The mold for manufacturing a percutaneous absorption sheet according to claim 2 ,wherein the mold has a gray color in which the brightness value is in a range of 150 or less.4. The mold for manufacturing a percutaneous absorption sheet according to claim 1 ,wherein the mold has a gray color in which a saturation value in a case where a saturation in an HSL color space is represented in 256 levels is in a range of 0 or more and 25 or less.5. The mold for manufacturing a percutaneous absorption sheet according to claim 1 ,wherein the mold includes a transparent resin, a white colorant, and a black colorant.6. The mold for manufacturing a percutaneous absorption sheet according to claim 5 ,wherein a mass ratio between the white colorant and the black colorant is 3:1 to 10:1.7. The mold for ...

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04-01-2018 дата публикации

Fluid Atomizer, Nozzle Assembly and Methods for Assembling and Utilizing the Same

Номер: US20180001038A1
Принадлежит: Neogen Corp

A method of assembling a nozzle assembly is disclosed. The method includes: providing a nozzle member having a central passage defined by at least an inner side surface and an inner distal surface; inserting a fluid atomizer into the central passage of the nozzle member; and, with a distal surface of the fluid atomizer arranged adjacent the inner distal surface of the nozzle member, flexing legs of the fluid atomizer in a radially-outward direction for engaging each leg of the legs with the inner side surface of the nozzle member. A fluid atomizer is also disclosed. A nozzle assembly is also disclosed. A method of utilizing a nozzle assembly is also disclosed.

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05-01-2017 дата публикации

DRY POWDER INHALATION DEVICE

Номер: US20170000960A1
Автор: RICHARDSON Eric Carl
Принадлежит: Concentrx Pharmaceuticals, Inc.

Taught herein is a disposable breath actuated dry powder drug inhalation device having a powderized drug storage chamber with integral toroidal geometry and air flow pathways for entraining and breaking up powder aggregates prior to delivery to the patient. The toroidal chamber is fluidly connected by one or more air inlets directed in a non-tangent manner toward the powder to loft and set up an irregular-rotational flow pattern. Also, in fluid connection with the toroidal chamber is a centrally or near centrally located air and powder outlet consisting of one or more holes forming a grid in fluid connection with a channel providing a passageway for powder flow to the patient. 1. An apparatus , comprising:a body having an upper portion and a lower portion, the body defining a toroidal disaggregation chamber, a bottom portion of the toroidal disaggregation chamber being within the lower portion and containing a dry powder drug;a removable partition disposed between the upper portion and the lower portion, the partition retaining the dry powder drug within the bottom portion of the toroidal disaggregation chamber when the upper portion and lower portion are coupled together;an air intake passage configured to place an external volume in fluid communication with the toroidal disaggregation chamber when the partition is removed; andan exit passageway configured to place the external volume in fluid communication with the toroidal disaggregation chamber when the partition is removed such that upon inhalation by the patient on the exit passageway, air is drawn from the air intake passage to the toroidal disaggregation chamber and on to the exit passageway to convey the dry powder drug via the exit passageway to a patient.2. A method of using a single-dose inhalation device to deliver a pre-metered dry powder drug , comprising:removing a protective overwrap packaging from the inhalation device;removing a partition of the inhalation device by pulling an end of the partition ...

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05-01-2017 дата публикации

CUSTOMIZABLE FACIAL SEALING SEGMENT FOR RESPIRATORY DEVICE AND METHOD OF CUSTOMIZING

Номер: US20170000964A1
Автор: SHAFER SANDY JANE
Принадлежит:

A facial sealing segment for a respiratory device includes a sealing flap adapted to sealingly engage the face of a user. The sealing flap is disposed about, and defines, a cutout adapted to receive one or both of the mouth or nares of the user. The facial sealing segment further includes a number of selectively removable portions formed in the sealing flap about the cutout. Each removable portion is defined in the sealing flap by a tear portion. 1. A facial sealing segment for a respiratory device , the sealing segment comprising:a sealing flap adapted to sealingly engage the face of a user, the sealing flap disposed about, and defining a cutout adapted to receive one or both of the mouth or nares of the user; anda number of selectively removable portions formed in the sealing flap about the cutout, each removable portion being defined in the sealing flap by a tear portion.2. The facial sealing segment of claim 1 , wherein the sealing flap comprises a first thickness (t)and wherein the tear portion comprises a localized thickness (t) less than the first thickness.3. The facial sealing segment of claim 1 , wherein the tear portion comprises a groove formed in the sealing flap.4. The facial sealing segment of claim 1 , wherein the groove is formed in a surface of the sealing flap opposite from a surface which sealingly engages the face of the user.5. The facial sealing segment of claim 1 , wherein the tear portion comprises a plurality of perforations formed in the sealing flap.6. The facial sealing segment of claim 1 , wherein the number of removable portions comprise a first portion adapted to be disposed adjacent a first side of the mouth of the user and a second portion adapted to be disposed adjacent a second side of the mouth of the user.7. The facial sealing segment of claim 1 , wherein at least one removable portion of the number of removable portions comprises a pull tab extending from a surface of the sealing flap opposite from a surface which sealingly ...

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05-01-2017 дата публикации

FLUIDIC-CONTROLLED RESERVOIR CANNULA

Номер: US20170000966A1
Принадлежит:

A reservoir cannula is described that has a static fluidic control structure, in that it does not employ a membrane or other moving parts. Furthermore, the reservoir is open to ambient air instead of being sealed. In use, the reservoir cannula enables storage of oxygen and oxygen-rich gas in a storage chamber as well as in and around the patient's nasal passages and nasopharynx, which enables high volume oxygen delivery to the patient early in the next inhalation. Consequently, patients using this delivery mode can carry a smaller and lighter portable oxygen container for ambulatory oxygen, because lower flow oxygen is required to meet their oxygenation needs. In addition, patients requiring a higher flow of oxygen can achieve oxygenation levels previously achieved only by high flow mask or high flow nasal oxygen systems. 1. A cannula for controlling delivery of gas , comprising:an outer shell having an outer surface exposed to ambient air and an inner surface defining a reservoir chamber;an exhaust aperture extending through the outer shell to the reservoir chamber and having an open surface area dimension;a static structure disposed within the reservoir chamber and including a fluidic controller having a nasal port; anda nasal prong fitted to the nasal port and extending through the exhaust aperture, wherein the nasal prong has an outer area dimension which is less than the open surface area dimension of the exhaust aperture to permit gas to escape from the cannula.2. The cannula of claim 1 , wherein the fluidic controller further includes a supply port and a collection port.3. The cannula of claim 2 , wherein the fluidic controller controls delivery of gas from the reservoir chamber and the supply port in response to a breathing cycle.4. The cannula of claim 2 , wherein the collection port is in communication with the reservoir chamber.5. The cannula of claim 4 , further comprising a collection tube having a proximal end fitted to the collection port and a distal ...

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05-01-2017 дата публикации

COMPONENTS FOR MEDICAL CIRCUITS

Номер: US20170000967A1
Принадлежит:

Condensation or “rain-out” is a problem in medical circuits and previous attempts to manage and/or prevent rain-out have resulted in relatively expensive and/or difficult to manufacture medical circuit components. The subject patent provides an improved medical circuit component for managing rain-out. In particular the component may be an improved breathing tube, or insufflation system limb comprising a helically corrugated tube preferably incorporating a heater wire. 1a helically corrugated tube wherein the corrugation profile comprises alternating outer crests and inner troughs,a heater wire associated with said outer crests.. A component comprising: This application is a continuation of U.S. application Ser. No. 13/805640, filed Mar. 8, 2013, which, is the U.S. National Phase application under 35 U.S.C. §371 of International Application No. PCT/NZ2011/000111, filed Jun. 16, 2011, which claims priority from U.S. Provisional Application No. 61/357333, filed Jun. 22, 2010. The entirety of each of the foregoing applications is incorporated herein by reference.Field of the InventionThe present invention relates to components for medical circuits for conveying gases to and/or from a patient. In one particular aspect, the invention relates to conduits and in particular to heated breathing tubes for use in an inspiratory and/or expiratory limb of a breathing circuit. In another particular aspect the invention relates to a heated tube for a surgical insufflation system.Description of the Related ArtIn assisted breathing, particularly in, medical applications, gases having high levels of relative humidity are supplied and returned through flexible breathing tubes of a relatively restricted size typically between a range of approximately 10 mm to 25 mm diameter (covering both neonatal and adult applications). Such breathing tubes are ideally very light, resistant to kinking or pinching but also very flexible to ensure the greatest performance and level of comfort for the ...

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05-01-2017 дата публикации

METHODS FOR MANUFACTURING A GUIDE WIRE UTILIZING A COLD WORKED NICKEL-TITANIUM-NIOBIUM TERNARY ALLOY

Номер: US20170000985A1
Принадлежит:

Guide wire devices fabricated from a linear pseudo-elastic Ni—Ti alloy and methods for their manufacture. The Ni—Ti alloy that includes nickel, titanium, and about 3 atomic % (at %) to about 30 at % niobium (Nb). Cold working the Ni—Ti alloy stabilizes the alloy's martensitic phase and yields a linear pseudo-elastic microstructure where reversion to the austenite phase is retarded or altogether blocked. The martensitic phase of cold worked, linear pseudo-elastic Ni—Ti—Nb alloy has an elastic modulus that is considerably higher than the comparable cold worked, linear pseudoelastic binary Ni—Ti alloy. This yields a guide wire device that has better torque response and steerability as compared to cold worked, linear pseudoelastic binary Ni—Ti alloy or superelastic binary Ni—Ti alloy. 1. A method for fabricating a guide wire device , comprising:providing an elongated shaft member that includes a proximal section and a distal section, wherein at least a portion of the elongated shaft member comprises a nickel-titanium (Ni—Ti) alloy comprising nickel (Ni), titanium (Ti), and niobium (Nb); andcold working at least the Ni—Ti alloy to yield a Ni—Ti alloy that exhibits linear pseudoelastic behavior and that displays a martensitic phase.2. The method of claim 1 , wherein the Ni—Ti alloy comprises about 3 at % Nb to about 30 at % Nb and Ni is present in an amount about 2 at % to about 4 at % higher than an at % of Ti.3. The method of claim 2 , wherein Ni is present in an amount about 3 at % higher than an at % of Ti.4. The method of claim 3 , wherein the Ni—Ti alloy comprises about 47 at % Ni claim 3 , about 44 at % Ti claim 3 , and about 9 at % Nb.5. The method of claim 1 , wherein providing the elongated shaft member includes fabricating the elongated shaft member by at least one of drawing or grinding.6. The method of claim 1 , wherein the cold working includes at least one of high force flattening claim 1 , drawing claim 1 , stamping claim 1 , rolling claim 1 , or swaging.7 ...

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05-01-2017 дата публикации

Brain Portal

Номер: US20170000996A1
Автор: alan edward odonnell
Принадлежит: Individual

The Brain Portal is a device that allows for easy access to the brain for treatments that require multiple visits inside the brain case to alleviate the need for multiple craniotomies. Such treatments could involve multiple injections of medicines that have to be given over a period of days or weeks. In a different configuration, it also allows for electrical stimulation of the brain thru electrodes without the need for batteries, and allows the flow of electricity from outside the brain to the affected areas using induction coils. The Brain Portal can also be used as an easy means to collect samples of cerebral spinal fluid without the need of a spinal tap. Furthermore, having an easy access allows the physician the option of injecting drugs directly into the brain, bypassing the blood-brain barrier, thereby lowering the dosage needed to treat disease.

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02-01-2020 дата публикации

Cap assembly for a drug delivery device, kit for assembling a cap, method for assembling a cap and drug delivery device comprising a cap assembly

Номер: US20200001020A1
Автор: Plumptre David Aubrey
Принадлежит:

A multi-part cap assembly for a drug delivery device is provided, the cap assembly comprising: a first cap component, and a second cap component, wherein the first cap component is assembled to the second cap component, wherein one of the first cap component and the second cap component is provided with a guide track and the other one of the first cap component and the second cap component is provided with a guide feature, wherein the guide track and the guide feature are arranged to cooperate to form an axial guiding interface between the first cap component and the second cap component, and wherein the axial guiding interface is configured such that relative rotational movement between the first cap component and the second cap component is restricted or prevented. Furthermore, a kit for assembling a cap and a method for assembling a cap are provided as well as a drug delivery device. 1. A multi-part cap assembly for a drug delivery device , comprising:a first cap component; anda second cap component, whereinthe first cap component is assembled to the second cap component, wherein one of the first cap component and the second cap component is provided with a guide track and the other one of the first cap component and the second cap component is provided with a guide feature, wherein the guide track and the guide feature are arranged to cooperate to form an axial guiding interface between the first cap component and the second cap component, and wherein the axial guiding interface is configured such that relative rotational movement between the first cap component and the second cap component is restricted or prevented.2. The cap assembly of claim 1 ,wherein the first cap component and the second cap component are configured such that, aside from the guiding interface, the relative angular orientations of the first cap component and the second cap component, in which the first cap component can be assembled to the second cap component are limited, wherein the ...

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02-01-2020 дата публикации

Systems and methods for evaluation of electrophysiology systems

Номер: US20200001036A1
Принадлежит: Biosig Technologies Inc

A signal processing evaluator and methods that compare a digital waveform of a cardiac signal to a first processed signal generated by a test system such as an EP recorder or an EP mapping system and generates a first finding evaluating how well the test system filters non-cardiac signals or simulated body impedance. A simulator and methods that send cardiac signals including non-cardiac signals or simulated body impedance to a test system and to a signal processing evaluator for evaluation of the test system.

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03-01-2019 дата публикации

Container for Closing Caps for Syringes

Номер: US20190001049A1
Принадлежит: HEALTH ROBOTICS S.R.L.

A container for closing caps for syringes has a plurality of seats, each of which is suited to be engaged, in a sliding manner, by a respective closing cap, and has a movable portion configured to move between a locking position of the relevant closing cap in the seat and a release position. 123133521335203821335. A container for closing caps () for syringes () , the container comprising a plurality of seats (; ) , which are suited to be each engaged , in a sliding manner , by a respective closing cap (); wherein each seat (; ) has a movable portion (; ) , which is configured to move between a locking position , in which it locks the relevant closing cap () in the seat (; ) , and a release position.22021316213. Container claim 1 , according to claim 1 , wherein the movable portion () is arranged so as to lock the closing cap () in the seat () parallel to a direction () in which the closing cap () is inserted/extracted into/from the seat ().3201621320132013. Container claim 1 , according to claim 1 , wherein the movable portion () moves transversely to a direction () in which the closing cap () is inserted/extracted into/from the seat () between its locking position claim 1 , wherein the movable portion () defines a closing cap of the seat () claim 1 , and its release position claim 1 , in which the mobile portion () is arranged outside of the seat ().413192019. Container claim 1 , according to claim 1 , wherein the seats () are aligned with one another in an alignment direction (); each movable portion () comprising a movable tooth claim 1 , which moves in the alignment direction () between said locking and release positions.51813191819. Container claim 4 , according to claim 4 , and comprising claim 4 , furthermore claim 4 , a guide rod () claim 4 , which extends on the outside of the seats () and is movable in the alignment direction (); each tooth projecting from the guide rod () transversely to the alignment direction ().613. Container claim 5 , according to ...

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03-01-2019 дата публикации

SURFACE HARDENED INJECTION NEEDLE AND METHOD OF PRODUCING SUCH

Номер: US20190001073A1
Принадлежит:

A medical injection needle () having a metallic needle body () comprising an axially extending wall (), a first end portion (), a second end portion (), and a flow path () providing for fluid communication between the first end portion () and the second end portion () along the axially extending wall (), wherein at least a portion of the metallic needle body () comprises a hardened surface layer () in which carbon atoms and nitrogen atoms are deposited. 2. A medical injection needle according to claim 1 , wherein the hardened surface layer has a radial extent (r claim 1 , r) which does not exceed 25 μm.3. A medical injection needle according to claim 1 , wherein the hardened surface layer has a radial extent (r claim 1 , r) which does not exceed 10 μm.4. A medical injection needle according to claim 1 , wherein the hardened surface layer comprises an inner layer in which predominantly carbon atoms are deposited and an outer layer in which predominantly nitrogen atoms are deposited.5. A medical injection needle according to claim 1 , wherein the at least a portion of the metallic needle body comprises the first end portion.6. A medical injection needle according to claim 1 , wherein the first end portion comprises a sharpened tip.7. A medical injection needle according to claim 1 , wherein the metallic needle body comprises a radially outwardly oriented surface and a radially inwardly oriented surface claim 1 , andwherein the hardened surface layer is present along at least a portion of at least one of the radially outwardly oriented surface and the radially inwardly oriented surface.8. A medical injection needle according to claim 7 , wherein the axially extending wall is tubular and has a thickness (t) in the range 25 μm to 50 μm.9. A medical injection needle according to claim 7 , wherein a first hardened surface layer is present along at least a portion of the radially outwardly oriented surface and a second hardened surface layer is present along at least a ...

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03-01-2019 дата публикации

MICROSTRUCTURE FOR TRANSDERMAL ABSORPTION AND METHOD FOR MANUFACTURING SAME

Номер: US20190001109A1
Принадлежит:

The present invention relates to a microstructure including a biocompatible polymer or an adhesive and to a method for manufacturing the same. The present inventors optimized the aspect ratio according to the type of each microstructure, thereby ensuring the optimal tip angle and the diameter range for skin penetration. Especially, the B-type to D-type microstructures of the present invention minimize the penetration resistance due to skin elasticity at the time of skin attachment, thereby increasing the penetration rate of the structures (60% or higher) and the absorption rate of useful ingredients into the skin. In addition, the D-type microstructure of the present invention maximizes the mechanical strength of the structure by applying a triple structure, and thus can easily penetrate the skin. When the plurality of microstructures are arranged in a hexagonal arrangement type, a uniform pressure can be transmitted to the whole microstructures on the skin. 1. A microstructure comprising a biocompatible polymer or an adhesive , wherein the aspect ratio (w:h) , configured of the diameter (w) of the bottom surface of the microstructure and the height (h) of the microstructure , is 1:5 to 1:1.5 , and the angle of a distal tip is 10° to 40°.2. The microstructure of claim 1 , wherein the biocompatible polymer is at least one polymer selected from the group consisting of hyaluronic acid (HA) claim 1 , carboxymethyl cellulose (CMC) claim 1 , alginic acid claim 1 , pectin claim 1 , carrageenan claim 1 , chondroitin (sulfate) claim 1 , dextran (sulfate) claim 1 , chitosan claim 1 , polylysine claim 1 , collagen claim 1 , gelatin claim 1 , carboxymethyl chitin claim 1 , fibrin claim 1 , agarose claim 1 , pullulan polylactide claim 1 , polyglycolide (PGA) claim 1 , polylactide-glycolide copolymer (PLGA) claim 1 , pullulan polyanhydride claim 1 , polyorthoester claim 1 , polyetherester claim 1 , polycaprolactone claim 1 , polyesteramide claim 1 , poly(butyric acid) claim 1 , ...

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03-01-2019 дата публикации

Medical connectors and methods of use

Номер: US20190001114A1
Автор: Thomas F. Fangrow
Принадлежит: ICU Medical Inc

Some embodiments disclosed herein relate to a medical connector with an internal cavity with an internal closure system having a dome valve configured to resist retrograde fluid flow caused by various sources, including patient activity and fluid administration activity. A proximal closure system with a seal member and a moveable plug are also located within the internal cavity.

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05-01-2017 дата публикации

WORKPIECE CARRIER FOR TRANSPORTING AND/OR STORING COMPONENTS OF DRUG DELIVERY DEVICES

Номер: US20170001757A1
Принадлежит:

The present invention relates to a workpiece carrier for transporting and/or storing components of a drug delivery device, comprising: an array of accommodating recesses extending in a first lateral plane (x, y) and being adapted to receive at least one component of the drug delivery device, at least one stack forming structure adapted to mate with a corresponding stack forming structure of another workpiece carrier for mutually aligning workpiece carriers when stacked on one another, wherein the center of the at least one stack forming structure is arranged laterally offset with respect to the center of the array of accommodating recesses in at least one lateral direction, and wherein the stack forming structure comprises a surrounding edge comprising at least in sections a corrugated or undulated structure. 1. A workpiece carrier for transporting and/or storing components of a drug delivery device , comprising:an array of accommodating recesses extending in a first lateral plane (x, y) and being adapted to receive at least one component of the drug delivery device,at least one stack forming structure formed to mate with a corresponding stack forming structure of another workpiece carrier for mutually aligning workpiece carriers when stacked on one another,wherein the center of the at least one stack forming structure is arranged laterally offset with respect to the center of the array of accommodating recesses in at least one lateral direction (x, y) lying in the first lateral plane, andwherein the stack forming structure comprises a surrounding edge comprising at least in sections a corrugated or undulated structure; andwherein the stack forming structure comprises at least one outwardly extending projection having an inward directed ledge at its lower end formed to abut against a flange portion of another workpiece carrier stacked beneath in a first orientation.2. The workpiece carrier according to claim 1 , wherein the stack forming structure is adapted to ...

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13-01-2022 дата публикации

Gastric retentive devices

Номер: US20220008334A1
Принадлежит: Clexio Bioscience Ltd

Provided are devices that are configured for gastric retention for a period of at least six hours (or at least three hours if the subject is in the fasted state) while maintaining their structural integrity and releasing or holding an active or diagnostic agent into or in gastric fluid of a human subject over that period, as well as methods of delivering an agent over an extended period by orally administering such devices to a subject, uses of an enteric polymer in the formation of devices that deliver an agent over an extended period of time, and methods of making such devices.

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13-01-2022 дата публикации

Methods for generating and delivering droplets to the pulmonary system using a droplet delivery device

Номер: US20220008669A1
Принадлежит: Pneuma Respiratory Inc

A droplet delivery device and related methods for delivering precise and repeatable dosages to a subject for pulmonary use is disclosed. The droplet delivery device includes a housing, a reservoir, and ejector mechanism, and at least one differential pressure sensor. The droplet delivery device is automatically breath actuated by the user when the differential pressure sensor senses a predetermined pressure change within housing. The droplet delivery device is then actuated to generate a stream of droplets having an average ejected droplet diameter within the respirable size range, e.g, less than about 5 μm, so as to target the pulmonary system of the user.

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01-01-2015 дата публикации

IMPLANTABLE DEVICES AND METHODS FOR EVALUATION OF ACTIVE AGENTS

Номер: US20150005595A1
Принадлежит:

Devices for the local delivery of microdose amounts of one or more active agents, alone or in combination, in one or more dosages, to selected tissue of a patient are described. The devices generally include multiple microwells arranged on or within a support structure and contain one or more active agents, alone or in combination, in one or more dosages and/or release pharmacokinetics. In an exemplary embodiment, the device has a cylindrical shape, having symmetrical wells on the outside of the device, each well containing one or more drugs, at one or more concentrations, sized to permit placement using a catheter, cannula, or stylet. Optionally, the device has a guidewire, and fiber optics, sensors and/or interactive features such as remote accessibility to provide for in situ retrieval of information and modification of device release properties. In a preferred embodiment, the fiber optics and/or sensors are individually accessible to discrete wells. 1. An implantable microdevice comprising:a support structure having microwells on a surface of or formed within the support structure; optionally including a compound release mechanism for controlling the release of an active agent from the microwells;wherein the device is configured to permit implantation into a tissue using a catheter, cannula or biopsy needle, andwherein the device is further configured to release one or more active agents from the microwells to separate and discrete areas of tissue adjacent to the microwell.2. The microdevice of claim 1 , comprising an active agent release mechanism selected from the group consisting of the dimensions of an opening into the microwells claim 1 , a film claim 1 , a membrane claim 1 , a polymer matrix claim 1 , and a hydrogel pad.3. The microdevice of further comprising one or more active agent or combinations of active agent within the microwells.4. The microdevice of wherein the active agent or combinations thereof are present in different amounts.5. The ...

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20-01-2022 дата публикации

PRIMARY CONTAINERS WITH IMPROVED PROTEIN DRUG STABILITY AND LOWER IMMUNE RESPONSE

Номер: US20220016348A1
Принадлежит:

A primary drug container is described having an injection-molded thermoplastic wall having an internal surface defining a lumen, a PECVD (plasma-enhanced chemical vapor deposition) drug-contact coating, and a polypeptide composition contained in the lumen. The drug-contact coating is on or adjacent to the internal surface, positioned to contact a fluid in the lumen, and consists essentially of SiOxCyHz. The primary drug container contains between a lower limit of 1,000 and an upper limit of 100,000 particles having effective spherical diameters greater than 2 and no more than 10 micrometers (μm) per mL of solution. 1. A primary drug container comprising:a wall having an internal surface defining a lumen; and{'sub': x', 'y', 'z, 'claim-text': x is between 0.5 and 2.4 as measured by x-ray photoelectron spectroscopy (XPS),', 'y is between 0.6 and 3 as measured by XPS; and', 'z is between 2 and 9 as measured by Rutherford backscattering; and, 'a PECVD drug-contact coating on or adjacent to the internal surface and positioned to contact a fluid in the lumen, in which the drug-contact coating consists essentially of SiOCH, in which'}a polypeptide composition contained in the lumen in contact with the PECVD drug-contact coating;the primary drug container containing between a lower limit of 1,000, alternatively 2,000, alternatively 3,000, and an upper limit of 100,000, alternatively 75,000, alternatively 50,000, alternatively 25,000, alternatively 20,000, alternatively 18,000, alternatively 16,000, alternatively 14,000, alternatively 12,000, alternatively 10,000, alternatively 8,000, alternatively 6,000, alternatively 4,000, alternatively 3,000 particles having effective spherical diameters greater than 2 and no more than 10 micrometers (μm) per mL of solution;in which the particle count is measured by filling the primary drug container with 1 mg/mL IVIg in 250 mM glycine pH 4.25 with 0.02% (v/v) PS20 and rotating the primary container end-over end at room temperature for ...

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20-01-2022 дата публикации

AUTOINJECTOR AND METHOD OF ASSEMBLING

Номер: US20220016358A1
Принадлежит:

The disclosure further relates to an autoinjector and a method of assembling the autoinjector. A syringe carrier is disclosed comprising a housing adapted to receive a syringe. They syringe includes a needle encapsulated by a removable protective needle sheath. The syringe carrier further includes two or more flexible arms protruding outwards in a relaxed state and adapted to couple with the syringe in a mounted position. In the mounted position, the flexible arms deflect radially inwards due, in part, to an axial force operating on the syringe carrier. 115-. (canceled)16. An autoinjector comprising: a housing adapted to receive a syringe having a needle encapsulated by a distal removable protective needle sheath, and', 'two or more flexible arms adapted to couple with the syringe in a mounted position; and', 'a case adapted to receive the syringe carrier., 'a syringe carrier comprising'}17. The autoinjector according to claim 16 , wherein the two or more flexible arms are configured to deflect inwardly claim 16 , and an inward deflection of the two or more flexible arms is provided by a control feature arranged on the case.18. The autoinjector according to claim 16 , wherein the flexible arms extend distally from a front end of the syringe carrier.19. The autoinjector according to claim 16 , wherein the two or more flexible arms comprise protrusions inwardly directed and configured to couple with a distal shoulder of the syringe.20. The autoinjector according to claim 19 , wherein an inner diameter of the protrusions is smaller than an outer diameter of the protective needle sheath and an outer diameter of a shaft of the syringe.21. The autoinjector according to claim 16 , wherein the housing includes a proximal aperture having an outer diameter claim 16 , in part claim 16 , smaller than an outer diameter of a proximal syringe flange of the syringe.22. The autoinjector according to claim 16 , wherein the case is adapted to inwardly deflect the two or more flexible ...

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20-01-2022 дата публикации

BALLOON DILATION CATHETER, BALLOON AND PREPARATION METHOD THEREFOR

Номер: US20220016400A1
Принадлежит:

A balloon dilation catheter, a balloon () and preparation method therefor. The balloon () is prepared by co-mixing at least two of L25, TR55, TR90, and TR70, and has high puncture resistance and low compliance with respect to a balloon () made of a single nylon material. The balloon () is preferably a hollow multilayer structure, and the puncture resistance of the balloon () can be further improved and the compliance can be further reduced with respect to a single-layer structure. 1. A balloon , wherein the balloon is made of a blend of at least two selected from the group consisting of L25 , TR55 , TR90 and TR70.2. The balloon according to claim 1 , wherein the balloon is made of a blend of L25 and TR55 claim 1 , or a blend of L25 and TR90 claim 1 , or a blend of L25 claim 1 , TR55 and TR90 claim 1 , or a blend of L25 and TR70.3. The balloon according to claim 1 , wherein the balloon is made of a blend of L25 and TR55 with a weight ratio of L25 to TR55 ranging from 9:1 to 7:3; orthe balloon is made of a blend of L25 and TR90 with a weight ratio of L25 to TR90 ranging from 9:1 to 6:4; orthe balloon is made of a blend of L25, TR55 and TR90, wherein the TR90 is present at a weight percentage of 10% and a weight ratio of L25 to TR55 ranges from 7:2 to 5:4; orthe balloon is made of a blend of L25 and TR70 with a weight ratio of L25 to TR70 ranging from 9:1 to 7:3.4. The balloon according to claim 1 , wherein the balloon is made of a blend of L25 and TR55 with a weight ratio of L25 to TR55 of 8:2; orthe balloon is made of a blend of L25 and TR90 with a weight ratio of L25 to TR90 of 7:3 or 8:2; orthe balloon is made of a blend of L25, TR55 and TR90 with an L25:TR55:TR90 weight ratio of 6:3:1; orthe balloon is made of a blend of L25 and TR70 with a weight ratio of L25 to TR70 of 9:1.5. The balloon according to claim 1 , wherein the balloon has a hollow multi-layer structure consisting of radially stacked layers of the same thickness and material.6. The balloon according ...

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12-01-2017 дата публикации

POROUS ACUPUNCTURE NEEDLE AND METHOD FOR MANUFACTURING SAME

Номер: US20170007499A1

The present invention relates to a porous acupuncture needle and a method for manufacturing the same and, more specifically, to a porous acupuncture needle, which has mirco-sized or nano-sized holes formed on the surface thereof to maximize the specific surface thereof, and a method for manufacturing the same. 1. A porous acupuncture needle , comprising 5 to 20 holes per 100 μmsurface area.2. The porous acupuncture needle of claim 1 , wherein the hole has an average diameter in a range of 0.05 to 3 μm.3. The porous acupuncture needle of claim 1 , wherein the hole has an average depth in a range of 1 to 3 μm.4. The porous acupuncture needle of claim 1 , wherein the hole is loaded with a drug.5. The porous acupuncture needle of claim 1 , wherein when a specific surface area is measured according to a method in which a specific surface area is calculated after measuring an amount of a methylene blue solution stained at a surface of an acupuncture needle claim 1 , the specific surface area is in a range of 0.0150 to 0.0350 m/g.6. The porous acupuncture needle of claim 5 , comprising iron (Fe) at 45 to 46% claim 5 , chromium (Cr) at 17 to 19% claim 5 , carbon (C) at 30 to 34% claim 5 , nickel (Ni) at 2 to 3% and aluminum (Al) at 1.5 to 2% claim 5 , when measured by an energy dispersive spectrometer (EDS). (original) A method of preparing a porous acupuncture needle claim 5 , comprising forming a porous structure at a surface of the needle by performing an anodizing process.87. The method of claim claim 5 , wherein the anodizing process is performed in an electrolyte containing the needle and a carbon electrode claim 5 , the needle is used as a positive electrode and the carbon electrode is used as a negative electrode claim 5 , and the anodizing process is performed by applying a direct current voltage of 20 to 38V for 30 minutes to 2 hours.9. The method of claim 8 , wherein the electrolyte includes one or more selected from an ethylene glycol aqueous solution and a ...

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12-01-2017 дата публикации

INTEGRATED MEDICAL PUMP AND OXYGENATOR

Номер: US20170007755A1
Принадлежит:

Extracorporeal circuit devices that can be used for on-pump open-heart surgery to support surgical procedures such as coronary artery bypass grafting are described. In some embodiments, an oxygenator can include an integral pump. Such an integrated arrangement can advantageously provide an extracorporeal circuit with a lower overall volume than other conventional extracorporeal circuits. 1. A blood oxygenator apparatus comprising:an outer housing;a heat exchanger disposed within the outer housing, the heat exchanger defining an internal space;an oxygenator disposed within the outer housing, the oxygenator arranged concentrically around the heat exchanger; anda pump assembly disposed concentrically within the internal space, the pump assembly comprising a rotary vane member that is rotatable in relation to the heat exchanger and the outer housing, the rotary vane member defining a maximum diameter, the rotary vane member defining an axial length,wherein the axial length of the rotary vane member is greater than the maximum diameter of the rotary vane member.2. The blood oxygenator apparatus of claim 1 , wherein the pump assembly is selectively coupleable with the outer housing.3. The blood oxygenator apparatus of claim 1 , wherein a ratio of the axial length of the rotary vane member to the maximum diameter of the rotary vane member is greater than or equal to about 2:1.5.4. The blood oxygenator apparatus of claim 1 , further comprising a flow distribution element disposed within the internal space.5. The blood oxygenator apparatus of claim 4 , wherein the flow distribution element is configured to facilitate a substantially uniform radial flow rate of blood entering the heat exchanger.6. A blood oxygenator apparatus comprising:a heat exchanger defining an internal space; andan oxygenator arranged concentrically around the heat exchanger,wherein the heat exchanger and the oxygenator are disposed within a housing, wherein the housing is configured to be selectively ...

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12-01-2017 дата публикации

DOSE COUNTERS FOR INHALERS, INHALERS AND METHODS OF ASSEMBLY THEREOF

Номер: US20170007785A1
Принадлежит:

A tape system for a dose counter for an inhaler, the tape system having a main elongate tape structure, dosing indicia located on the main elongate tape structure, tape positioning indicia located on the main elongate tape structure, a tape size marker located on the main elongate tape structure indicating a number of dosing indicia on the tape, and priming indicia located on the main elongate tape structure, the priming indicia being located between the dosing indicia and one end of the tape. 1. A tape system for a dose counter for an inhaler , the tape system having a main elongate tape structure , dosing indicia located on the main elongate tape structure , tape positioning indicia located on the main elongate tape structure , a tape size marker located on the main elongate tape structure indicating a number of dosing indicia on the tape , and priming indicia located on the main elongate tape structure , the priming indicia being located between the dosing indicia and one end of the tape.2. The tape system of claim 1 , wherein the dosing indicia comprise numbers printed on the tape.3. The tape system of claim 1 , wherein the priming indicia is a priming dot located on the tape structure that is to be aligned with a window on the inhaler that is visible to a user of the inhaler.4. The tape system of claim 1 , wherein the tape positioning indicia comprise a series of lines that are each formed across the tape.5. The tape system of claim 1 , wherein the tape size marker is positioned between said one end of the tape and the tape positioning indicia.6. The tape system of claim 1 , wherein the tape positioning indicia are positioned between said one end of the tape and the dosing indicia.7. The tape system of claim 1 , wherein said one end of the tape is fixed to a tape reel shaft.8. The tape system of claim 1 , wherein the priming indicia is positioned between the dosing indicia and the tape positioning indicia.9. The tape system of claim 1 , wherein the tape size ...

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12-01-2017 дата публикации

Actuator and Nose Piece for a Nasal Inhaler

Номер: US20170007788A1
Автор: Brewer Richard D
Принадлежит:

The present invention provides an actuator () for a nasal inhaler (). The actuator comprises an elongate body () comprising a canister opening (), a nose piece () adapted for nasal delivery of a medicament, and fixing means for fixing the nose piece to the elongate body (). The nose piece is fixable to the body at an acute angle to the elongate body. A first portion of the nose piece defines an outlet () for discharging a medicament from the actuator. The nose piece is adapted and the elongate body is adapted so that when the nose piece is fixed to the elongate body, the nose piece and elongate body cooperate to define a fluid communication pathway from the canister opening to the outlet. The present invention is also directed to an inhaler comprising an actuator as discussed, and a canister. 1. An actuator for a nasal inhaler , the actuator comprising an elongate body comprising a canister opening for insertion of a canister for supplying a medicament ,a nose piece adapted for nasal delivery of the medicament, the nose piece being fixable to the body at an acute angle to the elongate body, a first portion of the nose piece defining an outlet for discharging a medicament from the actuator, andfixing means for fixing the nose piece to the body,wherein the nose piece is adapted and the body is adapted so that when the nose piece is fixed to the body the nose piece and body cooperate to define a fluid communication pathway from the canister opening to the outlet.2. An actuator as claimed in claim 1 , further comprising a second portion of the nose piece defining an orifice through which medicament may pass from the body to the nose piece.3. An actuator as claimed in either or claim 1 , wherein the canister has a valve stem and wherein the actuator further comprises a stem socket adapted for receiving the valve stem of the canister.4. An actuator as claimed in claim 3 , wherein the stem socket is comprised in a stem post.5. An actuator as claimed in any one of to claim ...

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12-01-2017 дата публикации

HOUSINGS FOR USE WITH INFLATION DEVICES AND RELATED METHODS

Номер: US20170007806A1
Принадлежит:

A housing for use in connection with an inflation device can be coupled to a syringe body by a snap-fit connection. The snap-fit type mechanism can include an adaptor and a lock, such as a depressible lock. The housing can enclose an electrical circuit and a display screen that rests on a plurality of resilient pins. The circuit board may be held in place within the housing via one or more heat pins. The inflation device can be configured to measure pressure within a fluid reservoir of a syringe. 1. A syringe assembly comprising:an elongate syringe barrel defining a fluid reservoir;a housing that is coupled to the elongate syringe barrel via a snap-fit connection;a pressure transducer; andan aperture that extends through a wall of the elongate syringe barrel such that the fluid reservoir of the elongate syringe barrel is in fluid communication with the pressure transducer; an adaptor that is coupled to the elongate syringe barrel, the adaptor comprising a plurality of flanges, wherein each flange of the plurality of flanges is in contact with the housing; and', 'a lock that is coupled to the housing, the lock preventing movement of the adaptor relative to the housing., 'wherein the snap-fit connection comprises2. The syringe assembly of claim 1 , further comprising a circuit board and a display screen claim 1 , wherein the circuit board and the display screen are each disposed within the housing.3. The syringe assembly of claim 2 , wherein the pressure transducer is disposed between the adaptor and the lock.4. The syringe assembly of claim 3 , wherein the pressure transducer claim 3 , circuit board claim 3 , and display screen are configured for electrical communication with one another.5. The syringe assembly of claim 1 , wherein the lock is configured to engage with the adaptor to prevent movement of the adaptor relative to the housing after the lock has been depressed.6. The syringe assembly of claim 1 , wherein the lock comprises a first portion for coupling to ...

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12-01-2017 дата публикации

DILATOR AND METHOD FOR PENILE PROSTHETIC IMPLANTATION

Номер: US20170007809A1
Автор: Daniel Geoffrey A.
Принадлежит:

A dilator configured for dilating tissue of a corpora cavernosum of a penis having a dilation body defined along a longitudinal axis of the dilator and an extendable wing connected to the dilation body. A knob is provided at a first proximal end portion of the dilation body and is configured to communicate with the extendable wing. Rotating the knob extends the extendable wing away from the dilation body and changes an effective diameter of the dilator. Also disclosed is a method of dilating the corpora cavernosum of a penis and a method of implanting a penile prosthetic in the corpora cavernosum of a penis. 1. A dilator configured for dilating tissue of a corpora cavernosum of a penis , comprising:a dilation body defined along a longitudinal axis of the dilator;an extendable wing connected to the dilation body;wherein a knob is provided at a first proximal end portion of the dilation body and configured to communicate with the extendable wing.2. The dilator according to claim 1 , wherein claim 1 , in a first claim 1 , closed state of the dilator claim 1 , a first external surface of the extendable wing is configured to be flush with a second external surface of the dilation body.3. The dilator according to claim 1 , wherein the extendable wing is connected to the dilation body in one or more hinge points configured along the dilation body.4. The dilator according to claim 1 , wherein the extendable wing is connected to the dilation body along a turn rod provided in the dilation body.5. The dilator according to claim 1 , wherein the extendable wing is operable to increase an effective diameter of the dilator up to two times.6. The dilator according to claim 1 , wherein the extendable wing comprises a tip portion including a blade.7. The dilator according to claim 6 , wherein the blade is configured to skive tissue within the corpora cavernosum when the dilation body is rotated.8. The dilator according to claim 1 , wherein the extendable wing comprises a tip portion ...

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12-01-2017 дата публикации

TATTOOING SYSTEMS AND METHODS

Номер: US20170007814A1
Принадлежит: ELWHA LLC

A tattooing apparatus including a needle having at least one tip. The needle is configured to move between a first position in which the tip is located above the surface of a skin, and a second position in which the tip is located at a penetration depth underneath the skin surface. The needle is further configured to deposit an ink between the skin surface and the penetration depth. The tattooing apparatus further includes a needle drive mechanism configured to move the needle between the first position and the second position. The tattooing apparatus includes a sensor configured to output a feedback signal corresponding to a skin thickness characteristic. The tattooing apparatus further includes a controller configured to receive the feedback signal, wherein the controller is configured to adjust the penetration depth based on the skin thickness characteristic. 1. A method of tattooing comprising:configuring a tattooing system with a setting corresponding to a layer of skin where an ink is to be deposited;causing a needle to oscillate in and out of a skin at a penetration depth such that the needle deposits the ink into the layer of skin;causing an adjustment to the penetration depth in response to a feedback signal from a sensor indicating a detected change in depth of the layer of skin from a surface of the skin such that the needle continues to deposit the ink into the layer of skin.2. The method of claim 1 , wherein the setting includes a depth percentage within the layer of skin where the ink is to be deposited.3. The method of claim 2 , further comprising causing the adjustment to the penetration depth in response to a detected change in a thickness of the layer of skin such that the needle continues to deposit the ink at the depth percentage within the layer of skin.4. The method of claim 1 , wherein the setting includes a depth within the layer of skin where the ink is to be deposited.5. The method of claim 1 , wherein the layer of skin is an epidermis ...

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14-01-2016 дата публикации

CATHETER ADD-ON AND METHODS OF PRODUCING AND USING SAME

Номер: US20160008570A1
Принадлежит: ANDROPHIN MEDICAL LTD.

An apparatus comprising: (a) a main body adapted to engage and retain a catheter therein at a fixed point relative to the catheter length; and (b) a cutting mechanism adapted to sever said catheter in response to a pre-defined threshold force applied along the length of the catheter. 1. An apparatus comprising:(a) a main body adapted to engage and retain a catheter therein at a fixed point relative to the catheter length; and(b) a cutting mechanism adapted to sever said catheter in response to a pre-defined threshold force applied along the length of the catheter.23-. (canceled)4. An apparatus according to claim 1 , wherein said cutting mechanism employs a fixed blade.5. An apparatus according to claim 4 , comprising a pair of arms with an aperture between them positioned between said fixed blade and a catheter engaged and retained in said main body.6. An apparatus according to claim 5 , comprising a blade holder designed and configured to hold said blade in a fixed orientation with respect to said arms and with respect to said main body.7. An apparatus according to claim 5 , wherein said pair of arms are integrally formed with or attached to a portion of said main body claim 5 , and comprising a blade holder designed and configured for insertion in a corresponding socket in said main body.8. An apparatus according to claim 4 , wherein said fixed blade is embedded within a resilient material.9. (canceled)10. An apparatus according to wherein said fixed blade is separated from said catheter by a break-away pin when said catheter is engaged and retained by said main body.11. An apparatus according to claim 1 , wherein said cutting mechanism includes one or more blades which move in response to application of the threshold force.1213-. (canceled)14. An apparatus according to claim 1 , comprising a tensioning collar adapted to restrict axial translation of said main body with respect to a catheter retained therein.15. A method comprising:(a) fashioning a main body ...

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14-01-2016 дата публикации

PERCUTANEOUS PORT GUARD DRESSING

Номер: US20160008576A1
Автор: LEE Sang Beom, SMITH Kevin
Принадлежит:

A port guard dressing for use in connection with skin of a patient and through which a percutaneous line can pass includes an upper component, a lower component adapted to contact the skin, and at least one intermediate component positioned between the upper component and the lower component. The at least one intermediate component is attached to a lower surface of the upper component and includes or is formed from a material that is more rigid than the upper component. The material of the of the upper component intermediate component may also be more rigid than the lower component. 1. A port guard dressing for use in connection with skin of a patient and through which a percutaneous line can pass , comprising: an upper component , a lower component adapted to contact the skin , and at least one intermediate component positioned between the upper component and the lower component , the at least one intermediate component being attached to a lower surface of the upper component and comprising a material that is more rigid than the upper component.2. The port guard dressing of further comprising at least one absorbent component positioned below the at least one intermediate component and above the lower component.3. The port guard dressing of wherein the upper component comprises a passage through which the percutaneous line can pass and a slit in connection with the passage of the upper component and extending to a perimeter of the upper component claim 1 , the at least one intermediate component comprises a passage through which a percutaneous line can pass and a slit in connection with the passage of the at least one intermediate component and extending to a perimeter of the at least one intermediate component claim 1 , and the lower component comprises a passage through which a percutaneous line can pass and a slit in connection with the passage of the lower component and extending to a perimeter of the lower component claim 1 , the passage of the upper component ...

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14-01-2016 дата публикации

NEEDLE SAFETY DEVICES AND RELATED METHODS

Номер: US20160008581A1
Принадлежит: B. BRAUN MELSUNGEN AG

Safety needle assemblies, needle guards, and related methods are disclosed. The guards may be used on different needle applications to cover the tips of the needles. Exemplary needle guards are disclosed in which a curved bore profile is provided so that when the crimp or bulge on the needle retracts into the curved bore profile, the axial movement of the needle causes the needle guard to undergo a rotary movement. 1. A safety needle assembly comprising:a needle guard comprising a shroud having two arms and a drum having a bore; wherein at least one of said shroud and said bore comprises a curved profile;a needle comprising a needle shaft extending through the bore of the drum and in between the two arms; said needle shaft comprising a needle tip and a change in profile located proximally of the needle tip; andwherein the needle guard is rotatable when the change in profile is pulled through the curved profile.2. The safety needle assembly of claim 1 , wherein the shroud has a path and wherein the path is offset from the bore.3. The safety needle assembly of claim 1 , further comprising a catheter hub with a cavity and wherein the needle guard is located in the cavity of the catheter hub.4. The safety needle assembly of claim 1 , wherein the drum has a curved profile and a secure bore located proximally of the curved profile.5. The safety needle assembly of claim 1 , wherein the two arms each has a distal end and wherein the distal end has a slanted surface.6. The safety needle assembly of claim 1 , wherein the shroud is rotatable relative to the drum.7. The safety needle assembly of claim 1 , wherein the shroud has a split that separates the two arms and a continuous portion proximal of the split.8. The safety needle assembly of claim 7 , further comprising a locking slot comprising an opening formed at a proximal section of the split.9. The safety needle assembly of claim 1 , further comprising a first path through the drum and a second path through the shroud and ...

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11-01-2018 дата публикации

Reduced-Pressure, Linear-Wound Treatment Systems

Номер: US20180008470A1
Принадлежит:

A system for treating a linear wound on a patient has a closing dressing bolster for placing on the patient's epidermis over the linear wound, a sealing subsystem for providing a seal over the closing dressing bolster and the patient, and a reduced-pressure subsystem for delivering reduced pressure to the sealing subsystem. The sealing subsystem and reduced pressure subsystem are operable to deliver reduced pressure to the closing dressing bolster. The closing dressing bolster is operable under reduced pressure to develop a inward closing. The closing dressing bolster may include one or more closing members on each side of a center wound area to create the inward closing when under reduced pressure. A compressive force may also be developed. Other systems and methods are presented. 1. A closing dressing bolster for placing over a linear wound on a patient , the closing dressing bolster comprising:a top wall;a bottom wall coupled to the top wall in a spaced relationship and forming a compartment between the top wall and the bottom wall, the bottom wall having a center portion, a first lateral portion, and a second lateral portion;a plurality of beads positioned within the compartment;a first closing member formed on the first lateral portion; anda second closing member formed on the second lateral portion;wherein the first closing member has a surface formed with an oblique angle to a center plane between the first closing member and the second closing member;wherein the second closing member has a surface formed with an oblique angle to the center plane.2. The closing dressing bolster of claim 1 , wherein the top wall and the bottom wall comprise a transparent material.3. The closing dressing bolster of claim 1 , wherein the top wall and the bottom wall comprise a mesh material.4. The closing dressing bolster of claim 1 , wherein the beads comprise transparent beads.5. The closing dressing bolster of a claim 1 , wherein the beads are configured to come together over ...

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11-01-2018 дата публикации

REDUCED-PRESSURE DRESSING ASSEMBLIES FOR USE IN APPLYING A CLOSING FORCE

Номер: US20180008471A1
Принадлежит:

A closing dressing bolster and assembly for use with a system for treating a linear wound on a patient includes a bolster body formed from a flexible closing bolster material having closing members that are operable to develop an inward closing force when the closing dressing bolster is placed under reduced pressure. In one aspect, when the closing dressing bolster is under reduced pressure, the system, dressing, or assembly develops an inward force realized at the linear wound and a compression force. A wicking-material holder and wicking material may be used as well. The member components may all be see-through to allow visual inspection of the wound without requiring removal of the dressing. 1. A dressing assembly , comprising: a bolster body formed from a flexible closing bolster material,', 'a first closing member formed on a lower surface of the bolster body and including a first oblique wall,', 'a second closing member formed on the lower surface of the bolster body and including a second oblique wall; and, 'a closing dressing bolster for treating a wound, comprisingan over-drape configured to form a seal over the bolster body.2. The dressing assembly of claim 1 , wherein the bolster body is formed from silicone.3. The dressing assembly of claim 1 , wherein the bolster body is configured to develop a bending moment about a center area of the bolster body when the closing dressing bolster is placed under reduced pressure.4. The dressing assembly of claim 1 , wherein the first closing member and the second closing member are configured to move toward each other when the closing dressing bolster is placed under reduced pressure.5. The dressing assembly of claim 1 , wherein the bolster body is configured to allow light to pass through such that color may be detected from a location external to the closing dressing bolster.6. The dressing assembly of claim 1 , wherein the lower surface of the bolster body is a tissue-facing surface.7. The dressing assembly of ...

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11-01-2018 дата публикации

PACKAGING OF POWDERY MATERIAL FOR PREPARATION OF A MEDICAL SOLUTION

Номер: US20180008761A1
Принадлежит:

A package () is configured to store a powdery material () which is to be mixed with a solvent to form a medical solution, such as a dialysis solution. The package () comprises a filled cavity portion () containing the powdery material (), optionally separated into groups of different composition, and a tab portion () integrally formed with the filled cavity portion () and being swept around the filled cavity portion () so as to define a roll-up package. The tab portion () forms a protective barrier that shields the powdery material (), e.g. by counteracting transport of moisture into and out of the package. The tab portion () may also stabilize the package. The roll-up package is compact, and simple to manufacture and handle. 1. A package for storing powdery material which is to be mixed with a solvent to form a medical solution , said package comprising:a filled cavity portion containing the powdery material, anda tab portion integrally formed with the filled cavity portion and being swept around the filled cavity portion so as to define a roll-up package.2. The package of claim 1 , wherein the roll-up package is generally cylindrical.3. The package of claim 1 , wherein the tab portion is swept in at least one full turn around the filled cavity portion.4. The package of claim 1 , which defines a sealed cavity that includes the filled cavity portion and an empty cavity portion that is free of powdery material and is located adjacent to the filled cavity portion claim 1 , and wherein the tab portion includes the empty cavity portion.5. The package of claim 4 , comprising first and second overlapping sheets of flexible material which are joined to define the sealed cavity.6. The package of claim 5 , wherein the sealed cavity extends from a first cavity end to a second cavity end claim 5 , the powdery material being arranged in the sealed cavity such that the filled cavity portion is located at the first cavity end and the empty cavity portion extends from the filled ...

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10-01-2019 дата публикации

THROMBUS ASPIRATION WITH DIFFERENT INTENSITY LEVELS

Номер: US20190008626A1
Принадлежит:

Vascular treatment devices and methods include a woven structure including a plurality of bulbs that may be self-expanding, a hypotube, for example including interspersed patterns of longitudinally spaced rows of kerfs, and a bonding zone between the woven structure and the hypotube. The woven structure may include patterns of radiopaque filaments measureable under x-ray. Structures may be heat treated to include various shapes at different temperatures. The woven structure may be deployable to implant in a vessel. A catheter may include a hypotube including interspersed patterns of longitudinally spaced rows of kerfs and optionally a balloon. Laser cutting systems may include fluid flow systems. 1. A system for facilitating aspiration of a thrombus in a vessel , the system comprising:an automated motor pump configured to facilitate aspiration of the thrombus, the automated motor pump comprising an external control panel configured to receive input from an operator; andpower electronics configured to power and control the automated motor pump to generate a plurality of suction patterns having a plurality of intensity levels, a first intensity level having a first negative pressure between 100 and 350 mm Hg;', 'a second intensity level having a second negative pressure between 351 and 550 mm Hg; and', 'a third intensity level having a third negative pressure between 551 and 769 mm Hg; and, 'wherein the plurality of intensity levels compriseswherein a first crescendo suction pattern of the plurality of suction patterns comprises a repetitive cycle comprising the first intensity level for a first duration, the second intensity level for a second duration after the first duration, and the third intensity level for a third duration after the second duration.2. The system of :wherein the first duration, the second duration, and the third duration are each between 1 and 30 seconds; andwherein a total duration of the repetitive cycle of the first crescendo suction pattern ...

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10-01-2019 дата публикации

THROMBUS ASPIRATION USING AN OPERATOR-SELECTABLE SUCTION PATTERN

Номер: US20190008627A1
Принадлежит:

Vascular treatment devices and methods include a woven structure including a plurality of bulbs that may be self-expanding, a hypotube, for example including interspersed patterns of longitudinally spaced rows of kerfs, and a bonding zone between the woven structure and the hypotube. The woven structure may include patterns of radiopaque filaments measureable under x-ray. Structures may be heat treated to include various shapes at different temperatures. The woven structure may be deployable to implant in a vessel. A catheter may include a hypotube including interspersed patterns of longitudinally spaced rows of kerfs and optionally a balloon. Laser cutting systems may include fluid flow systems. 1. A system for facilitating aspiration of a thrombus in a vessel using an operator-selectable suction pattern , the system comprising:an automated motor pump configured to facilitate aspiration of the thrombus, the automated motor pump comprising an external control panel configured to receive input from an operator; andpower electronics configured to power and control the automated motor pump to generate a plurality of variable suction patterns having a plurality of intensity levels, a first intensity level having a first negative pressure; and', 'a second intensity level having a second negative pressure,', 'wherein the first negative pressure is between 551 and 769 mm Hg, and', 'wherein the first negative pressure is more negative than the second negative pressure;, 'wherein the plurality of intensity levels compriseswherein a first variable suction pattern of the plurality of variable suction patterns comprises a repetitive cycle comprising the first intensity level for a first duration and the second intensity level for a second duration after the first duration,wherein the first duration and the second duration are each between 1 and 30 seconds, andwherein a total duration of the repetitive cycle of the first variable suction pattern is between 1 minute and 15 ...

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11-01-2018 дата публикации

Method for Assembling a Drug Delivery Device and Drug Delivery Device

Номер: US20180008782A1
Принадлежит: SANOFI

A method for assembling a drug delivery device that includes mounting a cartridge with a bung, the mechanism, the plunger and the spring within a housing such that a spring biases a plunger in a dispensing direction and that a drum and/or the release member is attached to the plunger attaching a tool with torque measurement capability to the drum or a release member of a dose mechanism in a state where at least one housing part is detached from further housing part; setting a dose by rotating the dose setting member in a first direction, activating a trigger and monitoring the torque applied to the drum or the release member; releasing the trigger upon detection of a predetermined change in the torque measured by the tool; and releasing the tool and closing the housing. 1. A method of assembling a drug delivery device or components thereof comprising:providing a cartridge with a bung, a plunger, a spring biasing the plunger towards the bung and a release member coupled to the spring such that release of the spring is controlled by the release member,providing an instrument for measuring the torque or force of the spring,releasing the spring while monitoring the torque or force by the measuring instrument, andstopping the release member upon detection of a predetermined change in the torque or force measured by the measuring instrument, wherein the predetermined change in the torque or force is a rapid decrease in the torque or force due to the plunger contacting the bung in the cartridge.2. The method according to claim 1 , comprising providing a housing claim 1 , and a dose setting and dispensing mechanism comprising at least a dose setting member claim 1 , a trigger claim 1 , the release member and/or a drum claim 1 , the plunger and the spring claim 1 , which is a strained pressure spring claim 1 ,mounting the cartridge with the bung, the dose setting and dispensing mechanism, the plunger and the spring within the housing such that the spring biases the plunger ...

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14-01-2021 дата публикации

INTRAVASCULAR BLOOD PUMPS AND METHODS OF MANUFACTURE AND USE

Номер: US20210008261A1
Принадлежит:

Catheter blood pump that include an expandable pump portion extending distally from an elongate shaft. The pump portions include an expandable impeller housing including an expandable blood conduit that defines a blood lumen between an inflow and an outflow. The pump portions include one or more expandable impellers disposed at least partially within the blood lumen. 1. A catheter blood pump , comprising: an expandable impeller housing including an expandable blood conduit that defines a blood lumen between an inflow and an outflow,', 'one or more expandable impellers, each of which are disposed at least partially within the blood lumen,', 'a sensor wire secured to the expandable impeller housing and extending from a proximal end of the expandable impeller housing to a distal end of the expandable impeller housing, and', 'a sensor coupled to the sensor wire, the sensor disposed distal to a distal end of the expandable blood conduit., 'an expandable pump portion extending distally from an elongate shaft, the pump portion including'}2. The catheter blood pump of claim 1 , wherein the sensor wire is secured to the expandable impeller housing such that it is disposed radially outside of the expandable blood conduit.3. The catheter blood pump of claim 1 , wherein the sensor wire is disposed within a sensor wire lumen claim 1 , the sensor wire having a size relative to the sensor wire lumen such that it floats within the sensor wire lumen.4. The catheter blood pump of claim 3 , wherein the sensor wire lumen is defined by an inner surface of an elongate hollow shaft claim 3 , the elongate hollow shaft secured to the expandable impeller housing.5. The catheter blood pump of claim 4 , wherein the elongate hollow shaft has a circular cross sectional configuration.6. The catheter blood pump of claim 4 , further comprising an overlay disposed about the elongate hollow shaft claim 4 , the overlay positioned to secure the elongate hollow shaft relative to the expandable impeller ...

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11-01-2018 дата публикации

MEDICAL CONNECTOR

Номер: US20180008813A1
Принадлежит: TERUMO KABUSHIKI KAISHA

A medical connector of the present invention is characterized in that: when a male connector portion is inserted into a female connector portion, a first locking portion is engaged with the female connector portion to achieve a first locked state as well as a second locked state; when the second locked state is released by operation of a second unlock operating portion and the female connector portion is moved in a disengagement direction with respect to the male connector portion, the locking member is moved in the disengagement direction together with the female connector portion while keeping the first locked state; and when the female connector portion is rotated with respect to the male connector portion, the first locked state is released. 1. A medical connector comprising:a connector body comprising a male connector portion and a cover portion surrounding an outer periphery of the male connector portion;a locking member located inside the cover portion and being movable with respect to the cover portion within a predetermined range in a direction along an axis of the male connector portion, the locking member comprising a first locking portion;a second locking portion; anda second unlock operating portion;wherein the first locking portion is configured to engage with a female connector portion of another medical connector and to bring the female connector portion into a first locked state,wherein the second locking portion is configured to, while the female connector is in the first locked state, bring the female connector portion into a second locked state in which the female connector portion cannot be moved in a disengagement direction with respect to the male connector portion,wherein the second unlock operating portion is configured to release the female connector from the second locked state,wherein, when the male connector portion is inserted into the female connector portion, the female connector portion is brought into the first locked state and the ...

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14-01-2021 дата публикации

Patch-Sized Fluid Delivery Systems and Methods

Номер: US20210008279A1
Автор: Gray Larry B.
Принадлежит:

A patch-sized fluid delivery device may include a reusable portion and a disposable portion. The disposable portion may include components that come into contact with the fluid, while the reusable portion may include only components that do not come into contact with the fluid. Redundant systems, such as redundant controllers, power sources, motor actuators, and alarms, may be provided. Alternatively or additionally, certain components can be multi-functional, such a microphones and loudspeakers that may be used for both acoustic volume sensing and for other functions and a coil that may be used as both an inductive coupler for a battery recharger and an antenna for a wireless transceiver. Various types of network interfaces may be provided in order to allow for remote control and monitoring of the device. 1. A method for delivering an infusion medium to a user , the method comprising:providing a first housing portion and a second housing portion;providing the first housing portion and the second housing portion with connection structure to allow the first housing portion and the second housing portion to be selectively engaged with each other for operation and disengaged from each other to allow disposal of the first housing portion without disposing of the second housing portion;providing a pumping assembly;providing a first exit valve in the pumping assembly wherein the first exit valve inhibits fluid flow from a reservoir to a pump exit;providing a dispensing assembly downstream from the pumping assembly, and in fluid communication with the reservoir by a flow line;providing an exit assembly downstream from the dispensing assembly, the exit assembly in fluid communication with the pump exit: andmaintaining the infusion medium in the first housing portion so as to not contact the second housing portion.3. A method according to claim 1 , wherein the one-way valve comprises a duckbill valve structure.4. A method according to claim 1 , further comprising connecting ...

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14-01-2021 дата публикации

SYRINGE, SYRINGE ASSEMBLY, AND MANUFACTURING METHOD OF SYRINGE

Номер: US20210008285A1
Автор: Okihara Hitoshi
Принадлежит: TERUMO KABUSHIKI KAISHA

A syringe of a syringe assembly is provided with a body portion capable of being filled with a drug solution and a female port nozzle portion which extends from a distal end of the body portion and includes a communication port on a proximal end of the female port nozzle. The body portion includes a distal end wall surface and a side wall surface to which a liquid lubricant is applied. The distal end wall surface includes a concave portion arranged radially outside an inner edge portion adjacent to the communication port and concave in a distal end direction more than at least a part of the inner edge portion, and the concave portion is arranged to fully surround the communication port and may store the liquid lubricant. 1. A syringe comprising:a body portion including an inner cavity configured to be filled with a drug solution;a female port nozzle portion that extends from a distal end of the body portion into which a male luer is inserted;a proximal end opening formed on a proximal end portion of the body portion;the female port nozzle portion including a communication port through which an inner portion of the female port nozzle portion is communicated with the inner cavity of the body portion on a proximal end of the female port nozzle portion; and a distal end wall surface that extends radially outward from the communication port of the female port nozzle portion and faces the inner cavity; and', 'a side wall surface that extends from an outer edge of the distal end wall surface in a proximal end direction and faces the inner cavity;, 'the body portion includes an inner edge portion adjacent to the communication port of the female port nozzle portion; and', 'a concave portion arranged radially outside the inner edge portion and is concave in a distal end direction more than at least a part of the inner edge portion; and, 'the distal end wall surface of the body portion includesa liquid lubricant is applied on the side wall surface of the body portion, and ...

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27-01-2022 дата публикации

Hygienic Medical Devices Having Hydrophilic Coatings and Methods of Forming the Same

Номер: US20220023508A1
Принадлежит:

Hygienic Hydrophilic coatings, hydrophilic coating formulations and wetting fluids that include an anti-infective agent. 1. A lubricous hydrophilic catheter assembly , comprising:a gas impermeable and liquid impermeable package having a sealed cavity;a catheter having a hydrophilic coating located within the sealed cavity; anda wetting fluid comprising a wetting agent and mannose located within the sealed cavity.2. The catheter assembly of claim 1 , wherein the wetting fluid further includes a peroxide generating enzyme.3. The catheter assembly of claim 2 , wherein the enzyme comprises an oxidoreductase.4. The catheter assembly of claim 2 , wherein the enzyme comprises glucose oxidase.5. The catheter assembly of claim 2 , wherein the enzyme comprises peroxidase.6. The catheter assembly of wherein the peroxidase comprises lactoperoxidase.7. The catheter assembly of claim 1 , wherein the hydrophilic coating comprises a hydrophilic polymer matrix.8. The catheter assembly of claim 7 , wherein a hydrophilic polymer of the hydrophilic polymer matrix comprises polyvinylpyrrolidone.9. The catheter assembly of claim 1 , wherein the hydrophilic coating further comprises an antioxidant.10. The catheter assembly of wherein the hydrophilic coating further comprises a thixotropic agent.11. The catheter assembly of wherein the thixotropic agent comprises pectin claim 10 , agar and/or alginate.12. The catheter assembly of wherein the wetting fluid further comprises sugar alcohol.13. The catheter assembly of claim 12 , wherein the sugar alcohol is xylitol.14. The catheter assembly of wherein the hydrophilic coating or wetting fluid further comprises an organic acid.15. A method of forming a lubricous hydrophilic catheter assembly claim 1 , comprising:inserting a catheter having a hydrophilic coating into a gas impermeable and liquid impermeable package having a cavity;placing a wetting fluid comprising a wetting agent and mannose into the cavity; andsealing the cavity.16. The method ...

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14-01-2021 дата публикации

Multi-Stage Nasal Filter and Method Of Tuning The Filter To A Predetermined Most Penetrating Particle Size

Номер: US20210008397A1
Принадлежит: Individual

Respiratory devices and methods for their manufacture and use are disclosed. The device features a resiliently deformable element configured to form a perimeter seal with the inner nostril wall and to swab the distal portion of the internal nostril region with a disinfectant during device installation. A first filter stage includes a first filter layer characterized by first geometric convolutions and a first MPPS1 value; and a second filter stage includes a second filter layer characterized by second geometric convolutions and a second MPPS2 value.

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27-01-2022 дата публикации

On-line drying of hollow fiber membranes

Номер: US20220023803A1
Принадлежит: GAMBRO LUNDIA AB

The present invention relates to a continuous process for preparing permselective hollow fiber membranes being suitable e.g. for hemodialysis, hemodiafiltration and hemofiltration of blood which comprises a two-stage drying and tempering treatment of the hollow fiber membranes. According to a further aspect, the invention relates to a continuous process for drying permselective hollow fiber membranes on-line. The invention also relates to devices for on-line drying of permselective hollow fiber membranes.

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09-01-2020 дата публикации

Face soaking device

Номер: US20200009360A1
Автор: John Richard Taylor
Принадлежит: Individual

Face soaking devices (devices) may include a vessel and a vessel neck gasket. The vessel may be configured to hold a liquid to submerge a face of a user or a portion thereof. The vessel neck gasket may be (removably) joined to the vessel. The vessel neck gasket may be configured to comfortably accommodate a portion of the user's neck. The devices may include a breathing apparatus that may be in removable contact with: the vessel, with a head rest subassembly, and/or with the user. The breathing apparatus may be configured to permit the user to breathe while the user's face may be submerged within the liquid. When the vessel may be filled with the liquid to at least a sufficient level, the user may soak the face or the portion thereof, such that the skin being soaked receives a benefit.

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09-01-2020 дата публикации

MICRO NEEDLE

Номер: US20200009361A1
Принадлежит: GL.company

A micro needle includes: a first base; a second base formed integrally with the top surface of the first base; a needle support formed integrally with the top surface of the second base and leading to a tapered groove penetrating the bottom surface of the first base; and a needle body formed integrally with the center of the top surface of the needle support and having a needle hole leading to the tapered groove. The micro needle allows for low-cost mass production because of the simple structure, and involves applying various drugs by injecting drugs after puncturing the skin. 1. A micro needle comprising:a first base;a second base formed integrally with the top surface of the first base;a needle support formed integrally with the top surface of the second base and leading to a tapered groove penetrating the bottom surface of the first base; anda needle body formed integrally with the center of the top surface of the needle support and having a needle hole leading to the tapered groove.2. The micro needle of claim 1 , wherein the first and second bases are disc-shaped claim 1 , and the needle support is cone-shaped.3. The micro needle of claim 1 , wherein the needle support is 1.3 to 1.7 mm long claim 1 , the maximum inner diameter of the tapered groove is 1.5 to 2.5 times the outer diameter of the needle support claim 1 , and the top inner diameter of the tapered groove is 1.5 to 3 times the outer diameter of the needle body.4. The micro needle of claim 1 , wherein the needle body is 0.1 to 1.0 mm long claim 1 , with an outer diameter of 40 to 300 μm claim 1 , and the needle hole has an inner diameter of 30 to 250 μm.5. The micro needle of claim 1 , wherein the needle hole is punched from the bottom of the needle support using a micro drill. This U.S. non-provisional patent application claims priority under 35 U.S.C. § 119 of Korean Patent Application No. 10-2018-0077388, filed on Jul. 4, 2018, the entire contents of which are hereby incorporated by reference.The ...

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09-01-2020 дата публикации

Microneedle template and microneedle prepared using the same

Номер: US20200009363A1
Принадлежит: S-Skin Co Ltd

Provided are a microneedle template including: a substrate on which at least one microneedle shapes are formed; and a diamond layer formed on the surface of the at least one microneedle shapes, a method for preparing the microneedle template, a microneedle prepared using the microneedle template, and a method for preparing the microneedle.

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09-01-2020 дата публикации

Method and Device for Manufacturing Dissolving Microneedle

Номер: US20200009767A1
Автор: LI Chengguo
Принадлежит:

A method and a device for manufacturing dissolving microneedle, wherein the method comprises manufacturing a mold with a plurality of microporous cavities, and manufacturing a polymer solution to be sprayed into the microporous cavity by a high pressure spraying device to enable the sprayed solution to fill in each microporous cavity. After the dryness of the solution, a microneedle is extracted from the mold. The process for manufacturing the microneedle is without vacuum pumping or any load of centrifugal force, and the process is simple and the excellent rate is high. 1. A method for manufacturing dissolving microneedle , comprising manufacturing a microneedle mold , said microneedle mold has a plurality of microporous cavities , wherein a polymer solution is sprayed into the microporous cavity by a high pressure spraying device to enable the polymer solution to fill into each of the microporous cavities; and the solidified microneedle are extracted from the microneedle mold after the dryness of polymer solution.2. The method for manufacturing dissolving microneedle according to claim 1 , wherein said polymer solution sprayed into the microporous cavity by the high pressure spray device comprises the atomized polymer solution sprayed into the microporous cavity by a high pressure atomizing device.3. The method for manufacturing dissolving microneedle according to claim 2 , wherein the particle size of said atomized polymer solution sprayed by the high pressure atomizing device ranges from 0.1 to 100 micrometers.4. The method for manufacturing dissolving microneedle according to claim 1 , wherein said polymer solution sprayed into the microporous cavity by the high pressure spray device comprises the droplets of the polymer solution sprayed to the microporous cavity by the high pressure spotting device.5. The method for manufacturing dissolving microneedle according to claim 4 , wherein the particle size of said droplets of the polymer solution sprayed by the high ...

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08-01-2015 дата публикации

Expandable Inter Vivos Tube and Method of Manufacturing Same

Номер: US20150011828A1
Принадлежит:

A flexible expandable inter vivos tube includes at least one arched segmented portion, a corresponding movable element and at least one positioning mechanism. The at least one arched segmented portion and corresponding movable element forming a flexible closed longitudinally expandable tube. The at least one arched segment includes an H-shaped connector having at least one cavity that allows variable slidable movement of a free end portion of the corresponding movable element. A balloon is contained in each of the at least one cavity so that the hydraulic or air pressure within balloon expands the movable element and, thus, the circumference of the flexible inter vivos tube is increased. 2. The inter vivos tube of claim 1 , further comprising:sealing means associated with each of a distal end of said flexible member and a proximal end of said flexible member.3. The inter vivos tube of claim 1 , wherein said first free end and said second free end are tapered.4. The inter vivos tube of claim 1 , wherein said balloon comprising a material having an expansion capability greater at a distal end of said balloon than at a proximal end of said balloon.5. The inter vivos tube of claim 1 , wherein said rib has a greater width at a distal end of said flexible member than at a proximal end of said flexible member.6. The inter vivos tube of claim 1 , wherein said injection ports are at substantially one of: a distal end and a proximal end of said flexible member.7. The inter vivos tube of claim 6 , wherein said insertion ports are in one of: said outer circumference member and said inner circumference member.8. The inter vivos tube of claim 1 , further comprising;a plurality of serrations on each of said first free end and said second free end; anda retaining pin positioned on at least a portion of an edge of one of: the lower circumference member and the outer circumference member, said retaining pin positioned opposite said plurality of serrations.9. The inter vivos tube of ...

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15-01-2015 дата публикации

ORAL AIRWAY ADJUNCT AND METHOD FOR MAKING THE SAME

Номер: US20150013672A1
Автор: Abdoue Akram
Принадлежит:

An oral airway adjunct includes a passageway extending from the proximal end to the distal end, wherein the passageway is sized to pass through a breathing tube. The oral airway adjunct also includes a flange located at the proximal region and a curved region extending away from the proximal region towards the distal region. The curved region is defined by a varying radius. 1. An oral airway adjunct including a proximal end , a distal end , a proximal region , a distal region , a superior side , and an inferior side , wherein the oral airway adjunct comprises:a passageway extending from the proximal end to the distal end, wherein the passageway is sized to pass through a breathing tube;a flange located at the proximal region; anda curved region extending away from the proximal region towards the distal region,wherein the curved region is defined by a varying radius.2. The oral airway adjunct of claim 1 , wherein an axial cross-section of the passageway is constant along the length of the passageway.3. The oral airway adjunct of claim 1 , wherein an axial cross-section of the passageway narrows in the distal region claim 1 , thereby defining a ramp in the passageway.4. The oral airway adjunct of claim 3 , wherein the ramp extends away from the superior side towards the inferior side.5. The oral airway adjunct of claim 3 , wherein the distal end comprises a bevel.6. The oral airway adjunct of claim 5 , wherein:a long end of the bevel is located on the inferior side; anda short end of the bevel is located on the superior side.7. The oral airway adjunct of claim 1 , wherein the distal end comprises a bevel.8. The oral airway adjunct of claim 7 , wherein:a long end of the bevel is located on the inferior side; anda short end of the bevel is located on the superior side.9. The oral airway adjunct of claim 1 , wherein the oral airway adjunct is formed with a material comprising polyvinyl chloride (PVC).10. A method for creating an oral airway adjunct for use in an airway ...

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15-01-2015 дата публикации

PATIENT INTERFACE DEVICE HAVING AN ENGINEERED SURFACE FOR PROVIDING LOW FRICTION AND IMPROVED COMFORT TO THE USER

Номер: US20150013682A1
Принадлежит:

A patient interface device includes an elastomeric contacting portion that is structured to directly engage the skin of the user. The contacting portion has an engineered surface that includes a plurality of non-random, predesigned surface features designed to reduce friction and improve user comfort. In one implementation, the pitch between each immediately adjacent pair of the surface features is less than or equal to a predetermined maximum pitch value, and the height of each of the surface features is less than or equal to a predetermined maximum height value. 1. A patient interface device , comprising:a contacting portion structured to directly engage a user's skin during use of the patient interface device, wherein at least a section of the contacting portion has an engineered surface comprising a plurality of non-random, predesigned surface features each having a like geometry, wherein in the section a pitch between each immediately adjacent pair of the surface features is (i) equal, or demonstrates anisotropic pitch such that the pitch between each immediately adjacent pair of the surface features in a first direction is equal to a first pitch value and the pitch between each immediately adjacent pair of the surface features in a second direction transverse to the first direction is equal to a second pitch value different than the first pitch value, and (ii) less than or equal to a predetermined maximum pitch value, wherein the predetermined maximum pitch value is any of: (i) 50 microns, (ii) 100 microns, or (iii) greater than or equal to 10 microns and less than or equal to 100 microns, or wherein the pitch between each immediately adjacent pair of the surface features in any of: (i) greater than or equal to 10 microns and less than or equal to 50 microns, or (ii) greater than or equal to 20 microns and less than or equal to 50 microns, and wherein in the section a height of each of the surface features is less than or equal to a predetermined maximum ...

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15-01-2015 дата публикации

HOLLOW STRUCTURE FOR BREATHING MASK

Номер: US20150013683A1
Принадлежит:

A hollow structure for a face mask includes an inner wall, an outer wall spaced from the inner wall to define a hollow area between the inner wall and the outer wall, and a bottom wall that couples the inner wall to the outer wall. A first portion and a second portion together define a closable opening into the hollow area. The second portion is coupled to the outer wall by a bi-stable membrane that allows the second portion to move between (1) a first, opened position in which the second portion is spaced from the first portion to allow access to the hollow area through the opening, and (2) a second, closed position in which the second position abuts the first portion to close the opening. 127-. (canceled)28. A hollow structure , comprising:an inner wall;an outer wall spaced from the inner wall to define a hollow area between the inner wall and the outer wall;a bottom wall that couples the inner wall to the outer wall; anda first portion and a second portion which together define a closable opening into the hollow area, the second portion being coupled to the outer wall by a membrane that allows the second portion to move between (1) a first, opened position in which the second portion is spaced from the first portion to allow access to the hollow area through the opening, and (2) a second, closed position in which the second position abuts the first portion to close the opening.29. The hollow structure of claim 28 , wherein the membrane is a bi-stable membrane that is movable between a first position in which the opening is open and a second position in which the opening is closed.30. The hollow structure of claim 28 , wherein the hollow structure is a cushion for a breathing mask.31. The hollow structure of claim 30 , further comprising an end portion arranged to form a contact zone configured to rest against a patient's face.32. The hollow structure of claim 31 , wherein the end portion is configured to seal against the patient's face.33. The hollow structure of ...

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15-01-2015 дата публикации

Reservoir or medicated module for a drug delivery system and method of and assembly for filling the same

Номер: US20150013827A1
Автор: Bernd Kuhn
Принадлежит: SANOFI SA

A reservoir for a drug delivery system is provided, wherein the reservoir comprises a cavity, the cavity being filled with a dose of a fluid drug such that the dose of the drug occupies 95% or more of the cavity, wherein the dose volume is less than 5 ml. Furthermore, a method for filling a reservoir for a drug delivery system is provided.

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03-02-2022 дата публикации

Dispensing outlet, dispensing system, method of using a dispensing system, injection mold and method of producing a dispensing outlet

Номер: US20220031963A1
Принадлежит: Sulzer Mixpac AG

A dispensing outlet includes a housing with a first end of the housing having a first outlet and a second end of the housing having a mixing or reception space. The mixing or reception space is configured to receive a further component, and a pre-determined breaking point is formed between the first outlet and the mixing or reception space.

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03-02-2022 дата публикации

CAPSULE RETAINING SYSTEM

Номер: US20220031970A1
Принадлежит:

A holding device including a sleeve wall having an outer wall surface and an inner wall surface. The inner wall surface forms a capsule insertion channel extending through an entirety of the sleeve wall. A lip is at an end of the capsule insertion channel and extends toward a center of the capsule insertion channel. The inner wall surface has a recess at a first distance along the inner wall surface from the lip, a base extending outward from the outer wall surface of the sleeve wall; and a flexible retaining element in the recess. The recess being configured to prevent movement of the flexible retaining element along the inner wall. The flexible retaining element having a cross-sectional profile with a first width at a side closer to the lip, and a second width at a side farther from the lip, the first width being larger than the second width. 1. A holding device , comprising: an outer wall surface and', 'an inner wall surface, wherein the inner wall surface forms a capsule insertion channel extending through an entirety of the sleeve wall, and wherein a lip is at an end of the capsule insertion channel, the lip extending toward a center of the capsule insertion channel, the inner wall surface having a recess at a first distance along the inner wall surface from the lip;, 'a sleeve wall having'}a base extending outward from the outer wall surface of the sleeve wall at a same end of the sleeve wall as the lip;an annular seal against the lip and within the capsule insertion channel; and 'the flexible retaining element has a cross-sectional profile with a first width at a side closer to the lip, and a second width at a side farther from the lip, wherein the first width is larger than the second width.', 'the recess is configured to prevent movement of the flexible retaining element along the inner wall with respect to the lip, and wherein'}, 'a flexible retaining element in the recess, wherein,'}2. The holding device of claim 1 , wherein the inner wall surface further ...

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03-02-2022 дата публикации

PATIENT INTERFACE SYSTEM AND COMPONENTS THEREFOR

Номер: US20220031990A1
Автор: Goh Sok Li
Принадлежит:

A patient interface system which includes a magnetic fastener arrangement to connect a positioning and stabilising structure to a patient interface, a positioning and stabilising structure having at least one strap and a magnetic fattener component provided to the strap. The magnetic fastener component is provided between a distal end of the strap and an anterior portion of the positioning and stabilising structure, and can be formed to the strap. 1. A positioning and stabilising structure for a patient interface system , comprisinga rear strap assembly,at least one strap which extends away from the rear strap assembly and along a side of the patient's face, wherein the at least one strap has a distal end, anda first strap fastener that comprises a magnetic fastener component provided to the at least one strap and that is positioned between the distal end and the rear strap assembly.2. A positioning and stabilising structure for a patient interface system , comprising at least one strap and a strap fastener half , wherein the strap fastener half comprises a magnetic fastener component which is formed to the at least one strap.3. A positioning and stabilising structure for a patient interface system , comprising at least one strap and a strap fastener half which is permanently attached to the positioning and stabilising structure , wherein the strap fastener half comprises a magnetic fastener component , and further wherein the strap fastener half is configured to in use engage with a corresponding fastener half on a patient interface to attach the positioning and stabilising structure to the patient interface.4. The positioning and stabilising structure as claimed in claim 1 , comprising a first strap and a second strap claim 1 , wherein the first strap comprises a first strap fastener half and the second strap comprises a second strap fastener half claim 1 , and further wherein the first strap fastener half and the second strap fastener half each comprises a ...

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03-02-2022 дата публикации

Immersive distraction therapy

Номер: US20220031997A1
Принадлежит: BioVentures LLC

Disclosed herein is an immersive distraction apparatus including an attachment portion including an engagement element and a front plate having two cut outs fitting lenses therein and a base portion coupled with the attachment portion having a display aperture sized to receive a device. The immersive distraction apparatus mountable on a surgical head frame using one or more connectors such that an immersive distraction therapy can be provided to a patient undergoing surgery via a virtual reality environment.

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03-02-2022 дата публикации

Microminiature EM Coil Sensor Pull Ring For Catheter

Номер: US20220032011A1
Принадлежит:

A microminiature electro-magnetic coil sensor pull ring with a pull wire attached thereto is used in changing the angle of a distal end of a medical catheter. The tubular pull ring has a connection recess with a flat bottom machined into the full wall thickness and located proximal to a coil wrap area. Circuit wires are electrically connected to the two lead ends of the coil within the connection recess, such that neither the circuit wires nor the lead ends stand proud of the full wall thickness. The coil wrap area is also recessed, and can have side walls defining an offset angle for the turns of the coil. In another aspect, a coil is wound around one of the pull wires for the pull ring. 1. A microminiature electro-magnetic coil sensor pull ring for use in a medical catheter , comprising:a tubular pull ring having a full wall thickness, the pull ring having a coil wrap area about a longitudinal axis, the pull ring having a connection recess into the full wall thickness and located proximal to the coil wrap area, the pull ring having at least one pull wire connection location into the full wall thickness and located proximal to the coil wrap area;a coil formed of a flexible, electrically insulated metal wire wrapped about the coil wrap area with a plurality of turns for sensing through human tissue, the wire being smaller than 40 AWG, the wire terminating in two lead ends extending flexibly from the turns;at least one pull wire connected to the pull ring within the pull wire connection location, for changing the angle of the pull ring for navigation of the medical catheter through human tissue;circuit wires electrically connected to the two lead ends within the connection recess, such that neither the circuit wires nor the lead ends stand proud of the full wall thickness.2. The microminiature electro-magnetic coil sensor pull ring of claim 1 , wherein the connection recess has a flat bottom surface.3. The microminiature electro-magnetic coil sensor pull ring of ...

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03-02-2022 дата публикации

Nasal drug delivery system

Номер: US20220032022A1
Принадлежит: Leland Stanford Junior University

Devices, systems, and methods for treating chronic rhinosinutisits (CRS) are described herein. The devices can have a guide member defining at least one lumen therethrough. A drug delivery component is advanced through the lumen to deliver a substance to the sino-nasal cavity of a patient. Once the drug delivery component is positioned at the desired area in the sino-nasal cavity, a user actuates the system to deliver the substance to the target area. Actuation of the system delivers the substance to the middle meatus, osteo-meatal complex, or other areas within the sino-nasal cavity of the patient.

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09-01-2020 дата публикации

Device and Method for Detecting an Actuation Action Performable with a Medical Device

Номер: US20200013503A1
Принадлежит:

An apparatus is disclosed, comprising a detector unit comprising a detector configured to detect an actuation action performable via the detector unit to an actuation button of a medical device to cause the medical device to eject at least a portion of a medicament comprised in the medical device. The detector is configured to detect the actuation action based on a detection of a force and/or a touch applied to the detector unit as part of the actuation action. The apparatus further comprises an electric unit connected to the detector and configured to store and/or provide information related to the detected actuation action. Furthermore, an according method and a computer program for controlling this method are disclosed. 12. An apparatus () , comprising:{'b': 20', '21', '22', '23', '21', '20', '21', '22', '23', '11', '1', '1', '1', '21', '20', '21', '22', '23, 'a detector unit (, , , ) comprising a detector () configured to detect an actuation action performable via said detector unit (, , , ) to an actuation button () of a medical device () to cause said medical device () to eject at least a portion of a medicament comprised in said medical device (), wherein said detector () is configured to detect said actuation action based on a detection of a force and/or a touch applied to said detector unit (, , , ) as part of said actuation action, and'}{'b': '22', 'an electric unit () connected to said detector and configured to store and/or provide information related to said detected actuation action.'}222120212223212120212223. The apparatus () according to claim 1 , wherein said force acts on said detector () directly or via a part of said detector unit ( claim 1 , claim 1 , claim 1 , ) claim 1 , or is detected by said detector () because said detector () is responsive to a movement and/or a deformation of at least a part of said detector unit ( claim 1 , claim 1 , claim 1 , ) caused by said force.3221. The apparatus () according to any of the preceding claims claim 1 ...

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