Abstract: A tip cap including a central body extending between a first end and a second end. The first end includes a syringe coupling and the second end can include a projection or pivot. In example embodiments, axial engagement of an end connector of a syringe with the syringe coupling self-connects the tip cap with the end connector of the syringe while rotating about the pivot. According to example embodiments, a flange extends outwardly from the central body to define a width or side-to-side dimension. In example embodiments, the minimum side-to-side dimension is about 1.25 inches.

Abstract: Disclosed herein are systems and methods for monitoring performance of an ambulatory infusion pump. An ambulatory infusion pump can include a reservoir configured to contain a medicament including a plunger at a proximal end of the reservoir and an outlet port at a distal end of the reservoir. A motor can be configured to cause linear motion of a pushrod to contact and move the plunger to cause medicament to flow from the reservoir out of the outlet port to a patient. An optical encoder can be employed to monitor a linear position of the pushrod. In addition, the optical encoder can be employed to monitor additional system conditions and/or a secondary encoder can be employed to monitor the performance of the optical encoder.

Abstract: In the specification and drawings a method and apparatus for delivering a drug into a nasal turbinate or nasal polyp is described and shown, which can include implanting a drug eluting implant into a nasal turbinate or nasal polyp; and leaving the drug eluting material in the nasal turbinate or nasal polyp for at least one day such that a drug is released from the drug eluting implant over a period of time.

Abstract: In some examples, an aspiration catheter system includes an outer catheter and an inner catheter configured to be positioned within the outer catheter lumen, and an alignment element. The outer catheter defines an outer catheter lumen and an outer catheter distal opening. The inner catheter defines an inner catheter lumen, an inner catheter distal opening, and a plurality of sidewall openings proximal to the inner catheter distal opening. The alignment element is configured to indicate a predetermined position of the inner catheter relative to the outer catheter when the inner catheter is received within the outer catheter distal opening. When the inner catheter is at the predetermined position, at least one sidewall opening of the plurality of sidewall openings remains positioned within the outer catheter lumen and at least one other sidewall opening of the plurality of sidewall openings is positioned distal to the outer catheter distal opening.

Abstract: A gasket suitable for a syringe stopping with vacuum is provided. The gasket is compatible with sliding property within the sleeve and water-tightness of the syringe barrel after exiting the sleeve. The gasket includes a gasket body made of a liquid-resistant hard plastic having a tip surface contacting medicinal solution and a concave groove formed on a side surface facing an inner peripheral surface of a syringe barrel and formed continuously to the tip surface contacting medicinal solution; and a sliding contact ring made of an elastic material fitted in the concave groove. Then, an outer diameter D1 of a peripheral end of a tip portion including the tip surface contacting medicinal solution of the gasket body is set to be larger than the outer diameter D4 of the sliding contact ring.

Abstract: An oral dispensing device includes a main body for holding liquid and a guard, the main body being straight, elongated and having a longitudinal axis, and capable of dispensing the held liquid from one end. The guard is set upon the main body with a front portion of the main body protruding from the front of the guard. The guard is shaped such that when the front portion is placed in a mouth of a subject, the guard lies against the front of a face of the subject, such that if the front of the face of the subject is considered as a plane, the longitudinal axis of the liquid holding body is inclined to the plane of the face.

Abstract: A medicament container for a syringe or carpule has a base body surrounding an interior at least in sections. The base body has a central axis and a proximal opening. An end plug is arranged in the interior such that the end plug in the interior is displaceable along the central axis and separates a first proximal region of the interior from a second distal region of the interior. A plug securing part is at least partially insertable into the second region through the proximal opening. When inserted into the interior, the plug securing part is arranged closer to the proximal opening than the end plug and is fixedly held in the interior by the positive and/or non-positive connection at least in a holding area.

Abstract: Implementations of the present disclosure are directed to an injection device (102) that includes a medicament reservoir (103), a stopper (105) including a rigid core (125) and an ultrasound probe (122) disposed in a housing, the ultrasound probe configured to transmit an emitted ultrasound signal through the rigid core along a longitudinal direction of the rigid core into the medicament reservoir and to receive an ultrasound signal generated by reflections of the emitted ultrasound signal, the reflections including at least a reflection from a distal end of the medicament reservoir, a control component (124a) configured to be electronically coupled with the ultrasound probe and to process the ultrasound signal to generate injection device data, and an antenna (124c) configured to be electronically coupled with the control component and to transmit the injection device data to an external computing device (104).

Abstract: A medical device is disclosed including a needle guide. The needle guide includes abase, a guide member, and a handle arrangement. The base defines a base channel and the guide member includes a guide member channel in communication with one another and configured for receiving a flexible needle. The guide member includes a non-linear portion and is generally flexible to accommodate passage of a flexible needle through a corresponding portion of the guide member channel. The handle arrangement is configured to accommodate stabilization of the needle guide during deployment.

Abstract: A medicament delivery device comprising: a housing arranged to contain a medicament container with a piston for sealing the medicament container and displacing the medicament; a medicament delivery mechanism arranged to push the piston to displace the medicament when activated; and a driving mechanism connected to the medicament delivery mechanism such that when the medicament delivery mechanism is activated, the driving mechanism converts linear motion of the medicament delivery mechanism into torque so as to rotate a rotation member.

Abstract: The invention relates to a transdermal therapeutic system (TTS) for delivering pharmaceutical active ingredients. The TTS includes a cover layer and at least one active-ingredient-containing carrier material. At least one retaining element is located between the active-ingredient-containing carrier material and the cover layer, with the retaining element fixing the active-ingredient-containing carrier material onto the cover layer. The invention further relates to a method for fastening an active-ingredient-containing carrier material to a cover layer of a TTS in the presence of hook-and-loop strip segments and the use of a hook-and-loop strip in transdermal or iontophoretic administration of pharmaceutical or therapeutic active ingredients to patients.

Abstract: A system to be implanted in a living body for supplying medical substance, such as insulin. The system has a first module (1) having an inlet port (5) for receiving a transcutaneous injection of the medical substance, a second module (2) having a reservoir for storing the medical substance; a first tube (3) allowing the medical substance to flow between the first module and the second module; and a catheter (4) for releasing the stored medical substance into the living body. The first tube (3) allows the first module and second module to be implanted at different locations in the living body.

Abstract: The present disclosure relates generally to the field of minimally invasive catheter-based devices and procedures for the removal of necrotic debris. In particular, the present disclosure relates to systems and methods for the removal of necrotic debris from within a walled off necrosis without disrupting or damaging the tissue wall of the necrotic pocket.

Abstract: An injection device including a barrel having a medicament reservoir therein capable of fluid communication with a needle assembly at a distal end thereof and sealed at a proximal end thereof with a stopper. The injection device further includes a plunger rod having a distal rod end which is couplable with said stopper, wherein, when the plunger rod is coupled to the stopper, forward axial movement of the plunger rod causes forward axial movement of the stopper coupled thereto into the medicament reservoir in order to expel medicament through the needle assembly. Further, the plunger rod can be decoupled from the stopper by applying a rearward axial force on the plunger rod, said rearward axial decoupling force being less than a rearward axial force required to move the stopper rearwardly with respect to the barrel.

Abstract: A method comprises positioning a medical appliance having a primary pressure sensor at or within a patient incision site and supplying an insufflation fluid to the patient cavity. The method further comprises measuring a pressure in the patient cavity by the primary pressure sensor and controlling the supply of insufflation fluid by an insufflator to the patient cavity based at least on the measured pressure. The method further comprises determining, by a processor associated with the insufflator, that the measured pressure may be inaccurate and, in response to determining that the measured pressure may be inaccurate, controlling, by the insufflator, the supply of the insufflation fluid to the patient cavity based at least on a pressure measured by a backup pressure sensor.

Abstract: The present invention relates to an assembly comprising an injection device comprising a container for a product, wherein the container includes a distal tip encompassing a channel providing a passageway for transferring the product, and an adaptor mounted onto the distal tip. The assembly further includes a heat-shrinkable film covering at least part of the container and at least part of the adaptor, wherein the heat-shrinkable film maintains the adaptor blocked in rotation and in translation relative to the container when the heat-shrinkable film is in heat-shrunk condition.

Abstract: An autoinjector apparatus is disclosed which comprises a single-use cassette and an autoinjector. The cassette comprises a housing and a sleeve movably disposed in the housing. A syringe may be disposed in the sleeve and secured therein with a lock cap. The lock cap is affixed to a distal end of the sleeve and contacts the distal end of the syringe. A shield remover extends through an opening in a proximal end of the housing for removing a needle shield which covers a needle of the syringe. A cassette identification arrangement is provided on a surface of the housing to enable the autoinjector to identify the cassette. The autoinjector is provided with a detector for reading the cassette identification arrangement.

Abstract: The invention relates to a safety assembly for preventing needle stick injury with a needle having a proximal end fixed to a tip of a medical container and a pointed distal end, the safety assembly having: an attachment ring fixed to the tip of the container and a safety device to cover at least the distal end of the needle, the safety device attached to the attachment ring. The safety assembly has an attachment ring having an inner ring and an outer ring to be snapped onto each other, the inner ring having an inner recess for applying glue between the inner ring and the tip, and the inner ring and outer ring having mutually engaging elements preventing any rotation of the outer ring relative to the inner ring.

Abstract: A vaporizing device for consuming a stimulant or a pharmaceutical substance by inhaling a vapour comprise a housing having an exit opening provided at one end of said housing, a vaporizer connected to said exit opening via a vapour conduit, said vaporizer having an electrically driven heating unit and a liquid exposure section that is heated by the heating unit to vaporize a liquid in said liquid exposure section, a liquid reservoir connected to said liquid exposure section via a liquid conduit, and an electrical energy storage unit electrically connected to said heating unit, wherein an electrical fluid level sensor is associated with said liquid reservoir, said fluid level sensor being arranged and adapted to produce a low-level-signal if the liquid level within said liquid reservoir is below a predetermined threshold.

Abstract: Disclosed is an auto-injector apparatus for receiving a safety syringe, the safety syringe including a sheath deployable on actuation of a plunger to a position at least partially covering a needle of the syringe, wherein the apparatus is configured to allow movement of the sheath to a closed position that substantially covers the needle.