Abstract: A safety device is described wherein drug delivery systems and methods involve associating unique keys to patients that prevent the interconnection between a drug delivery device and non-complimentary patient key. Medication in a drug delivery device intended for a patient may only be accessed via a particular unique key associated with the intravenous access device of that patient.

Abstract: Described is an autoinjector comprising a case, a needle shroud slidably arranged in the case, a chassis slidably arranged in the case and rotatably coupled to the needle shroud, an outer plunger selectively engaged to the chassis, an inner plunger selectively engaged to the outer plunger, and a drive spring applying a biasing force to the outer plunger. The biasing force is applied to the inner plunger when the inner plunger is engaged to the outer plunger. Axial movement of the needle shroud relative to the case causes rotation of the chassis relative to the needle shroud. The rotation of the chassis causes the inner plunger to rotate relative to the outer plunger and disengage the outer plunger to remove the biasing force from the drive spring on the inner plunger.

Abstract: A peritoneal dialysis system includes: a plurality of automated peritoneal dialysis (“APD”) machines; and a server computer in communication with the APD machines, the APD machines programmed to inform the server computer of how much dialysate is consumed over a first delivery period, the server computer configured to use the amounts consumed to determine dialysate delivery amounts for the plurality of APD machines for a second delivery period.

Abstract: A percutaneous penetration enhancing apparatus includes a sheet member capable of being placed on a skin; a plurality of skin condition sensors arranged on the sheet member, each of the plurality of skin condition sensors detecting information related to a condition of the skin; and a plurality of percutaneous penetration enhancing elements arranged on the sheet member, each of the plurality of percutaneous penetration enhancing elements being operated on the basis of the information detected by one or more of the plurality of skin condition sensors.

Abstract: Disclosed herein is a removable cap for connection to an input port of a catheter, comprising a proximal end having a lumen configured to house a guidewire therethrough; a distal end configured to reversibly mate with a luer lock of the input port of a catheter, the distal end having a lumen configured to house the guidewire therethrough; and a tubular body between the proximal end and the distal end, wherein the tubular body comprises an anti-migration feature transformable between a first configuration to allow slidable movement of the guidewire within the cap in a first direction toward the patient, and a second configuration to prevent slidable movement of the guidewire within the cap in the first direction toward the patient. Systems and methods are also disclosed.

Abstract: A free flow mitigating device for a fluid administration set includes a pump driver mechanism having a locator pin attached and positioned to register with a locator hole on the administration set, for example in a cassette. The locator pin has a surface area. A compressible material is attached to at least a portion of the surface area of the locator pin. The compressible material has a thickness such that it is frictionally received within the locator hole of the cassette sufficient to provide a retaining force to resist cassette movement during closing of a flow regulator valve of the cassette.

Abstract: An injection device for automatically combining two substances, including a body and a cartridge displaceably disposed within the body having a first chamber for containing a first substance, a second chamber for containing a second substance, a first stopper displaceably disposed within the cartridge separating the first and second chambers, a second stopper displaceably disposed within the cartridge defining an end of the second chamber. The device also includes a needle hub displaceably disposed within the body having threads thereon for connecting a pen needle to the injection device. The device additionally includes a plunger displaceably disposed within the body, a biasing member, a sleeve, biased by the biasing member and communicating the bias to the plunger, and an activation button radially displaceable with respect to the body to selectively release the sleeve to drive the plunger and automatically mix the first and second substances.

Abstract: A medicated module for an injection system to co-deliver at least two medicaments is disclosed where a primary delivery device containing a primary medicament accepts a medicated module containing a single dose of a secondary medicament and where both medicaments are delivered through a hollow needle. The medicated module is initially in a locked state until attached to a drug delivery where interaction of the cartridge holder with the module bypass housing changes the module to a triggerable state. The medicated module does not require the user to manually engage a reservoir containing the secondary medicament. Instead, a biasing member automatically activates the reservoir when the needle guard is retracted when the module is in the triggerable state. The needle guard prevents accidental needle sticks before and after an injection, and locks after removal from the injection site.

Abstract: A catheter assembly includes an elongate member and a balloon. The elongate member defines at least one lumen and an outer surface. The outer surface defines at least one opening in fluid communication with the at least one lumen. The balloon is disposed within the at least one lumen. The balloon is inflatable such that a portion of the balloon expands from the at least lumen through the at least one opening. The expansion of the balloon increases the flow restriction through the at least one opening compared to the flow restriction through the at least one opening when the balloon is in a deflated condition. Methods for using a catheter assembly to remove occlusive material from a catheter are also described.

Abstract: Systems for delivery of therapeutic agents and related methods are disclosed. A sensing system is configured to detect a chemical in the vicinity of a patient and transmit a signal to a controller upon detection. A controller is configured to release a therapeutic agent which is transported to the site of interest. The controller communicates with an electronic medical records database, an alarm and a nurse call system.

Abstract: The present invention relates to an injection device (1) having a mechanical dose size display wherein a first scale drum (10) carrying a series of first ciphers (11) and a second scale drum (20) carrying a series of second ciphers (21) are both rotatable able and axially moveable relatively to a housing (2) of the injection device in such a way that one of the first ciphers (11) and one of the a second ciphers (21) appears simultaneously in a window provided in the housing (2) thereby informing the user of the set dose. Both the first scale drum (10) and the second drum (20) preferable carries five ciphers (11, 21) around one full circumferential perimeter. The ciphers (11, 21) are provided in different circumferential circles and/or helically provided.

Abstract: Syringes and methods of using are described which protect the syringe barrel cavity from contaminants. A first syringe is formed with a corrugated sheath which encloses the plunger and space between the rearward end face surface of the syringe barrel handle member and the forward face of the plunger handle member. A second syringe is formed with a syringe barrel having a straight segment and a corrugated segment having the forward face of the plunger handle member molded to the rearward terminus of the corrugated segment of the syringe barrel. A third syringe is formed from mating syringe barrel and plunger member walls. The walls of the mating syringe barrel and plunger member are concentric and slide relative to each other while maintaining an enclosure around the plunger shaft. A fourth syringe is formed from inner and outer concentric syringe barrel walls mating with the walls of a plunger member.

Abstract: An auto-injector comprises a chassis to contain a syringe with a, needle and a stopper, a needle shroud slideable within the chassis and adapted to rest on the skin of a patient, a plunger adapted to translate the stopper to expel medicament, a coupling shroud slideable within the chassis and releasably coupled to the plunger and a drive means, the drive means driving the coupling shroud proximally from a first position Proximal movement of the coupling shroud translates the syringe exposing the needle, depresses the plunger to expel medicament and advances the needle shroud to a safe position to surround the needle. The needle shroud arranged to prevent decoupling of plunger and coupling shroud when the needle shroud is in a retracted position, whereas the needle shroud is arranged to allow decoupling of plunger and coupling shroud when the needle shroud is moved towards the safe position.

Abstract: A connector for coupling to a base of medical device equipped with a circular hub having an annular recess. The connector includes a cap having a top surface, a bottom surface, a circumferential region defining a bottom plane and a periphery, and at least two arms substantially parallel to the bottom plane. Each arm spans at least two portions within the circumferential region to releasably engage the annular recess. At least one deflection member that is accessible from the top surface is positioned to deflect the arms. Pressing the connector onto the circular hub engages the arms with the annular recess so the connector can rotate completely about the circular hub. Pressing at least one deflection member to reversibly deflect at least one arm between its two portions of the circumferential region towards the periphery disengages the arm from the annular recess to decouple the connector.

Abstract: The invention refers to an auto-injector comprising: a body, a syringe with a hollow injection needle and a stopper, wherein the syringe is slidably arranged with respect to the body, a torsion spring capable of, upon activation: pushing the needle from a covered position inside the body into an advanced position through the orifice and past the proximal end (P), operating the syringe to supply the dose of medicament (M), and activating means arranged to lock the spring means in a pressurized state prior to manual operation and capable of, upon manual operation, releasing the spring means for injection, wherein the torsion spring is grounded at one end in the body and at the other end in a first gear member rotatable about a longitudinal axis, wherein the first gear member, upon rotation, is arranged for translating a second gear member toward the proximal end (P), the second gear member prevented from rotating and arranged to be coupled to the stopper in order to push it towards the proximal end (P), wher

Abstract: An aspect of some embodiments of the current application is a doorstop to a drug delivery apparatus that encourages a user of the apparatus to perform the proper usage steps in the proper order. For example, a user may be expected to receive an injector in a transport state, open it to an open state, insert a cartridge, and/or close the cartridge before operation. The doorstop may have an obstructing mode, optionally preventing closing of the door. The cartridge may optionally have a non-obstructing mode allowing closing of the door. Inserting the cartridge may optionally cause a doorstop to move from the obstructing mode to the non-obstructing mode. In the non-obstructing mode the doorstop may optionally prevent removal of the cartridge.

Abstract: A medical device that automates protocol compliance by performing one or more of measuring relevant data, determining dosage, dispensing appropriate dosages, ordering supplies, updating protocol, contacting third-parties, logging events, and reporting data.

Abstract: The tamper evident cap assembly is structured for protective connection to a syringe of the type having a nozzle and a discharge port, wherein the cap assembly includes a body configured to receive and restrict access to the nozzle. A flow restricting member is connected to the body in flow restricting relation to the discharge port of the nozzle. An attachment assembly interconnects the body and the flow restricting member and is structured to facilitate detachment of the body from the flow restricting member upon the body being removed from the syringe. A connecting assembly is mounted on the flow restricting member and is structured to be connected to a syringe nozzle by a linearly directed, snap-fit, “push-on” action, and to be disconnected therefrom by a “rotate-off” action.

Abstract: The invention relates to a device for drug administration and/or monitoring the status of a patient, the device comprising a first and a second measuring means, and the time for using the second measuring means being set in accordance with the data of the first measuring means.

Abstract: Needle assemblies are generally discussed herein with particular discussions extended to needle assemblies having a tip protector with a plurality of wall surfaces for preventing contact with the needle tip from a side. Aspects of the tip protectors discussed herein include a first protector body having an arm for blocking a needle tip surrounded by a second protector body having a plurality of wall surfaces.