An assembly for forming an injection device, comprising: a foot to be placed on a skin; a body comprising at least one needle, the body being movably mounted to the foot for allowing movement of the needle towards the skin, the needle extending out of a second contact surface by a predefined distance for limiting a penetration depth of the needle; first friction means for preventing movement of the body relative to the foot for causing a sudden acceleration; the assembly further comprising second friction means for creating a dynamic friction when the needle is moving towards the skin for keeping the skin stretched.

A dose recording device (100) for a drug delivery device is disclosed, wherein the drug delivery device comprises a housing, a cartridge holder configured to receive a cartridge for holding a plurality of doses of a drug, and a dose setting member connected to the housing and configured to set the dose of the drug. The dose recording device (100) comprises a device housing (102), an electronic controller (114) disposed within the device housing (102), and at least one identifier member (120) configured to be mounted to the device housing (102). The electronic controller (114) comprises switches (116). The identifier member (120) comprises at least one actuation member (122) configured to actuate at least one of the switches (116) when mounted to the device housing (102). An actuation of the switch (116) is configured to provide additional information on the drug.

Embodiments described herein generally relate to devices, systems and methods for measuring a volume or number of doses remaining in a drug delivery device that is used for delivering a dose to a patient. In some embodiments, a dose measurement system for measuring the liquid volume in a container includes a light guide disposed and configured to reflect electromagnetic radiation toward the container. The dose measurement system also includes a light guide disposed and configured to emit electromagnetic radiation into the light guide. A plurality of sensors are located in the apparatus that are optically coupleable to the light guide and are disposed and configured to detect the electromagnetic radiation emitted by at least a portion of the light guide. The apparatus also includes a processing unit configured to receive data representing the portion of the detected electromagnetic radiation from each of the plurality of sensors. The processing unit is further operable to convert the received data into a signature representative of the electromagnetic radiation detected by the plurality of sensors.

A system for delivering an injection of a fluid into a void within a subject is disclosed. A barrel extends from a first end to a second end and forms a lumen extending from the first end to the second end. A plug and a floating seal are arranged within the lumen. A hollow needle includes a distal end with an opening for fluid to flow from the lumen. The plug, the barrel and the floating seal include material and dimensions selected based on a threshold flowrate for a fluid arranged within the lumen to: overcome a force opposed to a force being applied to the fluid in the lumen to move the floating seal and the hollow needle into a tissue of the subject, and succumb to the opposing force to displace the fluid through the opening into the void.

A stopper being adapted to be fixed in a rear end portion of a syringe is provided. The stopper is reduced in diameter at a fitting portion of a rod portion of a plunger rod so as to have a diameter smaller than an inner diameter of the rear end portion and be insertable into the rear end portion. After insertion, the stopper is increased in diameter and is fixed in the rear end portion so as not to be movable in an axial direction by fitting a first recessed portion on a periphery into a second protruding portion of an inner surface of the rear end portion. The stopper has, on an inner surface, a third protruding portion having an inner diameter smaller than an outer diameter of a gasket support flange of the rod portion in a fixed state.

A smart vial adapter is capable of measuring the dose of a drug that is withdrawn from a vial, measuring the time of a dose capture event, monitoring the vial temperature, measuring the amount of motion or perturbation the vial is subjected to, capturing various other parameters that can provide additional insights associated with the drug or the amount of the dose being drawn from the vial, and communicating the recorded information to a companion application on a computer, smartphone or other device. Related methods are also disclosed and claimed.

A user-operated apparatus comprising of a body which holds a Raulerson syringe and contains a trigger mechanism to pull the plunger end of the Raulerson syringe to aspirate contents, all of which can be held and controlled with a single hand, and a mechanism housing a controller board, electrical circuit, and gears that allows for loading the guide wire into the Raulerson syringe.

A medical device (1) for administering a medical fluid to a patient (4) comprises a housing (10) comprising a housing portion (11), a control device (19) for controlling operation of the medical device (1), a control element (18) placed on said housing portion (11) and being actuatable for entering a control command to be input to the control device (119), wherein the control element (18), for actuation, is at least one of rotatable about an axis of rotation (R) and linearly movable along the axis of rotation (R) with respect to said housing portion (11), and an actuation element (15) operatively connected to the control element (18) for actuating the control element (18). Herein, the actuation element (15) comprises a first knob element (17) operatively connected to the control element (18) and a second knob element (16) supported on said housing portion (11).

A syringe use monitoring device that can attach to a syringe and detect the type of medication being loaded and measure the force applied to the plunger and thus monitor subsequent delivery of medication and delivery pressure as a substance is being injected, and at least one display and/or alarm can indicate normal and/or abnormal conditions so that feedback can be employed during the injection process is provided.

Embodiments of the invention include a medicament device configured to provide stepwise instructions for using the device to a user in a particular sequence is provided. The device includes a device housing configured to receive a container, the housing including a control interface, the control interface including at least one responsive member reactive to a user input, an actuation mechanism configured to interact with the container, a signal output component associated with the device housing, and circuitry associated with the device housing configured to control a provision of the stepwise instructions to the user in the particular sequence. The container includes a first housing for containing a medicament, a second housing, and an injection member, wherein the first and second housings are movable relative to one another. The container further includes an injection member which is retractable within the second housing to prevent an unintentional contact with the injection member.