Abstract: A system comprising a device and a monitoring unit configured to monitor the mechanical health of the device is disclosed. The monitoring unit may comprise at least one actuator, at least one sensor and at least one processing resource. The at least one actuator may be configured to vibrate the device and the at least one sensor may be configured to detect a corresponding output of the device. The at least one processing resource may be configured to process the output detected by the at least one sensor and to assess the mechanical health of the device by comparing the detected output of the device to a healthy fingerprint of the device, wherein the healthy fingerprint is an output of the particular device being tested when it is free of mechanical defects.

Abstract: An automatic injection device has an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product and includes a plunger. The automatic injection device also has a fluid path which fluidly connects the drug container to the insertion needle, and a drive system configured to cause linear movement of the plunger to force the pharmaceutical product into the fluid path. The passive drive system has a movable element. The movable element has a shape memory alloy and is configured to change shape to move the plunger.

Abstract: A system and method for calibrating an IV pump infusion system tube comprises a fluid source, an infusion system comprising, an IV pump, a drive unit, a chamber with known constant volume, a control unit, and IV tubing with a known inner diameter tolerance, and a switch and magnetic floating object. The system administers medicinal fluid, calculates the flow rate of the medicinal fluid in the chamber by measuring the time the switch is activated as medicinal fluid rises in the chamber, compares the calculated flow rate with a set flow rate of the IV pump input in the control unit prior to infusion, and adjusts the IV pump and flow rate based on the compared deviations for more accurate delivery to a patient. This configuration may provide a more precise delivery rate of medicinal fluid, preventing harm to the patient and waste of medicine.

Abstract: A system and method for calibrating an IV pump infusion system tube comprises a fluid source, an infusion system comprising, an IV pump, a drive unit, a chamber with known constant volume, a control unit, and IV tubing with a known inner diameter tolerance, and a set of conductive plates. The system administers medicinal fluid, calculates the flow rate of the medicinal fluid in the chamber by measuring the time the capacitance level of the medicinal fluid changes from a capacitance level corresponding to a first (initial) position to a capacitance level corresponding to a second (filled) position, compares the calculated flow rate with a set flow rate of the IV pump input in the control unit prior to infusion, and adjusts the IV pump and flow rate based on the compared deviations for more accurate delivery to a patient. This configuration may therefore provide a more precise delivery rate.

Abstract: A system and method for calibrating an IV pump infusion system tube comprises a fluid source, an infusion system comprising, an IV pump, a drive unit, a chamber with known constant volume, a control unit, and IV tubing with a known inner diameter tolerance, and a sensor and floating detection object. The system administers medicinal fluid, calculates the flow rate of the medicinal fluid in the chamber by measuring the time the floating detection object and medicinal fluid rises in the chamber, compares the calculated flow rate with a set flow rate of the IV pump input in the control unit prior to infusion, and adjusts the IV pump and flow rate based on the compared deviations for more accurate delivery to a patient. This configuration may provide a more precise delivery rate of medicinal fluid, preventing harm to the patient and waste of medicine.

Abstract: An apparatus and method for the aseptic delivery of a solution in a wearable form factor is disclosed. A patch pump may include a start button that, upon activation, causes an elastic fluid path to move. The elastic fluid path may include a first end that moves along a first plane to penetrate a solution container as well as a second end that moves, concurrently, along a second plane to penetrate a user's tissue. The elastic fluid path may maintain its flow resistance during the concurrent movement. The patch pump's housing may include a door with an opening configured to enable the second end to penetrate a user via the opening. The door may open when the device is removed from the user such that a portion of the open door may extend further than the second end of the elastic fluid path to prevent exposure of the second end.

Abstract: A device and method for cannula insertion into a users tissue are disclosed. A patch pump comprising a non-linear needle path with a first bend may be provided. A rigid needle may be located in the needle path and may be composed of a material that allows the rigid needle to maintain a bend at the first bend when traversing the non-linear needle path. A movement mechanism may be configured to apply force on a first end of the rigid needle to cause the rigid needle to traverse the non-linear needle path from a first needle position to a second needle position. A cannula may receive a force from a second end of the rigid needle when the movement mechanism applies the force on the first end of the rigid needle and configured to traverse from a first cannula position to a second cannula position based on the force.

Abstract: A device and method is disclosed for assembling a container holder in a clean environment, aseptically adding a solution to a primary container, inserting the primary container into the container holder, applying a first barrier to the container holder, sterilizing the container holder comprising the primary container and the applied first barrier to provide a sterilized container holder, assembling a fluid path module in a clean environment, the assembling comprising applying a second barrier to a first end of the sterilized fluid path module, sterilizing the fluid path module to provide a sterilized fluid path module and assembling a delivery device comprising the sterilized container holder and the sterilized fluid path module.

Abstract: A device and method for creating a fluid path are disclosed. A patch pump may include a start button. A force may be applied on a button needle in a force direction, based on activating the start button. A first end of the button needle may puncture a fluid container by moving the button needle from a first button needle position to a second button needle position via the force in the force direction. A second end of the button needle may be positioned underneath a carrier septum contained in a carrier, via the applied force. The carrier may be released based on activating the start button and the second end of the button needle, based on releasing the carrier, may puncture the carrier septum. A fluid path may be provided form the fluid container to a patient's tissue based on puncturing the fluid container and the carrier septum.

Abstract: A device and method are disclosed for an elastic strip with a first fixed end and a second movable end, the elastic strip configured to be in at least one of a tense state and an elastic state. A release mechanism is configured to maintain the elastic strip in a tense state when the release mechanism is in a holding state, and configured to release the elastic strip when in a release state. A needle path with a first bend is provided. A rigid needle is configured to traverse a first portion of the needle path when the elastic strip is in the elastic state and a cannula is located in the needle path and configured to traverse a second portion of the needle path when the rigid needle traverses the first portion of the needle path.

Abstract: An automatic injection device with flow regulation. The automatic injection device has an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product and includes a plunger. The automatic injection device also has a fluid path which fluidly connects the drug container to the patient via an insertion device, a potential energy source, and a regulator configured to restrict release of potential energy and restrict linear movement of the plunger and pharmaceutical product into the fluid path at a proscribed pace. The regulator includes a clock escapement mechanism. The potential energy source may be a spring that surrounds the drug container and may be magnetically coupled to the plunger. The clock escapement mechanism is configured to control the spring at a regulated rate over a time interval using a gearbox and rotational-to-linear translator comprising a rack and pinion.

Abstract: An automatic injection device with flow regulation. The automatic injection device has an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product and includes a plunger. The automatic injection device also has a fluid path which fluidly connects the drug container to the patient via an insertion device, a potential energy source, and a regulator configured to restrict release of potential energy and restrict linear movement of the plunger and pharmaceutical product into the fluid path at a proscribed pace. The regulator includes a clock escapement mechanism and a wire and pulley system including a wire coupled to at least one pulley. The potential energy source may be a spring that surrounds the drug container and may be directly coupled to the plunger and the wire such that movement of the spring and the wire is restricted over time.

Abstract: A device and method for measuring an IV pump infusion system flow comprises a fluid source configured to store medicinal fluid and a weight sensing mechanism comprising a weight sensor and microprocessor. The weight sensing mechanism is configured to detect the weight of the fluid source as the medicinal fluid leaves the fluid source. The device in the infusion system administers medicinal fluid using a set flow rate for the IV pump input into the control unit prior to infusion, measures the change in mass of the fluid source containing medicinal fluid as fluid exits the source, calculates the flow rate based on the change in mass over time, compares the calculations with a set flow rate, and adjusts the IV pump and flow rate based on the compared deviations, for improved delivery accuracy. This configuration may also prevent patient harm and medicine waste.

Abstract: An automatic injection device has an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product. The drug container includes a stopper. The automatic injection device also has a fluid path which fluidly connects the drug container to the insertion needle. The automatic injection device further has a drive system configured to cause parallel linear movement of the stopper to force the pharmaceutical product into the fluid path. The drive system has a driving element and a movable element. The automatic injection device additionally has electronics configured to provide a signal to the drive system to move the stopper and have means for sensing the stopper position. The movable element has an outer magnet at least partially surrounding the drug container and an inner magnet inside the drug container.

Abstract: An automatic injection device has an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product and includes a plunger. The automatic injection device also has a fluid path which fluidly connects the drug container to the insertion needle, and a drive system configured to cause linear movement of the plunger to force the pharmaceutical product into the fluid path. The drive system has a movable element. The movable element has a shape memory alloy and is configured to change shape to move the plunger.

Abstract: An automatic injection device has an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product. The drug container includes a plunger. The automatic injection device also has a fluid path which fluidly connects the drug container to the insertion needle. The automatic injection device further has a drive system configured to cause linear movement of the plunger to force the pharmaceutical product into the fluid path. The drive system has a driving element and a movable element. The automatic injection device additionally has electronics configured to provide a signal to the drive system to move the plunger. The movable element has an outer magnet at least partially surrounding the drug container and an inner magnet inside the drug container.

Abstract: A lancing device (e.g., pen) having an integrated thermoelectric (e.g., Peltier) cooler. The lancing device includes an elongated heat accumulator having a lumen along which a piston having a lancet thereon translates back and forth. A Peltier device and a cooling ring are thermally interconnected to one end of the heat accumulator and include central apertures through which the lancet can extend. The lancing device also includes an integrated battery and microcontroller for supplying and regulating power to the Peltier device. Upon a current being sent through the Peltier device, a cold side of the Peltier device and hence the cooling ring gives up thermal energy and reduces in temperature. The cooling ring can then be placed about a body tissue (e.g., skin) for a period of time (e.g., 3-5 seconds) to desensitize the body tissue, and then the lancet can be fired to puncture the body tissue.

Abstract: A metered dose inhaler with an electronic dose counter, and method of operating and forming the same. In one embodiment, the metered dose inhaler includes a pressurized canister assembly formed with a memory device affixed thereto. The metered dose inhaler also includes a canister housing into which the pressurized canister assembly is inserted, the canister housing formed with an electronic dose counter including a display configured to display a dose count of a drug in the pressurized canister assembly stored in the memory device.

Abstract: A system including a host device and a measurement device ultrasonically coupled to the host device over a physical medium and method of operating the same has been introduced herein. In one embodiment, the system includes the host device including a first ultrasonic communicator configured to generate an ultrasonic command to measure a parameter of an object, a physical medium coupled to the host device and the measurement device coupled to the physical medium. The measurement device includes a second ultrasonic communicator configured to receive the ultrasonic command via the physical medium, and a sensor configured to measure a parameter of the object in response to the ultrasonic command to provide a sensed parameter, the second ultrasonic communicator being configured to transmit the sensed parameter to the host device via the physical medium.

Abstract: A technique for making an RFID tag that includes creating recesses or trenches in an insulated substrate. Conductive traces are created in the trenches so as to create an inductor coil for the RFID tag.