This invention pertains to systems and components useful for infusing medications such as insulin. Typically, the components are used to deliver insulin to a diabetic patient at a site of infusion over a period of time greater than 4 days. The system components typically comprise a cannula adapted for subcutaneous insertion into a diabetic patient. The system further comprises a fluid conduit adapted to deliver the insulin solution from a medication reservoir to the site of infusion and a depot in operable contact with the fluid conduit. The depot comprises selected materials including a site-loss mitigating agent (such as heparin) which inhibits inflammation at the site of infusion, and encapsulation of the cannula at the site of infusion. The site-loss mitigating agent is not premixed with the insulin, and instead is adapted to contact the insulin solution in the depot as the insulin solution flows from the medication reservoir to the site of infusion.

Some embodiments of an infusion pump system may be configured to wirelessly communicate with other devices using near field communication (NFC). In particular embodiments, by incorporating near field communication capabilities into the infusion pump system, user communications with the infusion pump system can be enhanced and simplified.

A stabilizing connector includes a connector portion and a stabilization portion. The connector portion is configured to couple to an access device. The connector portion defines at least one lumen that is configured to be placed in fluid communication with a lumen of the access device. The stabilization portion is coupled to the connector portion. The stabilization portion is configured to be placed in contact with a surface of a patient's skin to stabilize at least one of the stabilizing connector or the access device.

A system for delivering a fluid to tissue and a method of using same are provided. The system includes a tissue clip for securing a tissue fold and a tissue puncturing device attachable to the tissue clip. The system further includes a mechanism for sensing the tissue fold and releasing a safety mechanism in the tissue puncturing device so as to enable manual deployment of a tissue puncturing element from the tissue puncturing device.

An intravenous cuff assembly includes a cuff that is wearable around a user's arm to cover an injection site of an intravenous needle. The cuff is comprised of a resiliently stretchable material to compress against the intravenous needle thereby inhibiting movement of the intravenous needle. A plurality of first mating members and a plurality of second mating members is each coupled to the cuff. Each of the second mating members is releasably matable to a respective one of the first mating members for adjusting dimensions of the cuff. A plurality of third mating members and a plurality of fourth mating members is each coupled to the cuff. Each of the fourth mating members is releasably matable to a respective one of the third mating members for adjusting dimensions of the cuff.

Systems and methods for delivering a medication to a person experiencing an emergency medical event without requiring intervention or action on the part of the person. A device encases a reservoir of medication and a delivery mechanism. Sensors in the housing sense a physical attribute of the person and circuitry monitors information collected by the sensors to determine if the person is experiencing a severe medical condition or event based on the information. An input device on or in the housing, such as a button, may be used or activated by the person if the detected condition or event is a false positive to cancel further action. If the system does not include the button or if the user does not press it in time, the system activates the delivery device and injects the medication into the person.

In some embodiments, an apparatus may comprise a first insertion needle and a second insertion needle. The first insertion needle may be configured to carry a first medical device (e.g., a sensor) through an opening in an apparatus housing. The second insertion needle may be configured to carry a second medical device (e.g., a cannula) along a curved path that passes through the opening in the apparatus housing such that a distal end of the first medical device becomes increasingly displaced from the distal end of the second medical device as the distal end of the second medical device is carried along the curved path.

An intravenous (IV) catheter system may include a catheter adapter having a proximal end and a distal end. The IV catheter system may also include a cannula extending through the catheter adapter. A proximal end of the cannula may include a notch. The IV catheter system may also include a needle hub, which may be coupled to the proximal end of the catheter adapter. The needle hub may include a flashback chamber, which may be in fluid communication with the notch when the IV catheter system is in an insertion configuration.

A medicament delivery device may comprise a medicament chamber configured to hold a medicament, a plunger configured to move relative to the medicament chamber to expel the medicament from the medicament chamber, a pin configured to move from a first pin position wherein the pin prevents movement of the plunger to a second pin position wherein the pin allows movement of the plunger, an actuation assembly configured to move the pin from the first pin position to the second pin position, and a needle coupled to the medicament chamber. The medicament may flow through the needle from the medicament chamber to a user. The actuation assembly may be configured to automatically move the pin after a predetermined time delay.

An activation mechanism for an on-body medicament delivery device, wherein the activation mechanism comprises: an activation button structure configured to be moved between an initial position and an activation position, an activation pin sleeve, and a biased activation pin received by the activation pin sleeve, the activation pin being configured to be linearly movable from an initial retracted position relative to the activation pin sleeve to an extended position towards which the activation pin is biased, the activation button structure being configured to interact with the activation pin sleeve in the initial position to cause the activation pin sleeve to engage with and maintain the activation pin in the retracted position, and wherein the activation button structure is configured to interact with the activation pin sleeve when the activation button structure is moved linearly towards the activation position causing the activation pin sleeve to release the activation pin from the retracted position.