A system for confirming acquisition of a fluid sample is provided. The system includes a wearable electronic device configured to be worn by a user. The device has a housing, at least one imaging sensor associated with the housing, a data transmission interface for sending data to or receiving data from an external electronic device, a microprocessor for managing the at least one imaging sensor and the data transmission interface, and a program for acquiring and processing images acquired by the at least one imaging sensor. The system further includes a sampling device for collecting a fluid sample in a sample container and at least one identification tag attached to or integrally formed with the sampling device or sample container. The at least one identification tag includes or is associated with a tracking code.

An apparatus includes a housing, defining an inner volume, and an actuator mechanism movably disposed therein. The actuator mechanism is configured to be transitioned from a first configuration to a second configuration to define a pre-sample reservoir fluidically couplable to receive a pre-sample volume of bodily-fluid via an inlet port of the housing. The actuator mechanism is movable from a first position to a second position within the housing after the pre-sample reservoir receives the pre-sample volume such that the housing and the actuator mechanism collectively define a sample reservoir to receive a sample volume of bodily-fluid via the inlet port. The outlet port is in fluid communication with the sample reservoir and is configured to be fluidically coupled to an external fluid reservoir after the sample volume is disposed in the sample reservoir to transfer at least a portion of the sample volume into the external fluid reservoir.

Fill stations and base stations are provided for personal pump systems. The fill stations may be opened and closed to accept a reservoir and to allow fluid to be introduced into the reservoir for use with personal pump systems. The fill stations may hold the reservoir at a tilt relative to an underlying surface and may discourage overfilling of the reservoir. The filling stations may also include viewing windows having fluid lines marked thereon for indicating volume of fluid within the reservoir.

A transfer device includes an introducer coupleable to a peripheral intravenous catheter, with the introducer having a proximal end portion and a distal end portion, a catheter having a proximal end portion and a distal end portion and defining a lumen, a secondary catheter having a proximal end portion and a distal end portion and defining a lumen, and an actuator receiving the proximal end portion of the catheter and the distal end portion of the secondary catheter. The actuator is moveable within introducer from a first position where the distal end portion of the catheter is positioned within the introducer to a second position where the distal end portion of the catheter is positioned outside of the introducer.

A cannula insertion system for inserting a cannula into a human or animal body, includes a cannula and a cannula insertion device to hold and insert the cannula into the human or animal body in an insertion direction. The cannula insertion system includes a safety device configured to retract the cannula or to release the cannula from the cannula insertion device when a force exerted on the cannula in a direction perpendicular to the insertion direction results in exceeding a respective safety threshold value.

A capillary chamber for performing chemical and physical analysis using a plurality of whole blood samples is presented. Following a loading of the whole blood samples into a plastic tube, the whole blood samples are distributed into a collection chamber and the capillary chamber has means of adding respective vaccines or similar biological products into each capillary tubes. The whole blood is then analyzed using standard microscopic techniques with sufficient resolution and contrast to record the chemical and physical properties of the blood immediately after withdrawal.

An integrated intravenous catheter including a catheter adapter having a catheter and an inlet, the catheter configured to be inserted into a patient's vasculature, as well as a needle free connector. The needle free connector includes first port, a second port positioned opposite the first port, and a side port positioned between the first port and the second port. The needle free connector further includes a main cavity portion having a tapered sidewall and a distal taper portion, wherein the tapered sidewall gradually narrows in a direction of the distal taper portion. The integrated intravenous catheter also includes intermediate tubing extending between the inlet of the catheter adapter and the first port of the needle free connector, and extension tubing extending from the side port of the needle free connector.

A system is disclosed. The system includes a reservoir for containing a fluidic medium, the reservoir including a front surface, a resilient cylindrical flexure portion connected to the front surface, the resilient cylindrical flexure portion comprising an accordion-like structure that is able to expand and contract to change an interior volume within the resilient cylindrical flexure portion, a central passageway within the resilient cylindrical flexure, and a collection chamber connected to the central passageway. Also, a system including a reservoir, a plunger head located within the reservoir, a plunger arm connected to the plunger head, a driving shaft connected to the plunger arm, and a motor connected to the driving shaft, the motor controllable to move the drive shaft in a first motion and a second motion so as to move the advance plunger head and retract the plunger head within the reservoir.

A cannula insertion system for inserting a cannula into a human or animal body, includes a cannula and a cannula insertion device to hold and insert the cannula into the human or animal body in an insertion direction. The cannula insertion system includes a safety device configured to retract the cannula or to release the cannula from the cannula insertion device when a force exerted on the cannula in a direction perpendicular

Disclosed is a syringe apparatus. Syringe apparatus has a barrel including an inner surface, an open end, and an inlet end; a plunger including a plunger head received in slidable sealing contact with the inner surface of the barrel and forming a reservoir therein; and an extensible member, optionally including an additive, is contained in the reservoir. Extensible member can be coupled between the inlet end and the plunger head and is extensible in length L as a bio-liquid (e.g., whole blood) is drawn into the reservoir. Methods of mixing or adding an additive such as an anticoagulant, coagulant, or marker, to a bio-liquid are provided, as are other aspects.