The present invention relates to drug delivery systems that cannot be reloaded or reused and further include a passive safety shield system. The drug delivery devices described herein include a drug container comprising at least one bellow, a needle, wherein the needle is in liquid communication with the drug container; a plunger extending between a proximal end and a distal end, wherein the plunger is in communication with the drug container and where upon axial movement of the plunger, the drug container is compressed.

An antimicrobial cap and method for inhibiting the growth of microbes and disinfecting a port are disclosed. The antimicrobial cap comprises an assembly that includes an outer cap, an inner component and a pad disposed within the inner component and impregnated with an antimicrobial element in order to disinfect the port. The antimicrobial cap includes flexible attachment features configured to engage a port and a lockout mechanism configured to prevent and disable re-use of the cap, allowing the disinfection of different types of ports and connectors and safe disengagement of a single-use cap.

An antimicrobial cap and method for inhibiting the growth of microbes and disinfecting a port are disclosed. The antimicrobial cap comprises an assembly that includes an outer cap, an inner member and a pad disposed within the inner member and impregnated with an antimicrobial agent in order to disinfect the port. The antimicrobial cap includes attachment features and a lock out mechanism allowing the disinfection of different types of ports and connectors and their safe disengagement and thereafter enabling the lock out mechanism in order to prevent re-use of the antimicrobial cap.

In an elongated casing, an active agent container connected to an injection needle can be shifted axially by a spring force. Auto-injectors distributed pre-filled and with the springs tensed may be provided with a needle protecting cap to ensure sterility of the needle. When the needle protecting cap is removed as preparation for using the auto-injector, a tensile force can be exerted on the active agent container. Therefore, the active agent container and needle must be prevented from being undesirably pulled forwards. At least one latching tongue prevents the active agent container from being prematurely shifted with respect to the casing, by abutting a flange arranged on a sliding sleeve accommodating the active agent container. When the auto-injector is placed onto the skin, a needle protecting tube is shifted into the casing, forcing the latching tongue away from the flange, thereby freeing the travel path for needle movement.

The present invention provides disposable capsules and electronic inhalers designed to be used therewith, and to methods for consuming cannabis in a clean, simple and efficient way, which is also cost effective.

A medical fluid delivery system includes: a medical fluid delivery machine including a component having at least one of associated output data or associated test data; at least one of a (i) component output replacement limit and a component output soft limit for the component or (ii) a component testing replacement limit or a component testing soft limit for the component; and a computer programmed to store at least one of (i) or (ii), and for (i) analyze the output data to provide a first indication of how well the component is performing relative to the component output replacement limit and the component output soft limit, and for (ii) analyze the test data to provide a second indication of how well the at least one component is testing relative to the component testing replacement limit and the component testing soft limit.

A system may include a disposable flow sensor and a base for the disposable flow sensor. A method may include scanning, with an optical scanner of the base for the disposable flow sensor, a flow sensor label attached to the disposable flow sensor to decode a flow sensor identifier associated with the flow sensor, scanning, with the optical scanner of the base for the disposable flow sensor, a patient label attached to a patient to decode a patient identifier associated with the patient, and connecting the disposable flow sensor to the base.

A catheter drainage bag assembly, a urine-collecting device, and a disposable, portable urine drainage kit is provided. The assembly includes a tube, a drainage bag, and a connector. The tube is secured to a mouth of the drainage bag by way of the connector. The urine-collecting device includes a foldable waterproof pouch with an inlet, a tubular reinforcement; and a connector connecting the inlet of the foldable waterproof pouch to the tubular reinforcement. The disposable, portable urine drainage kit includes at least one tube, at least one connector, and at least one urine drainage bag with a mouth that secures to the tube with the connector.

This invention relates to a humidification assembly or kit for use in a respiratory support system for delivering humidified gas to a user or patient. The assembly or kit comprises a fluid reservoir, and a humidification chamber. The fluid reservoir and the humidification chamber are provided in fluid connection with each other, wherein a connection between each of the fluid reservoir and the humidification chamber provides a pre-determined force of retention and/or resistance to disconnection or is a permanent type connection.

Pre-filled syringes include an elastic and sliding valvular joint acting as a temporary closure to prevent internal chamber(s) from communicating with the outside (or between chambers). The joint includes two discoid cooperative elements: an elastic discoid cap and a sliding receiving discoid seat that has a central passage tube. The cap includes an elastic base from which a compact closing cylinder protrudes. The closing cylinder has a distal area with a plurality of longitudinal grooves. The cap can: (a) half-fit the central tube of the receiving discoid seat, which will allow the communication of fluid through the plurality of grooves, and (b) seal the chamber by completely fitting the central tube of the receiving discoid seat. Accordingly, the half-fit position allows the lyophilization of contents of the syringe.