A sensor assembly may include a sensor surrounding a connector of a medical device. The sensor may be configured to detect a dimension of an end of another connector of another medical device when the another connector of the another medical device is connected to the connector of the medical device. A system may include the sensor assembly and one or more processors programmed and/or configured to determine a type of the another medical device based on the detected dimension. A method may include detecting, with a sensor surrounding a connector of a medical device, a dimension of an end of another connector of another medical device when the another connector of the another medical device is connected to the connector of the medical device; and determining a type of the another medical device based on the detected dimension.

Cartridges are configurable between a closed state and an open state. The cartridges include a cartridge body and a reservoir disposed in the cartridge body. The cartridge body has an outer locking element, and the reservoir has a rotational locking element. In the closed state, the outer locking element engages the rotational locking element such that the reservoir cannot be rotated out of a first rotational position relative to the cartridge body in which a fluid outlet of the reservoir is not in fluid communication with a fluid outlet of the cartridge body. In the open state, the outer locking element of the cartridge body does not engage the rotational locking element of the reservoir, and the reservoir is in a second rotational position relative to the cartridge body such that the fluid outlet of the reservoir is in fluid communication with the fluid outlet of the cartridge body.

A filter adaptor includes a body that defines an internal passageway disposed between an inlet and an outlet, the passageway configured to permit passage of a fluid in a first direction defined by the inlet and the outlet; and a filter disposed within the passageway and oriented to define a volumetric direction that is different than the first direction. Another filter adaptor includes a body that defines an internal passageway disposed between an inlet and an outlet, and a filter disposed within the passageway, wherein the filter comprises a gelling absorbent material that, when in a dry state, is permeable to gas and that, when contacted by an aqueous fluid, converts to a gel. Such filter adaptors may be used for negative pressure wound therapy, dressing, or as syringe filters.

In one embodiment, an integrated cannula and sensor assembly is disclosed. The integrated cannula and sensor assembly includes a cannula with a proximal end and a distal end. The cannula also has a body and a tip. The body includes a channel and a body distal that is defined between the proximal end and the distal end. The tip is defined between the body distal and the distal end. The assembly further includes a sensor assembly that is located within the channel, wherein the tip further includes an undercut configured to retain the sensor assembly.

An apparatus includes a movable member and a valve coupled to the movable member. The movable member is configured to be disposed within a housing of a medical device and has a first end portion and second end portion. A portion of the first end portion is configured to define a portion of a boundary of a gas chamber. The first end portion defines an opening configured to be in fluid communication between the gas chamber and an area outside the gas chamber. The second end portion is configured to be coupled to a needle configured to deliver a medicament into a body. The valve is configured to selectively allow fluid communication between the gas chamber and the area outside the gas chamber through the opening defined by the first end portion of the movable member.

An autoinjector apparatus is disclosed which comprises a single-use cassette and an autoinjector. The cassette comprises a housing and a sleeve movably disposed in the housing. A syringe may be disposed in the sleeve and secured therein with a lock cap. The lock cap is affixed to a distal end of the sleeve and contacts the distal end of the syringe. A shield remover extends through an opening in a proximal end of the housing for removing a needle shield which covers a needle of the syringe. A cassette identification arrangement is provided on a surface of the housing to enable the autoinjector to identify the cassette. The autoinjector is provided with a detector for reading the cassette identification arrangement.

A cassette for use with an injector has a housing, and a cassette identification arrangement (cassette ID) defining a code containing information about the cassette that is detectable and decipherable by an injector. The cassette may further have a sleeve movably disposed within the housing, for holding a drug container, and a locking arrangement for interlocking the sleeve with the housing. The cassette may further have an aperture in the housing, and a cassette cap for removing a needle shield of the drug container. The cassette may have an anti-bending structure to prevent bending or flexing of the cassette cap. The injector may have a processor for controlling operational parameters of the injector and a detector communicatively coupled with the processor for detesting and communicating the cassette ID to the microprocessor to decipher the code defined therein. Also, a method of injecting a drug into a patient with an injector, wherein the sequence of actions performed by the user are controlled. Still further, a method of treating a patient in need thereof wherein a cassette containing a drug is provided and administered to the patient using an injector.

Cartridges have a cartridge body configured to store a formulation, a formulation valve disposed in the cartridge body, and an air valve disposed in the cartridge body. The cartridge is configured to dispense the formulation through the formulation valve when the formulation valve and the air valve are each in an open state, and to not dispense the formulation when the formulation valve and the air valve are in a closed state.

A transfer device can include a housing including first and second docking cups, each of the first and second docking cups configured to receive and lockably engage a receiver of a transfer system; a security mechanism positioned inside the housing, the security mechanism including: first and second security levers; a first biasing member engaged with the first security lever and configured to bias the first security lever towards engagement with the receiver; and a second biasing member engaged with the second security lever and configured to bias the second security lever towards engagement with the receiver; and an indicator coupled to the security mechanism and at least partially visible from outside the housing, the indicator configured to indicate to a user of the transfer system whether the receiver is lockably engaged with one of the first and second docking cups.

A multi-medicament infusion system (10) for preventing the mischanneling of medicaments may include an infusion pump (12), medicament reservoirs (16A,16B), a multi-channel lumen (18), and an infusion set (20). The medicament reservoirs may be sized and shaped differently such that the medicament reservoirs can only be inserted into the infusion pump in a unique configuration. The multi-channel lumen may include connectors that mate to corresponding connectors on the infusion pump and the infusion set only in a unique configuration. Because the various parts of the multi-infusion system may only be connected in the unique configuration, the expected medicaments may be administered appropriately and channeled to the correct infusion sites.