A device may be configured with a housing having a reservoir and an outlet separated by a heat rupturable membrane. The membrane may serve to separate a material held within the reservoir from the outlet until the membrane is ruptured. The membrane may include a heater configured to selectively rupture the membrane when actuated. The heater may be physically removed and/or thermally insulated from at least one of an environment surrounding the device and the reservoir.

A method for improved controlling of a thermic infusion system having a one tubal segment and a thermal element to heat an infusion fluid carried within the tubal segment, and having at least one sensor positioned within the thermic infusion system comprising regulating energy provided to the sensor for a first period of time to sense a self-heating effect of the at least one sensor due to a dry tube; responsive to detecting a dry tube, preventing energizing the thermal element; responsive to detecting a non-dry tube, regulating energy provided to the sensor for a second period of time to sense a temperature of an infusion fluid carried within the at least one tubal segment.

A method for improved controlling of a thermic infusion system having a one tubal segment and a thermal element to heat an infusion fluid carried within the tubal segment, and having at least one sensor positioned within the thermic infusion system comprising regulating energy provided to the sensor for a first period of time to sense a self-heating effect of the at least one sensor due to a dry tube; responsive to detecting a dry tube, preventing energizing the thermal element; responsive to detecting a non-dry tube, regulating energy provided to the sensor for a second period of time to sense a temperature of an infusion fluid carried within the at least one tubal segment.

Provided is a warming device which can efficiently warm a blood product and inhibit a liquid in a warming flow path from exceeding an upper limit temperature thereof when liquid delivery of the blood product is stopped. The warming device includes the warming flow path in which the blood product flows and a heat plate which is in contact with the warming flow path to supply heat to the warming flow path. On the heat plate, a heater in a predetermined pattern corresponding to the warming flow path is disposed. The heater is disposed such that an amount of heat generation toward the warming flow path decreases in stages from an upstream side toward a downstream side in the warming flow path and that a decrease rate of the amount of heat generation at each of the stages decreases from the upstream side toward the downstream side.

Provided is a warming device which can efficiently warm a blood product and inhibit a liquid in a warming flow path from exceeding an upper limit temperature thereof when liquid delivery of the blood product is stopped. The warming device includes the warming flow path in which the blood product flows and a heat plate which is in contact with the warming flow path to supply heat to the warming flow path. On the heat plate, a heater in a predetermined pattern corresponding to the warming flow path is disposed. The heater is disposed such that an amount of heat generation toward the warming flow path decreases in stages from an upstream side toward a downstream side in the warming flow path and that a decrease rate of the amount of heat generation at each of the stages decreases from the upstream side toward the downstream side.

A drug delivery device is provided, the drug delivery device comprising a thermal coupling surface which is arranged and configured to transfer thermal energy, and a thermally controlled member, which is thermally conductively connected to the thermal coupling surface, wherein the thermally controlled member is configured to operate in response to thermal energy transferred through the thermal coupling surface, and wherein the drug delivery device is configured to perform a drug delivery operation.

A drug delivery device is provided, the drug delivery device comprising a thermal coupling surface which is arranged and configured to transfer thermal energy, and a thermally controlled member, which is thermally conductively connected to the thermal coupling surface, wherein the thermally controlled member is configured to operate in response to thermal energy transferred through the thermal coupling surface, and wherein the drug delivery device is configured to perform a drug delivery operation.

An intravenous fluid conditioning system includes a housing having a first chamber and a second chamber. A volume of heat transfer medium is located in the first chamber and the second chamber. A first intravenous fluid line extends through the first chamber and a second intravenous fluid line extends through the second chamber. One or more thermoelectric devices are located in the housing, such that a first side of each of the one or more thermoelectric devices is in thermal communication with the first chamber and a second side of each of the one or more thermoelectric devices opposite the first side is in thermal communication with the second chamber. The one or more thermoelectric devices exchange thermal energy with a volume of intravenous fluid selectably flowed through the first intravenous fluid line or the second intravenous fluid line to condition the intravenous fluid.

A system for mass vaccination includes a plurality of portable electronic injectors, a mobile process manager and a database. Each portable electronic injector includes at least one needle to administer a measured amount of at least one vaccine to a body skin/tissue and an indicator system to provide an indication when either an injection error occurs or when a vaccination indication is required. The mobile process manager is in wireless communication with the plurality of injection devices and controls a mass vaccination. The process manager transmits task data to all injection devices in parallel via WI-FI, receives the vaccination indications from each injector in real time, also receives injection errors and vaccination process data, alerts a vaccination process overseer generally in real-time of the errors and transmits the injection data from each injector via cellular and/or internet transmission to the database.

A system for mass vaccination includes a plurality of portable electronic injectors, a mobile process manager and a database. Each portable electronic injector includes at least one needle to administer a measured amount of at least one vaccine to a body skin/tissue and an indicator system to provide an indication when either an injection error occurs or when a vaccination indication is required. The mobile process manager is in wireless communication with the plurality of injection devices and controls a mass vaccination. The process manager transmits task data to all injection devices in parallel via WI-FI, receives the vaccination indications from each injector in real time, also receives injection errors and vaccination process data, alerts a vaccination process overseer generally in real-time of the errors and transmits the injection data from each injector via cellular and/or internet transmission to the database.