Various exemplary drug holders (102, 200) for drug delivery devices (100), drug products utilizing the same, and methods of using drug holders for drug delivery devices are provided. In general, a nasal drug delivery device is configured to dispense therefrom at least one dose of a drug therefrom into a nose. The drug delivery device includes a drug holder that contains the drug therein that is delivered out of the drug delivery device. The drug holder can include two cavities (208, 210) therein that are fluidically sealed from one another prior to use of the drug delivery device to cause drug delivery. A first one of the cavities includes the drug therein, and a second one of the cavities includes a drug or air therein.

An infusion needle structure of drug infusion device includes: an infusion needle including a front end and a back end; a needle holder provided with at least one auxiliary fastener; one fastening portion, arranged inside the infusion device, cooperates with the auxiliary fastener to lock the needle holder in the working position; an unlock hole provided on the needle holder or on the housing of the infusion device; and an unlock rod that is inserted into the unlock hole and pushed, thus releasing and resetting the needle holder. The infusion needle is able to reset and released when the infusion device is during replacement.

Methods and apparatus for acquiring data associated with a monitored analyte level, determining a glucose level based at least in part on the acquired data associated with the monitored analyte level, manipulating a data set based on a processing mode following the glucose level determination, where the processing mode includes one of a data set transmission and output display, a data set storing and output display without transmission, or a data set transmission and data set storing without output display are provided.

A medication delivery device having a lock element. The device is connectable to an electrical plug of a conduit. The device includes an external housing with an opening that ports to a plug receiving hollow within an interior volume. An electrical circuit connected to at least one of a rechargeable battery and a memory controller includes a connection element within the plug receiving hollow. The lock element travels within the plug receiving hollow when a dose delivery assembly of the device operates for forcing medication from the device. The lock element is sized and positioned to have its travel halted by abutment with the plug, when the plug is within the plug receiving hollow and electrically interfacing with the connection element, to thereby halt the dose delivery assembly from further operating for forcing medication from the device.

The present invention relates to a system for obtaining medicament related information of specific medicaments, the in system comprising a device (10, 50) for obtaining medicament related information, the device comprising a recording unit, said recording unit comprising a reader (20, 32; 86, 88, 92, 122), capable of reading information pertained to specific medicaments, said recording unit further comprising a memory module (22, 104) capable of storing information read by said reader (20, 32; 86, 88, 92, 122), wherein said reader (20, 32; 86, 88, 92, 122) is arranged with a three-dimensional contact interface (81) designed to interact with a corresponding contact surface (87) containing information related to specific medicaments.

Techniques disclosed herein relate to operating a fluid delivery device in a personalized manner based at least in part on historical data of a patient. In some embodiments, the techniques involve determining a predicted physiological condition of a patient in response to a future activity of the patient, based at least in part on historical data corresponding to the future activity for the patient; determining, based at least in part on the predicted physiological condition of the patient, an adjustment to fluid delivery to the patient by a medical device to prospectively account for the future activity; and operating the medical device to deliver a fluid to the patient in accordance with the adjustment.

A tubeset module includes one or more elements of a negative pressure wound therapy (“NPWT”) system, such as a valve, a calibrated leak, a pressure sensor, etc. The tubeset module may communicate with a controller of the NPWT system via a communications interface provided by the tubeset module. The communication between the tubeset module and the controller may be used to fully automate one or more processes involving the operation of the components of the NPWT system included in the tubeset module, allowing the NPWT system to, e.g. estimate a wound site volume, estimate a volume of fluid to be instilled, monitor wound healing progression, etc. without requiring any user interaction or involvement. The tubeset module may be defined by one or more housing elements. The tubeset module may be incorporated into any of the tubing, fluid canister, wound dressing and/or therapy device housing components of the NPWT system.

A system for generating a hypoglycemia risk signal associated with exercise-induced Hypoglycemia. The system can include a processor configured to obtain a blood glucose signal (BG.sub.start), a ratio of absolute insulin on board over total daily insulin signal (IOB.sub.abs/TDI), and an initial glycemic slope signal (S.sub.0); generate a hypoglycemia risk signal based on a hypoglycemia prediction algorithm that determines the probability of a user being hypoglycemic during or after exercise based on the obtained BG.sub.start, IOB.sub.abs/TDI and S.sub.0.

Infusion systems, infusion devices, and related operating methods are provided. An exemplary method of operating an infusion device capable of delivering fluid to a patient involves obtaining, by a control system associated with the infusion device, measurement values indicative of a condition of the patient provided by a sensing device, identifying an event pattern based at least in part on the measurement values for the condition and historical data associated with the patient, generating a notification indicative of the event pattern in response to identifying the event pattern, and adjusting operation of the infusion device to deliver the fluid to the patient in a manner that is influenced by the event pattern in response to receiving user input confirming the event pattern.

This medical container includes a barrel defining a reservoir for containing a medical product, and a needle extending in a barrel channel provided at a distal end of the barrel so as to establish a fluid communication between the reservoir and the needle. The medical container further includes a RFID on-metal (ROM) tag, said RFID on-metal tag being located at least partly inside the barrel channel and having an antenna extending along the needle.