The invention relates to a method and system for providing feedback to a patient using an inhaler of a specific type for inhaling a therapeutic aerosol according to instructions for use provided to the patient with the inhaler. The method comprises the steps of obtaining a sequence of digital audio signals and a sequence of digital video signals emitted from the patient while using the inhaler, recognising the type of the inhaler by processing the video signals, recognising whether the patient has deviated from the instructions by processing the audio and video signals, and recognising the type of the deviation; and presenting to the patient one or more feedback messages indicating whether a deviation was recognised, and if so, what type of deviation occurred, and optionally an inhalation manoeuvre without the deviation.

An apparatus for presenting an application status of a medical device that has a unused state and a used state. The apparatus includes a label having an electrochromic element. The label is at least partially disposed on an exterior surface of the medical device and is configured to display a predetermined feature in response to an electric current. A power source is disposed in or on the medical device for providing the electric current. A switch is configured to selectively connect or disconnect the label and the power source to one another for controlling the application of the electric current to the electrochromic element in response to actuation of the medical device from the unused state to the used state. The label may be scanned by a scan device that may connect to a medical organization for communicating information between the scan device and the medical organization.

A drug tracking device used in combination with a drug injection device. The drug tracking device may comprise a housing configured to engage with the drug injection device, an optical sensor configured to capture an image of a portion of the drug injection device. The portion of the drug injection device displays indicia of drug doses, such that a captured image includes at least one indicia of a drug dose. The drug tracking device may include a memory module having pre-stored indicia of drug doses, and a processor having instructions operating thereon configured to cause the processor to determine an injected drug dose by comparing at least one indicia of the drug dose in the captured image with the pre-stored indicia of drug doses.

A fluid supply warning and communication system including a digital regulator in fluid tight engagement with a primary fluid reservoir. A method of using the fluid supply warning and communication system by flowing a fluid from a primary fluid reservoir to an end use appliance and detecting flow rate and pressure of the fluid with a digital regulator. A gas supply warning and communication system including an oxygen flow monitor that monitors SpO2, flow rate, pulse rate, and battery levels. A method of using the gas supply warning and communication system by flowing oxygen from a primary gas reservoir to an end use appliance, and measuring SpO2, flow rate, pulse rate, tank status, and battery levels.

The present invention relates to an autoinjector device (10) for use in combination with a syringe (30), said syringe comprising a movable plunger; a needle; and a tubular needle shield (34). The claimed autoinjector device (10) comprises: an elongated housing having a proximal(11) and a distal end (12); a drive mechanism; a syringe holder (40) in order to support the fragile syringe and to prevent damage to the syringe. The invention furthermore relates to a method for assembly of the autoinjector device according to the invention.

The present disclosure relates to an autoinjector device for use in combination with a syringe, said syringe comprising a movable plunger; a needle; and a tubular needle shield. The claimed autoinjector device comprises: an elongated housing having a proximal and a distal end; a drive mechanism; a syringe holder in order to support the fragile syringe and to prevent damage to the syringe. The invention furthermore relates to a method for assembly of the autoinjector device according to the invention.

Provided is a microneedle patch which is easily to be applied on a skin surface. One or more holes are provided inside a protective sheet of the microneedle patch, and one or more cutting lines running from an outer edge of the protective sheet toward the holes are also provided. The cutting lines may be symmetrically arranged on both sides of the hole. Providing an incision on the outer edge of the cutting lines of the protective release sheet facilitates cutting along the cutting lines. In the use of the microneedle patch, both sides of the cutting line of the protective release sheet are held and torn so as to bring out a microneedle array adhesive sheet and apply it on a skin. Then the microneedle array surface is slightly compressed, thereby the microneedle is inserted into the stratum corneum.

An apparatus comprising a socket insert that is arranged in a receptacle of the apparatus. The socket insert is connected to an operating medium connector. In the receptacle a data interface is covered by the socket insert and inaccessible from outside. To obtain access to the apparatus software or data, the socket insert can be replaced by a service insert that covers the operating medium output but contacts the data plug. The service insert allows communication with the apparatus control to input or output data and/or programs. The arrangement of the service interface covered by socket inserts provides an effective means for access control to the service interface. It impedes or avoids non-authorized access to the interface and damages for persons and material that otherwise could occur due to the missing disruptive discharge proof potential separation between the service interface and particularly the power section of the apparatus control.

A dialysis system is described having components for facilitating a health-enhanced environment in the vicinity of a dialysis machine in the home. The health-enhancing components may include air improvement components and potable water supply components integrated and/or otherwise incorporated into the home dialysis machine. By incorporating the ability for monitoring, cleaning, and controlling air and/or water quality into the home dialysis machine, the dialysis machine is no longer just a source of life for the dialysis patient but also a source of health enhancement for the entire household. The system may further display and/or remotely communicate information concerning the dialysis treatment, the air quality and the potable water quality corresponding to operation of the dialysis machine in the home environment.

In some embodiments, an adjunct device for tracks time and/or dosage of a medicine. The device may include a connector for mounting the device to a deposable pen injector. The device may be configured to allow use of the native controls and injectors of the injector. For example the device may include a view port for viewing a dose indicator of the injector. The device may include one or more vibration sensors. A processor may be configured to differentiate increasing a dose, decreasing a dose and/or discharging the medicine based on the output of the sensors. Optionally a display of the device may be positioned for simultaneous viewing with the dosage indicator of the injector. For example a user may verify the accuracy of the adjunct device before performing a discharge.