The present disclosure relates to a method for identifying a user interface. Flow data associated with air flowing in a respiratory therapy system is received. Acoustic data associated with the respiratory therapy system is received. The received flow data and the received acoustic data are analyzed. Based at least in part on the analysis, a mask type for the user interface is determined.

Adherence monitors are disclosed, incorporating cap removal sensors together with a determined time period in order to determine that a dose of medicament has been dispensed. In another form, cap removal data is combined with acoustic data to determine that a dose of medicament has been dispensed. Several specific structural arrangements are also disclosed.

A medication injection device includes a barrel and a plunger disposed to dispense a fluid from the barrel. A dosage tracking system is coupled to output data indicative of the fluid dispensed. A controller is disposed within the medication injection device and coupled to receive the data from the dosage tracking system. The controller includes logic that when executed by the controller causes the controller to perform operations including determining, based on the data, whether an air shot event occurred while dispensing the fluid.

A monitoring device for monitoring operation of a drug delivery device and to a respective drug delivery device is presented in which a fastening member releasably attaches the monitoring device to an axially elongated housing of the drug delivery device, a sliding member is shiftable relative to the fastening member in an axial direction and being adapted to operably engage with at least one dose setting component of the drug delivery device to follow an axial displacement of the dose setting component relative to the housing component, a first sensor arrangement for detecting a rotation of the dose setting component relative to the fastening member, a second sensor arrangement for detecting an axial displacement of the sliding member relative to the fastening member, and a processing member coupled to the first and to the second sensor arrangements to process first and second signals obtainable from the first and from the second sensor arrangements for determining the size of a dose dispensed by the drug delivery device.

The pharmaceutical injection device includes a pharmaceutical syringe mounting portion (3) provided within a main body case (2) and to which a pharmaceutical syringe (4) is removably mounted, a piston (5) provided movably with respect to the pharmaceutical syringe (4) mounted to the pharmaceutical syringe mounting portion (3), a drive mechanism (6) for driving the piston (5), a controller (7) that is electrically connected to the drive mechanism (6), a display section (35) that is connected to the controller (7), and an encoder (26) that is connected to the controller (7) and detects the amount of the pharmaceutical remaining inside the pharmaceutical syringe (4). The controller (7) displays a warning on the display section (35) recommending removal of the pharmaceutical syringe (4) from the pharmaceutical syringe mounting portion (3) when the presence of a pharmaceutical is detected by the encoder (26).

Various embodiments of a “smart” drug delivery pen are provided which include a drug delivery pen having an inertial sensor or accelerometer. A system is also provided that includes the smart drug pen in conjunction with a data management unit(s) DMU. Various exemplary methods for use of the pens and systems are also described and illustrated.

A medicament delivery device is presented having a housing configured to accommodate a medicament container filled with medicament, a drive unit comprising a plunger rod operable to act on the medicament container, a mechanical activation mechanism configured to interact with the drive unit, where the mechanical activation mechanism is movable between certain predetermined states when interacting with the drive unit, a recording unit capable of recording status changes of the medicament delivery device including the status of the mechanical activation mechanism, and detection elements operably connected to the recording unit and positioned such as to detect when the activation mechanism has been moved between certain predetermined states.

Provided is an aerosol generating system including a holder configured to generate aerosol by heating a cigarette; and a cradle including an inner space into which the holder is inserted. The holder is configured to be tiltable with respect the cradle. The holder is inserted into the inner space of the cradle and then tilted to generate the aerosol.

A system and method are disclosed in the field of preparing a catheter for use in a patient, in particular a catheter of an intravascular blood pump, more specifically for properly purging and de-airing the catheter. The catheter comprises an elongate tubular portion and a connected device. The elongate tubular portion is configured to be inserted into a patient's blood vessel and defines a lumen. The connected device is connected to the elongate tubular portion and has a cavity, which may accommodate a drive unit of the blood pump, and which is in fluid communication with the lumen of the elongate tubular portion. In order to securely de-air the system, a sensor, such as an accelerometer, for detecting an orientation of the connected device is provided, and a user may be guided to correct the orientation of the connected device for proper purging.

This invention refers to a device that reduces and counteracts human motor symptoms (tremor in the upper limbs, muscular stiffness, bradykinesia or slowness in movements, postural disruptions, Parkinsonian walking and freezing in the walking) caused by Parkinson's disease. The device produces vibration by means of a micro-motor that can be modulated in time, speed and power. A laser diode generates a light that is projected in the ground in the form of a horizontal line, a Bluetooth module communicates this device with different intelligent electronic devices and with applications. These components are powered by a rechargeable handheld power source. The components are powered by a rechargeable handheld electric energy source.