A removable wearable device sleeve includes a sleeve body, one or more sensors, and an interface for operative communication with the wearable device. A removable sleeve includes a sleeve body having a front element having a first aperture, a back element having a second aperture, a tubular element having a first end and a second end with a third aperture, and one or more back elements define a cavity to encase an earpiece, an interface, and a sensor, wherein the sensor communicates sensor readings to the wearable device through the interface. A method of placing a sensor configured to communicate with a wearable device onto the wearable device includes providing a removable sleeve and inserting the wearable device through the first aperture of the front element into the cavity of the removable sleeve to provide a removable wearable device sleeve.

The present invention discloses a holder carrying thereon a sensor to measure a physiological signal of an analyte in a biological fluid, wherein the sensor has a signal detection end and a signal output end, and the holder includes an implantation hole being a channel for implanting the sensor and containing a part of the sensor, a fixing indentation containing the sensor, a filler disposed in the fixing indentation to retain the sensor in the holder, and a blocking element disposed between the implantation hole and the fixing indentation to hold the sensor in the holder and restrict the filler in the fixing indentation.

An analyte detection device with intelligent identification function, includes: a transmitter; a sensor unit including a sensor base and a sensor with first parameter, and one end of the sensor inserted under the skin while the other end is installed in/on the sensor base; a bottom base; at least one physical unit with second parameter which corresponds to the first parameter arranged on the bottom base, on the sensor base or on/in the transmitter; and a detection circuit for detecting the second parameter which can be transmitted to the transmitter. Using this detection device, the transmitter can automatically identify the corresponding sensor information.

A biosensing device includes a sensor module and an electric signal transducer. The sensor module includes a biosensor adapted for measuring a biosignal of a host, and a fixed seat including a conducting member that is electrically connected to the biosensor. The electric signal transducer is for receiving and sending the biosignal measured by the biosensor, is coupled to the sensor module, and includes an electric signal unit electrically connected to the conducting member, and a battery connected to the electric signal unit. The electric signal unit has two electrical contacts that cooperatively define a switch. The battery provides power supply to the biosensor when the electric signal transducer is coupled to the sensor module.

A probe includes an insertion portion insertable into a body organ, a projecting portion being exposed to an outside of a body after the insertion portion is inserted into the body organ, a device mounting area onto which an external-device coupler is removably mountable, and sensing electrodes provided on the insertion portion and the device mounting area. When the insertion portion is inserted into the body organ, the sensing electrodes detect a biosignal and become conductive with coupling electrodes of the external-device coupler mounted onto the device mounting area. The probe is an electromyograph probe that detects a biosignal measurable by an electromyograph. The insertion portion and the projecting portion of the probe may be integrated or separate from each other. Both of the insertion portion and the projecting portion or only the insertion portion may be disposable.

Long-term electrocardiographic and physiological monitoring over a period lasting up to several years in duration can be provided through a continuously-recording insertable cardiac monitor. The sensing circuitry and the physical layout of the electrodes are specifically optimized to capture electrical signals from the propagation of low amplitude, relatively low frequency content cardiac action potentials, particularly the P-waves that are generated during atrial activation and storing samples of captured signals. In general, the ICM is intended to be implanted centrally and positioned axially and either over the sternum or slightly to either the left or right of the sternal midline in the parasternal region of the chest.

A second device comprises at least one ADC. The ADC(s) are configured to receive a composite analog signal. The composite analog signal comprises a plurality of modulated signals. Each signal in the modulated signals has been modulated to a distinct center frequency. Each signal in the modulated signals has originated from a sensor. At least two of the signals in the modulated signals comprise a plurality of frequency components. The ADC(s) are configured to convert the modulated signals into a digital signal. The second device comprises at least one control unit. The control unit(s) are configured to receive the digital signal. The control unit(s) are configured to perform: band pass filtering, frequency demodulation, and extraction of the signals sensed by the sensors.

A hand-held vision sensor apparatus comprises a plurality of light sources, control activation elements and an image sensing array, encased within a housing such that the control activation elements are disposed at a user-accessible location on the housing. The housing further includes a pair of exit apertures for emitting illumination directed toward a medical specimen and an entrance aperture for capturing reflected light from the medical specimen. The light sources are disposed in alignment with the pair of exit apertures, and the image sensing array is aligned with the entrance aperture. The control activation elements are utilized to energize the light sources and control the functioning of the image sensing array. A computer port may be included and used to communicate command controls to the light sources, image sensing array and control activation elements in a manner that allows for a remotely-located technician to communicate with the hand-held vision sensor.

An optical probe comprises three optical elements including at least one light source and at least one light detector. The three optical elements are positioned in a triangular configuration. Three optical fibers are each coupled to one of the three optical elements and have an exposed distal end portion. At least one light shroud is disposed radially around the exposed distal end portions of at least one of the optical fibers coupled to the at least one light source.

A system for remote transdermal alcohol monitoring includes and/or interfaces with a transdermal alcohol sensing device. Additionally or alternatively, the system can include and/or interface with any or all of: a user device; a supplementary alcohol sensing device; a set of supplementary sensors; a computing subsystem; a user interface; and/or any other components. A method for remote transdermal alcohol monitoring includes: receiving a set of inputs; determining a set of outputs; and triggering an action based on the set of outputs.