A highly integrated analyte detection device, includes: a bottom case; a sensor including a signal output portion and a detection portion; a transmitter provided with at least two second electrical connection ends which are corresponding to the first electrical connection ends; and a connection member, arranged between the first electrical connection ends and the second electrical connection ends, including at least two conductive areas and at least one insulation area. The insulation area is provided between two adjacent conductive areas, and at least two first electrical connection ends are respectively electrically connected to the corresponding second electrical connection ends.

An example wearable electronic device includes a housing including a rear cover having a first hole and at least partially contacting a body of a user while the wearable electronic device is worn by the user, a first biometric sensor disposed in the housing and aligned with the first hole, wherein the first biometric sensor includes a first lens disposed in the first hole and is configured to detect first biometric information of the user based on light of a designated wavelength band, which passes through the first lens, a second biometric sensor disposed in the housing and disposed to face the rear cover, wherein the second biometric sensor is configured to detect second biometric information that is different from the first biometric information, and a blocking structure that prevents or reduces foreign substances from being introduced through the first hole.

A sensor (e.g., an optical sensor) that may be implanted within a living animal (e.g., a human) and may be used to measure an analyte (e.g., glucose or oxygen) in a medium (e.g., interstitial fluid, blood, or intraperitoneal fluid) within the animal. The sensor may include a sensor housing, an analyte indicator covering at least a portion of the sensor housing, and one or more compounds containing boronate or boronic acid moieties that reduce degradation of the analyte indicator.

Systems may include a watch band, a watch body including at least one image sensor configured to capture a wide-angle image, a coupling mechanism configured to detachably couple the watch body to the watch band, and at least one biometric sensor on at least one of the watch band or the watch body. Various other related methods and systems.

A system includes a sensor applicator, a sensor control device arranged within the sensor applicator and including an electronics housing and a sensor extending from a bottom of the electronics housing, and a cap coupled to one of the sensor applicator and the sensor control device, wherein the cap is removable prior to deploying the sensor control device from the sensor applicator.

A medical patch configured for being applied to a patient and for communicating with an in-vivo device located within the patient’s body; The medical patch comprises an adhesive surface configured for adhering the patch to the patient’s skin; and a communication arrangement configured for providing communication between the medical patch and the in-vivo device.

A physiological signal monitoring device includes a base, a biosensor and a transmitter. The biosensor includes a sensing section. The transmitter includes a connection part. The connection part and the signal output section cooperatively form a connection portion after the transmitter moving from an initial position to an assembled position. A safety gap is formed between the transmitter and the biosensor. When the transmitter moves from the initial position toward the assembled position, the safety gap serves to prevent at least one of the connection part of the transmitter and the signal output section of the biosensor from collision.

Embodiments of the invention provide compositions useful in implantable devices such as analyte sensors as well as methods for making and using such compositions and devices. In typical embodiments of the invention, the device is a glucose sensor comprising a polymeric composition disposed on a flexible assembly within the sensor that includes amounts of one or more immunosuppressant agents designed to provide such sensors with improved material properties such as enhanced biocompatibility.

A pressure compensating non-invasive blood-component measuring device has electrically insulated parallel electrodes mounted on a dielectric membrane (106). A main circuit board (201) provides electrical connections to the electrodes and has an orifice (402) to allow flexing. A housing supports the main circuit board, with a second orifice to facilitate the application of a finger onto the insulated electrodes. A bottom circuit board (401) supports a force sensor (408) and fixing elements (313, 314) secure the bottom circuit board to the top circuit board, such that the bottom circuit board does not contact the housing directly. An intermediate board (316) is guided but not restrained by the fixing elements, and is arranged to apply force onto said force sensor.

A biosensor assembly that measures multiple physical parameters is disclosed. The biosensor assembly includes a first implantable probe and a first skin contacting electrode. Wherein a first physiological parameter is measured between the first implantable probe and the first skin contactable electrode.