An introducer is provided for introducing a sensor into the body of a patient. The introducer connects to a sensor hub. When the sensor hub and introducer are connected, the introducer needle is exposed. When the sensor hub and introducer are disconnected, a needle cover and the needle move with respect to each other so that the needle cover substantially covers the needle, protecting a user from being injured by the needle.

A belt used in an electrocardiographic measurement apparatus includes a belt body to be wrapped around a living body, three or more base electrodes disposed in a longitudinal direction of the belt body, and two or more cap electrodes detachable and attachable to the base electrodes and smaller in number than the number of base electrodes.

A blood pressure monitor configured to removably mount to a cuff in a substantially symmetrical position with respect to a width of the cuff can include a housing defining an interior, a first port, and a second port. The first port can: secure to a first prong of the cuff when the cuff is mounted in a first orientation; receive and secure to a second prong of the cuff when the cuff is mounted in a second orientation; and enable fluid communication between the interior and at least one of a first fluid passage within the first prong and a second fluid passage within the second prong. The second port can: secure to the second prong of the cuff when the cuff is mounted in the first orientation; and receive and secure to the first prong of the cuff when the cuff is mounted in the second orientation.

An apparatus is provided. A strip has first and second end sections, and a first surface and second surface. Two electrocardiographic electrodes are provided on the strip with one of the electrocardiographic electrodes provided on the first surface of the first end section of the strip and another of the electrocardiographic electrodes positioned on the first surface on the second end section of the strip. A flexible circuit is mounted to the second surface of the strip and includes a circuit trace electrically coupled to each of the electrocardiographic electrodes. A wireless transceiver is affixed on one of the first or second end sections, and a battery is positioned on one of the first or second end sections. A processor is positioned on one of the first or second end sections and is housed separate from the battery.

A surgical instrument connectable to a surgical energy module that is configured to provide a first drive signal at a first frequency range for driving a first energy modality and a second drive signal at a second frequency range for driving a second energy modality is provided. The surgical instrument can comprise a surgical instrument component configured to receive power from a direct current (DC) power source, an end effector, and a circuit. The circuit can be configured to convert the first electrical signal to a DC voltage, apply the DC voltage to the surgical instrument component, and deliver the second energy modality to the end effector according to the second drive signal. Alternatively, the circuit can be disposed within a cable assembly configured to connect the surgical instrument to the surgical energy module.

According to certain embodiments, a wearable electronic device comprises: a housing; a first electrode and a second electrode disposed on the housing; an A/D converter connected to the first electrode and the second electrode; a pulse generator connected to the first electrode and the second electrode; and a processor operatively connected to the A/D converter and the pulse generator; wherein the processor is configured to: control the pulse generator to output a series of pulse waves to the first electrode when an external object is in contact with the first electrode; and controlling the A/D converter to obtain biometric information from the first electrode and second electrode in response to outputting the series of pulse waves.

Embodiments of the presently described device, system and method support upper extremity (UE) therapy through tracking the human hand. The system can include a hand-wearable sensor mounting system with hand-wearable components and a movement interpretation circuit. The device can include a hand-wearable component comprising a hook, and a sensing transducer comprising a clip, wherein the clip is detachably securable to the hook. In embodiments, one or more sensing transducers are translationally and rotationally restricted when secured to the hand-wearable components.

Devices associated with on-body analyte sensor units are disclosed. These devices include any of packaging and/or loading systems, applicators and elements of the on-body sensor units themselves. Also, various approaches to connecting electrochemical analyte sensors to and/or within associated on-body analyte sensor units are disclosed. The connector approaches variously involve the use of unique sensor and ancillary element arrangements to facilitate assembly of separate electronics assemblies and sensor elements that are kept apart until the end user brings them together.

The invention relates to a sensor module (10) comprising a first submodule (101) comprising an electronic unit (105) for measuring and transmitting movement data, and a first structure (103), and a second submodule (201) comprising a fastening means for fastening the second submodule (201) to a wearer, and a second structure (205), wherein the first structure (103) can form a reversible mechanical connection with the second structure (205), with the result that the first submodule (101) and the second submodule (201) are reversibly connected to one another.

Apparatus and methods are operative to probe the condition of a sensor either initially, at any point thereafter or continuously during a continuous sensor operation for measuring an analyte in a bodily fluid (such as performed by, e.g., a continuous glucose monitoring (CGM) sensor). Results of the probe may include calibration indices determined from electrical signals obtained during the probe. The calibration indices may indicate whether in-situ adjustment of the sensor's calibration should be performed either initially and/or at random check points. Probing potential modulation parameters also may be used during analyte calculations to reduce the effects of lot-to-lot sensitivity variations, sensitivity drift during monitoring, temperature, interferents, and/or the like. Other aspects are disclosed.