Systems and methods for securely transferring medical data for an off-site administered test. A method includes receiving, at a first device, a key associated with a second device from a third device, wherein the second device is a medical device having a unique identifier, wherein the second device includes at least one sensor configured to capture medical data; receiving, at the first device, a request to store the medical data captured by the at least one sensor from the second device; configuring the second device to store the medical data in at least one designated storage location, wherein each designated storage location is accessible to the second device and to the third device; and sending the designated storage location and the unique identifier to the third device.

Generally, methods, devices, and systems related to analyte monitoring and data logging are provided—e.g., as related to in vivo analyte monitoring devices and systems. In some aspects, methods, devices, and systems are provided that relate to enable related settings based on an expected use of an in vivo positioned sensor; logging or otherwise recording analyte levels acquired or derived—e.g., sample analyte levels more frequently than they are logged or otherwise recorded in memory; dynamically adjust the data logging frequency; randomly determine times of acquiring or storing analyte levels from the in-vivo positioned analyte sensors; and enable recording related settings when the system is operable.

A surgical instrument is disclosed. The surgical instrument includes a shaft, a sensing array and a fluid detection circuit. The sensing array is positioned within the shaft. The fluid detection circuit is electrically coupled to the sensing array, and is configured to determine when a fluid originating from an environment external to the shaft is present within the shaft.

A method for labelling a portion of a device includes the steps of providing a first substrate layer of a transparent or translucent material, depositing a first coloured material onto the first substrate layer in a labelling portion of the layer, thereby obtaining a labelling item, and coupling the labelling item to the device. The method is particularly suitable for producing labelled stretchable devices such as soft body-implantable devices for sensing a physiological signal and/or stimulating an electrical and/or pharmacological activity of a body tissue or organ in a subject.

The present invention protects a system for monitoring the vital signs of a user of a disposable absorbent article that comprises a sensor device, a bi-dimensional code and a receiver, such that the sensor device is placed in contact with the user and the system is triggered by the reading of the bi-dimensional code through the receiver, such that the bi-dimensional code is place inside the packaging of the disposable absorbent article.

A sensing system and a pairing method thereof are provided. The pairing method of the sensing system includes: respectively disposing a plurality of sensors on a plurality of parts of a tested subject; setting the tested subjected to perform at least one setting posture, and setting the sensors to respectively provide a plurality of direction information; receiving the direction information respectively provided by the sensors; and identifying the parts where the sensors are respectively arranged according to the direction information. Wherein, when the tested subject performs any one of the at least one setting posture, at least two of the direction information provided by the sensors are different.

A medical device includes a printed circuit board-battery assembly, a tape encapsulation assembly wrapped around the PCB-battery assembly, and a second removable tab positioned on a surface of the tape encapsulation assembly. The second removable tab provides an adhesive layer on a surface of the medical device when the second removable tab is removed from the medical device. The PCB includes the electronic circuitry that performs the functionalities of the medical device, including an optical sensor that comprises at least one light source to emit light towards a measurement site of a user and at least one photodetector to receive light returned from the measurement site. The medical device can connect to a host computing device that performs various operations, including, but not limited to, authenticating the medical device, causing measurement values such as blood oxygen saturation (SpO2), pulse rate (PR), and a perfusion index (PI) to be provided.

A spinal implant assembly includes a set screw having a central opening that extends from a first end of the set screw toward a second end of the set screw. The second end of the set screw includes a bottom bore portion, and the set screw is configured to engage with an anchoring member. The spinal implant assembly includes a capacitive assembly having an integrated circuit located within an internal portion the capacitive assembly, and a plurality of capacitive plates positioned on an outside bottom surface of the capacitive assembly. Each of the capacitive plates is in operable communication with the integrated circuit, and the capacitive assembly is configured to be received within the central opening of the set screw, such that the plurality of capacitive plates are positioned above the bottom bore portion.

A first medical device can receive a physiological parameter value from a second medical device. The second physiological parameter value may be formatted according to a protocol not used by the first medical device such that the first medical device is not able to process the second physiological parameter value to produce a displayable output value. The first medical device can pass the physiological parameter data from the first medical device to a separate translation module and receive translated parameter data from the translation module at the first medical device. The translated parameter data can be processed for display by the first medical device. The first medical device can output a value from the translated parameter data for display on the first medical device or an auxiliary device.

A system that includes at least one processor and a non-transitory, tangible memory device having programming instructions. When the instructions are executed by the at least one processor, the at least one processor receives from a set of sensors at least one biological parameter of an animal in a walk-in analysis zone to create real-time biological. The at least one processor analyzes the real-time biological data from the walk-in analysis zone and recommends animal feed nutrients based on the analyzed real-time biological data. The at least one processor communicates the recommended animal feed nutrients to at least one of: a mobile communication device; and a display device in proximity to the walk-in analysis zone.