Medical procedure trays and related methods are provided to accommodate joining a first non-sterile medical device with a second sterile medical device and maintaining required sterilization of the second sterile medical device to perform an associated medical procedure. One example of such medical procedures includes biopsy of a bone and/or associated bone marrow using a non-sterile powered driver and a sterile biopsy needle or biopsy needle set. Each medical procedure tray may include a containment bag or sterile sleeve. A coupler assembly, one or more sharps protectors, a biopsy sample ejector and/or associated ejector funnel may also be included. Some medical procedure trays may allow engaging a non-sterile powered driver with one end of a coupler assembly and sealing the non-sterile powered driver in a sterile sleeve or containment bag without compromising sterility of other components in the medical procedure tray.

The present disclosure discloses a disposable cover (4) for covering a head (8) of an optical device (1) and contacting a subject for examination. The cover includes a body (21), defining a first surface (19) and a second surface (20). The body (21) is removably connectable to the head through the first surface and the second surface, where one or more apertures (6) are defined in the first surface (20). A flexible cap (7) is disposed of in each of the one or more apertures of the body, where at least a portion of the flexible cap is made of a substantially transparent material. The flexible cap is structured to accommodate an optical probe (3) extending from the head of the optical device, such that the optical probe extends and retract relative to the body based on position of the optical device relative to the subject.

An oximeter probe includes a probe unit or a base unit and a probe tip where the probe tip has a number of sources and detectors that can be accessed individually or in differing combinations for measuring tissue oxygen saturation at different tissue depth in tissue. A processor of the oximeter probe controls a multiplexer that is coupled to the detectors for selectively collecting measurement information from the detectors via the multiplexer. The oximeter probe is user programmable via one or more input devices on the oximeter probe for selecting the particular sources and detectors to collect measurement information from by the processor.

A method and a device for diagnostic of skin cancer and other mammalian skin tissue pathologies are described. The method relies on determination of pathological changes in tissue vascularization and capillary blood flow. The device uses photonic emitters and detectors to characterize temporal and spatial changes in blood flow in response to external perturbation such as external mechanical force or temperature change.

A medical instrument and method thereof for performing a measurement on a biological sample using a test strip are disclosed. The medical instrument may comprise: an analytical unit for analyzing the test strip, wherein the analytical unit comprises a test strip mount which receives the test strip to perform the measurement; a test strip port which receives the test strip, wherein the test strip port is aligned with the test strip mount along an insertion direction; and a shutter movable between open and closed positions, the shutter comprises a test strip opening, wherein the test strip opening is aligned with the test strip port and the test strip mount when the shutter is in the open position, wherein the shutter comprises a shutter mechanism that rotates the shutter parallel to the insertion direction about a rotational axis to move the shutter between the open position and the closed position.

A sensor cartridge according to embodiments of the disclosure is capable of being used with a non-invasive physiological sensor. Certain embodiments of the sensor cartridge protect the sensor from damage, such as damage due to repeated use, reduce the need for sensor sanitization, or both. Further, embodiments of the sensor cartridge are positionable on the user before insertion in the sensor and allow for improved alignment of the treatment site with the sensor. In addition, the sensor cartridge of certain embodiments of the disclosure can be configured to allow a single sensor to comfortably accommodate treatment sites of various sizes such as for both adult and pediatric applications.

A pressure monitoring system and method for warning a patient or caregiver that soft tissue pressure has exceeded some predetermined level that over time would necessitate moving the patient to prevent or at least reduce a risk of soft tissue damage. The pressure monitoring system and method utilize a dressing assembly adapted to be applied to or near a surface of the patient's body and generate electrical outputs corresponding to soft tissue pressure sensed at the surface. The dressing assembly includes a pocket formed therein for removable, secured and protected insertion of one or more sensors.

Systems and methods are provided for water resistant connectors. A male connector includes a rib or a draft angle that creates a seal when engaged with a female connector. A male connector includes an overmold that includes or is made of a thermoplastic elastomer. Male or female connectors include molds that include or are made of a thermoplastic polymer, such as polypropylene. A female connector includes spring contacts that fit within individual pockets of the female connector.

The present disclosure relates to a sterilization packaging method for a body-attachable biometric monitoring device. Provided is a sterilization packaging method for a body-attachable biometric monitoring device, the method in which a sterilization packaging process can be performed in a convenient and simple manner, further contamination which can occur during a sterilization process is prevented, damages due to moisture and the like after the packaging is complete are also prevented and thus complete sterilization packaging can be performed, in order to separately perform a sterilization packaging step in two steps, primary packaging is performed for a sterilizable state and then sterilization is performed, secondary packaging is performed to maintain airtightness for a primary packaged article which has been sterilized and thus penetration by an external contaminant and the like during the sterilization and packaging processes is prevented to prevent damages to a biometric monitoring device, a separate adsorbent is positioned outside the primary packaged article and then the secondary packaging is performed and thus functional degradation of the adsorbent during the sterilization process is prevented to enable inner packaging of the adsorbent in an excellent functional state, and a moisture removal function can be performed stably to enable a complete sterilization packaging.

A patient monitoring sensor having a communication interface, through which the patient monitoring sensor can communicate with a monitor is provided. The patient monitoring sensor includes a light-emitting diode (LED) communicatively coupled to the communication interface and a detector, communicatively coupled to the communication interface, capable of detecting light. The patient monitoring sensor includes hydrophobic materials provided around the light-emitting diode and the detector, wherein the hydrophobic materials reduce water absorption and prevent bacterial growth within the sensor.