A sterile cover assembly is for a biopsy device. The biopsy device includes a reusable holster including a housing and driving mechanism. The driving mechanism is for driving a cutter in a needle of a probe. The housing is adapted to releasably couple to the probe. The sterile cover assembly includes a sleeve and a flexible sterile cover. The sleeve is configured to receive at least a portion of the housing of the reusable holster. The sterile cover is coupled to the sleeve and is configured to cover the housing of the holster.

A patient monitor configured to receive patient-information electrical signals from an invasive patient sensor and a minimally invasive patient sensor, the patient monitor including a base unit and a detachable user interface unit for displaying hemodynamic parameters determined by the base unit. The base unit and user interface unit can be docked together, tethered together through a cabled connection, or physically separated from one another using wireless communication to transmit and receive information. The base unit and the user interface unit may pair before the user interface unit displays data to link the base unit with the user interface unit. The patient monitor can be configured to switch between invasive and minimally invasive monitoring of hemodynamic parameters of a patient, using invasive measurements to calibrate minimally invasive measurements.

The plaque detecting device of the present invention comprises a light emitting unit (450) which irradiates ultraviolet or blue excitation light (L) toward the tooth surface (99a), and a first and second light receiving units (402) which receive radiated light (L′) from the tooth surface (99a). The first light receiving unit extracts the spectral component of a first wavelength region including the wavelength range of fluorescent light specific to plaque from the radiated light (L′), and obtains a first output value corresponding to the intensity of that spectral component. The second light receiving unit extracts, from the radiated light (L′), the spectral component of a second wavelength region containing the wavelength range of the fluorescent light specific to enamel and having a predetermined lower limit wavelength below the lower limit wavelength of the first wavelength region, and obtains a second output value corresponding to the intensity of this spectral component. Determination of the relative magnitude of the ratio between the first output value and the second output value as compared to a first threshold value is performed. Determination of the relative magnitude of the difference between the first output value and the second output value as compared to a second threshold value is performed.

Methods and devices and systems include generating analyte data based on signals from an analyte sensor transcutaneously positioned in contact with interstitial fluid under a skin layer of a user and to generate signals corresponding to an analyte level of a target analyte. The analyte data corresponds to the analyte level of the target analyte over a wear period. Methods include storing the analyte data over the wear period. Methods include determining one or more indications based on the analyte data. Methods include determining a reimbursement insurance code based at least in part on stored sensor information associated with the analyte sensor. Methods include communicating at least a portion of the analyte data and the reimbursement insurance code to an electronic record associated with the user and stored by a remote electronic medical record system. Methods include providing the one or more indications on a user interface unit.

An energy module is disclosed. The energy module includes a control circuit and a two wire interface coupled to the control circuit. The two wire interface is configured as a power source and as a communication interface between the energy module and a neutral electrode.

Disclosed is a system (100) for inserting an adapter. The system can include a docking station (104) and an adapter inserter (102). The docking station can include a handle block (108), a push assembly, and a linkage (320) connecting knob push handle (120) to an engagement tube pull block (324). The engagement tube pull block (324) can extend from the linkage through a portion of the handle bock. The adapter inserter (102) can include a handle body (112), an engagement assembly (116), and a clamp (412). The handle body can be sized to fit in a first recess (110) defined by the handle block body. The engagement assembly (116) can extend from a second end of the handle body (112) and can be configured to engage the adapter (132) at a tip of the engagement assembly. The clamp (412) can be located within and proximate a second end of the handle body so as to engage a portion of the engagement assembly.

In an embodiment, a method includes receiving, by a user device, a code start trigger, where the user device is dockable on a crash cart and in communication with a controller disposed in relation to the crash cart. The method also includes, responsive to the code start trigger, initiating a code workflow, creating an event log for the code workflow, and determining a patient rhythm. The method also includes monitoring for real-time code events. The monitored real-time code events include patient intervention and a new patient rhythm. The method also includes, responsive to a determination that a real-time code event has occurred, executing programmed action that includes updating the event log.

A system and method for comprehensive remote monitoring of a user's vital signs and bodily functions includes a wearable monitor in bi-directional communication with a gateway element that communicates with one or more external devices to allow remote access to user vital sign and bodily function information.

A system and method for collecting operation data associated with a medical apparatus including an internal device implanted in a subject and an external device that is magnetically-coupled to and drives the internal device. The medical apparatus may be monitored to obtain raw data associated with the operation of the medical apparatus and one or more calculations may be performed on the raw data, wherein the raw data and/or calculated values may be associated with voiding frequency and voiding volume of the subject. A report may be generated from the raw data and/or calculated values. In addition, one or more signals may be sent to the external device and/or a docking station, or communicated by other means, to indicate to the subject that the operation of the medical apparatus should be altered.

A surgical robotic system comprising: a robotic arm; a tool drive coupled to the robotic arm; a cannula interface configured to couple a cannula to the tool drive, the cannula interface having a fluid pathway in communication with an interior lumen of the cannula; and an insufflation pathway coupled to the robotic arm, the insufflation pathway having a distal end coupled to the fluid pathway and a proximal end coupled to a surgical insufflator.