Surgical instrument with articulation region

A surgical instrument (10, 110, 210) includes an articulating tube assembly (20, 120, 220) having a proximal end and a distal end, an articulating region (23, 123, 223) disposed between the proximal end and the distal end, and a proximal axis axially extending from the proximal end to the articulating region (23, 123, 223). The articulating tube assembly (20, 120, 220) includes an inner tube (24, 124, 224) and an outer tube (26, 126, 226) each having the articulating region (23, 123, 223). The inner tube (24, 124, 224) and the outer tube (26, 126, 226) being movable relative to each other proximal to the articulating region (23, 123, 223) and fixed axially relative one another distal to the articulating region (23, 123, 223). The surgical instrument (10, 110, 210) also includes an actuation assembly (22, 122, 222a) coupled to the articulating tube assembly (20, 120, 220) for moving the inner tube (24, 124, 224) and the outer tube (26, 126, 226) axially relative to each other for articulating the articulating region (23, 123, 223) of the articulating tube assembly (20, 120, 220) between a first configuration and a second configuration, wherein the articulating region (23, 123, 223) is rigid in the first configuration and the second configuration.

SYSTEM FOR DISPLAYING MEDICAL MONITORING DATA

A patient monitoring hub can communicate bidirectionally with external devices such as a board-in-cable or a dongle. Medical data can be communicated from the patient monitoring hub to the external devices to cause the external devices to initiate actions. For example, an external device can perform calculations based on data received from the patient monitoring hub, or take other actions (for example, creating a new patient profile, resetting baseline values for algorithms, calibrating algorithms, etc.). The external device can also communicate display characteristics associated with its data to the monitoring hub. The monitoring hub can calculate a set of options for combined layouts corresponding to different external devices or parameters. A display option may be selected for arranging a display screen estate on the monitoring hub.

Managing dynamic licenses for physiological parameters in a patient monitoring environment

A dynamic licensing system permits facility administrators to quickly enable a patient monitoring device to monitor a previously unmonitored physiological parameter when the caregiver determines that a new physiological parameter should be monitored. The administrator selects through a dynamic licensing module the patient monitoring device and instructs the dynamic licensing system to enable monitoring of the new physiological parameter. The administrator defines how long the patient monitoring device is to be monitoring the new parameter. The administrator may also select locations in the hospital, and some or all patient monitoring devices at that location are upgraded to monitor the new parameter. The dynamic licensing system creates a licensing agreement to monitor the new parameter for the monitoring duration and/or in the monitoring location.

REUSABLE POWERED SURGICAL DEVICES HAVING IMPROVED DURABILITY

A surgical device includes at least one electronic component having a moisture collection agent sealed therein that is configured to protect electronic elements of the electronic component and/or a moisture mitigation system including a moisture migration component disposed within the surgical device and a moisture collection agent disposed adjacent to the moisture migration component to remove moisture from within the surgical device. The at least one electronic component may include a substrate, electronic elements disposed on a surface of the substrate, a coating covering the surface of the substrate and the electronic elements disposed thereon, and a moisture collection agent disposed between the substrate and the coating to control moisture at the surface of the substrate. The at least one electronic component may include a substrate having a base and a cover defining a sealed cavity therein, and electronic elements and a moisture collection agent disposed within the sealed cavity.

System for displaying medical monitoring data

A patient monitoring hub can communicate bidirectionally with external devices such as a board-in-cable or a dongle. Medical data can be communicated from the patient monitoring hub to the external devices to cause the external devices to initiate actions. For example, an external device can perform calculations based on data received from the patient monitoring hub, or take other actions (for example, creating a new patient profile, resetting baseline values for algorithms, calibrating algorithms, etc.). The external device can also communicate display characteristics associated with its data to the monitoring hub. The monitoring hub can calculate a set of options for combined layouts corresponding to different external devices or parameters. A display option may be selected for arranging a display screen estate on the monitoring hub.

Modular multi-parameter patient monitoring device

A multi-parameter patient monitoring device rack can dock a plurality of patient monitor modules and can communicate with a separate display unit. A signal processing unit can be incorporated into the device rack. A graphics processing unit can be attached to the display unit. The device rack and the graphic display unit can have improved heat dissipation and drip-proof features. The multi-parameter patient monitoring device rack can provide interchangeability and versatility to a multi-parameter patient monitoring system by allowing use of different display units and monitoring of different combinations of parameters. A dual-use patient monitor module can have its own display unit configured for displaying one or more parameters when used as a stand-alone device, and can be docked into the device rack when a handle on the module is folded down.

Methods for depositing a conformal metal or metalloid silicon nitride film and resultant films

Described herein are conformal films and methods for forming a conformal Group 4, 5, 6, 13 metal or metalloid doped silicon nitride dielectric film. In one aspect, there is provided a method of forming an aluminum silicon nitride film comprising the steps of: providing a substrate in a reactor; introducing into the reactor an at least one metal precursor which reacts on at least a portion of the surface of the substrate to provide a chemisorbed layer; purging the reactor with a purge gas; introducing into the reactor an organoaminosilane precursors to react on at least a portion of the surface of the substrate to provide a chemisorbed layer; introducing a plasma comprising nitrogen and an inert gas into the reactor to react with at least a portion of the chemisorbed layer and provide at least one reactive site wherein the plasma is generated at a power density ranging from about 0.01 to about 1.5 W/cm2; and optionally purge the reactor with an inert gas; and wherein the steps are repeated until a desired thickness of the aluminum nitride film is obtained.

SYSTEM AND METHOD FOR MANAGING THE USE OF SURGICAL INSTRUMENTS

Disclosed herein are systems and methods for managing surgical instruments. The method includes storing expected processing times associated with managing a group of surgical instrument trays being processed through a sterilization processing department, the expected processing times comprising at least a first expected processing time associated with the first portion of processing the group of surgical instrument trays through the department and a second expected processing time associated with the second portion of processing the group of surgical instrument trays, tracking, in real-time, the group of surgical instrument trays through the sterilization processing department and comparing the time-based data to the expected processing times to identify a discrepancy associated with a respective surgical instrument tray of the group of surgical instrument trays. The method includes identifying metadata associated with the respective surgical instrument tray and transmitting an alert to a device based on the discrepancy and the metadata.

ANTI-DENGUE VIRUS ANTIBODIES AND USES THEREOF

The present invention provides, among other things, antibody agents (e.g., antibodies, and/or antigen-binding fragments thereof) that bind to DV epitopes, as well as compositions containing them and methods of designing, providing, formulating, using, identifying and/or characterizing them. In some embodiments, provided antibody agents show significant binding to a plurality of DV serotypes. In some embodiments, provided antibody agents show significant binding to all four DV serotypes. Such antibody agents are useful, for example, in the prophylaxis, treatment, diagnosis, and/or study of DV.

Surgical robotic assemblies and instrument adapters thereof

An instrument adapter includes a housing, a drive member, a nut, and a shaft assembly. The nut is threadedly coupled to the drive member and axially movable relative thereto. The shaft assembly includes a shaft and a link. The shaft extends distally from the housing and is configured to be operably coupled to an end effector. The link has a proximal end movably coupled to the nut and a distal end configured to selectively lock the end effector to the shaft assembly. The link is movable between a proximal non-locking position, and a distal locking position. The nut is movable between a first position along the drive member, in which the nut resists proximal movement of the link from the distal position to the proximal position, and a second position, in which the nut does not resist proximal movement of the link from the distal position to the proximal position.