In some embodiments, a kit for preparing a cell suspension may include a device and a housing. The device may include a first label identifying a first reservoir of the device for use with a first portion of a tissue processing method and a second label identifying a second reservoir of the device for use with a second portion of the tissue processing method. The housing includes a first housing portion configured to store a first set of components associated with the first portion of the tissue processing method. The first housing portion includes a first visual indicator associated with the first label of the device. The second housing portion may be configured to store a second set of components associated with the second portion of the tissue processing method. The second housing portion may include a second visual indicator associated with the second label of the device.

Adaptable medical trays are disclosed herein. An adaptable medical tray includes a first component medical tray having a plurality of walls, a bottom, and a removable top, the plurality of walls and the bottom arranged to form a cavity in the first component medical tray; and a second component medical tray removably coupled to the first component medical tray, the second component medical tray including a plurality of walls, a bottom, and a removable top, the plurality of walls and the bottom arranged to form a cavity in the second component medical tray. The first component medical tray and the second component medical tray are constructed of a sterilizable material and the first component medical tray is decouplable from the second component medical tray after a sterilization process without removing the removable tops from the cavities.

A system for packaging a kit for a radiofrequency ablation procedure protects a radiofrequency ablation kit without compromising its sterile barrier system through the hazards of handling, distribution, and storage. The system includes: an introducer tray configured to hold at least one introducer; a probe tray configured to hold at least one radiofrequency ablation probe; an outer carrier tray, a pouch configured to hold a tubing kit; and a dispenser carton. The introducer tray and the probe tray are held within the outer carrier tray, and the outer carrier tray and the pouch are configured to be held within the dispenser carton. A method of packaging a radiofrequency ablation kit is further described.

Systems and methods for remote communications are described. In some embodiments, a telecommunications system may include a case that houses a plurality of antennas, one or more access credentials, and a computing device comprising a processor. The system may be configured to: generate or obtain a plurality of data packets for transmission to a remote site, establish communications links with a plurality of communication nodes, transmit data packets to the first node and the second node, detect an interruption in a communication link to the first node, and transmit a third set of data packets to the second node that would have been sent to the first node in the absence of the detected interruption.

A storage tray provides storage for multiple types of wires, catheters, and other instruments used during surgical procedures. The storage tray includes a base and a set of walls forming a basin that holds liquid. A wire containment section within the basin holds multiple coiled guidewires in a channel filled with the liquid. The wire containment section includes an inner wall and one or more wall segments forming an outer boundary of the channel. A wire holder outside the channel holds end portions of the guidewires. Pulling an end portion of one of the coiled guidewires horizontally causes the guidewire to slide along the inner wall for separation and removal from the storage tray.

A drain valve for a sterile container includes: a valve housing; a bypass that connects a container gas volume with an external gas volume; a valve body that blocks the bypass; and an actuator that displaces the valve body between a passage position and a blocking position. The valve body is displaceable according to a temperature and/or a pressure of the bypass gas volume. The valve housing has: at least one holding web, at least part of which can be located in a holding bracket of the valve receptacle; and a closure. The valve housing is pivotable from an open position into an installation position in which the closure can be fixed to a closure receptacle. When the valve housing is transferred into the installation position, the valve body is transferred into the blocking position and subjected to a closure force.

A sterilization packaging includes an interior space for receiving medical packaged goods and a sensor unit adapted to measure a first parameter in the interior space. The packaging has a data transmission unit for receiving and transmitting parameter values measured by the sensor unit. The packaging and data transmission unit are matched to one another to allow transmission of parameter values received by the data transmission unit into an outer space around the packaging. A sterilization method includes: introducing packaged goods into packaging and closing the packaging; introducing the closed packaging into a receiving chamber of a sterilizer; starting a sterilization process flow in the sterilizer; detecting parameter values in the packaging and transmitting the parameter values to a control unit of the sterilizer; and controlling the sterilization process flow as a function of the parameter values.

Packaging sleeve for medical purposes for storing sterile objects (25, 45), consisting of at least one outer sleeve (2) that is open at one end and can be sealed with a sealing closure (10) and has an inner sleeve (12) accommodated in it with a clamping effect, wherein the inner sleeve (12) is accommodated in a clamping seating in a receiving opening (15) in the sealing closure (10) on the bottom side of the outer sleeve (2) and the clamping seat thereby formed presses the sealing ribs (7, 55, 56, 59) arranged on the outside circumference of the sealing closure (10) against the inside of the outer sleeve (2) under increased contact pressure (FIG. 1).

The invention relates to a medical circulation detent device, comprising at least one circulation body and a latching element. The at least one circulation body comprising a restricted guide and at least one latching receptacle for the latching element. The latching element is guidable through the restricted guide from an unlatched position to a latched position at a first side of the at least one latching receptacle into the latter, and at a second side of the at least one latching receptacle from the latched position to an unlatched position again. An operative element is coupled to the latching element via a coupling element. A thermal actuating element is operatively connected to the latching element and transferable due to temperature from a first state to a second state and vice versa in order to move the operative element. The invention also relates to a medical sterilization container.

A method of applying a buttress to a surgically cut and stapled site uses an end effector with a buttress applier cartridge assembly to load one or more buttress assemblies to the end effector. The buttress assemblies each include a buttress to support a staple formed therein as well an adhesive for adhering to the end effector. The adhesive of the buttress assemblies can include a pattern to assist in both attachment to the end effector and release from the end effector after cutting and stapling a tissue site. The buttress applier cartridge can include features that accommodate end effectors having various tip configurations, including straight tips and curved or bent tips.