Medical device kits for use in placing, maintaining, altering, and/or removing medical devices in, on, and/or from the body of a patient can include one or more wrap assemblies for use in the placement/maintenance procedure. The one or more wrap assemblies of the medical device kit can include various features to assist the clinician performing the particular procedure, such as a urinary catheterization procedure. A wrap assembly can include a wrap body including a front surface defining an aseptic field for the urinary catheterization procedure, a plurality of pockets on the front surface, and urinary catheterization components disposed in the plurality of pockets, the urinary catheterization components arranged in a predetermined order of use for the urinary catheterization procedure. The wrap assembly can be in a rolled configuration. A method of using the wrap assembly includes unrolling the wrap assembly and removing the urinary catheterization components to perform the procedure.

A medical instrument holder including a sheet with front and rear faces and first and second ends. A first pocket is formed on the rear face at the first end and has a mouth which is open towards the second end. A second pocket is formed on the front face at the second end and comprises a mouth which is open towards the first end. An instrument tray is attached to the sheet on the front face at the first end, opposite to the first pocket.

Many variations of systems, methods and apparatus for counting medical procedure objects, reconciling same, estimating patient blood loss during and/or after a procedure, and/or communicating between medical equipment used in a medical procedure setting are disclosed and/or illustrated herein. More particularly, many systems, methods and apparatus for counting and/or reconciling medical sponges with passive or active tracking devices, properly detecting/estimating blood loss during and/or after a medical procedure to assist with transfusion decision-making and identifying or at least alerting as to post-procedure patient risks, and/or for communicating between devices used during procedures to provide a smart/connected medical procedure environment are disclosed and/or illustrated herein.

Systems and methods are provided for syringe organization including a backing, a plurality of pockets coupled to the backing and a coordination scheme indicating the contents of individual pockets.

An embodiment of the invention provides a trauma kit including a plurality of medical packets, wherein one or more of the medical packets includes treatment instructions, a first tool for treating a medical situation, the first tool being labeled in a first color, and a second tool for treating the medical situation, the second tool being labeled in a second color. The treatment instructions include a first treatment instruction labeled with a first character designated in the first color, and a second treatment instruction labeled with a second character designated in the second color. A treatment sequence chart includes a flow diagram of treatment steps, wherein each of the treatment steps are color-coded to one of the medical packets.

A single use container (10, 40, 70) for holding a plurality of endoscope valves during a cleaning and disinfection procedure defines a plurality of chambers (34, 64, 84) which are isolated from each other and configured to receive a single valve such that a valve in one chamber cannot contact a valve in another chamber. A plurality of apertures (36, 58, 86) in each chamber allow fluid flow therethrough. A closure device (14, 44, 92) is operable to close each chamber (34, 64, 84). An attachment device (38, 68, 77) is configured for attaching the container (10, 40, 70) to an endoscope and to prevent detachment without breaking of the attachment device (38, 68, 77).

A packaging assembly for a medical device includes at least one pouch, such as a first pouch and a second pouch, sealed so as to provide a sterile barrier between the environment and the medical device received in the first pouch, which in turn is received in the second pouch. The packaging assembly further includes at least one support member, wherein, in an assembled configuration, at least the first pouch and the support member are secured against movement relative to each other by at least one of the first and second pouches being folded around the support member. The at least one of the first and second pouches is folded around the support member such that at least the first pouch and the support member are secured against movement relative to each other, either before or after inserting the first pouch with the medical device into the second pouch. The support member may hold the packaging assembly within a secondary packaging, which corresponds in size and shape to the packaging assembly.

Many variations of systems, methods and apparatus for counting medical procedure objects, reconciling same, estimating patient blood loss during and/or after a procedure, and/or communicating between medical equipment used in a medical procedure setting are disclosed and/or illustrated herein. More particularly, many systems, methods and apparatus for counting and/or reconciling medical sponges with passive or active tracking devices, properly detecting/estimating blood loss during and/or after a medical procedure to assist with transfusion decision-making and identifying or at least alerting as to post-procedure patient risks, and/or for communicating between devices used during procedures to provide a smart/connected medical procedure environment are disclosed and/or illustrated herein.

A continuous process for making a multi-panel sterilization assembly, the process including the steps of: providing a moving, continuous base web; providing a plurality of subassemblies; applying the subassemblies in position on the moving, continuous base web to define repeating portions that incorporate the subassemblies and alternating portions that lack such subassemblies; providing side tabs; applying the side tabs in position on the moving, continuous base web with respect to at least one edge of the portions that incorporate the subassemblies; attaching the subassemblies and the side tabs to the moving, continuous base web to form a continuous work-piece; and separating the continuous work-piece into individual multi-panel sterilization assemblies, each multi-panel sterilization assembly comprising a barrier panel, a fold protection panel and at least one side tab.

A multi packaging system for packaging of sterile implants includes a carrier plate and a plurality of packings removably attached to the carrier plate. Each of the plurality of packings contains an implant and is individually removable from the carrier plate.