In an aspect, a method of manufacturing a surgical kit includes providing one or more medical devices based on a three-dimensional (3D) image of an anatomical structure. The method additionally includes providing packaging based on the 3D image, and providing the surgical kit utilizing the packaging and the one or more medical devices. In another aspect, a surgical kit has one or more contoured packaging surface having a contour that matches a contour of an anatomical structure. The contoured packaging surface has one or more features for receiving one or more medical devices provided based on the contour in the 3D image. The surgical kit additionally has a lid connected under pressure with the one or more contoured packaging surface. The lid has apertures for sterilization of components of the one or more medical devices situated between the lid and the contoured packaging surface.

An apparatus including a sterilizable tray having a base and at least one fixture connected to the tray adapted for removably securing an implant insertion device to the tray. The tray can be free of a first wall portion for permitting the proximal end of an implantable device to axially align with the end of the implant insertion device for coupling to the implant insertion device and can be free of a second wall portion for permitting a tool to axially align with the end of the implant insertion device so as to threadedly couple the implant insertion device to the implantable device. Related methods and apparatus are provided.

Surgical instrument trays and related methods are described. The surgical instrument tray is for a surgical instrument having a plurality of parts from which the surgical instrument is assembled. The surgical tray comprises a tray having a plurality of side walls and a base which define an interior space; a lid for closing the interior space and which is removable from the tray; and a plurality of outlines located within the interior space. Each outline has the shape of a corresponding different part of the surgical instrument and each outline has at least one support arranged to receive and releasably hold the respective different parts of the surgical instrument above and in registration with the outline. The plurality of outlines are configured to indicate that the different parts of the surgical instrument are assembled to form the surgical instrument and/or that the surgical instrument is disassembled into the different parts.

A method of operating a surgical system including an endoscope, a treatment tool, an overtube, and a sheathing tube. The method includes the following steps: removing the treatment tool from the sheathing tube inserted into a body cavity through a body wall in a state where the sheathing tube is covering an outer circumference of the overtube into which an insertion part of the endoscope and an insertion part of the treatment tool are inserted, while keeping a state where the sheathing tube is covering the outer circumference of the overtube; removing the endoscope from the overtube while keeping a state where the sheathing tube is covering the outer circumference of the overtube; and removing the sheathing tube from the body wall while keeping a state where the sheathing tube is covering the outer circumference of the overtube.

Embodiments of the disclosures made herein are directed to facilitating adjustability of operative apparatuses. More specifically, embodiments of the disclosures made herein are directed to mitigating adverse implications of having to adjust a control portion of an operative apparatus to a user-defined setting that is not otherwise a predefined setting position of the control portion. Such adverse implications may arise, for example, due to the time required for performing such adjustment with a required degree of precision. Thereby, such embodiments serve to mitigate, if not eliminate, that manner in which adjusting the control portion of the operative apparatus to the user-defined setting during a procedure can undesirably and/or unacceptably limit efficiency and/or effectiveness of the procedure.

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.

The present invention discloses a package for a capsule endoscope. The package includes an inner package. The inner package includes a base and a cover arranged above the base. A first end of the cover is connected to a first side of the base and a second end of the cover is connected to a second side of the base in an assembled mode. When the second end of the cover is assembled and connected to the second side of the base, the bottom surface of the cover and the base form an holding slot for holding the capsule endoscope. Through such arrangement, the present invention improves the existing package and avoids a reduction of performance of the capsule endoscope during transportation.

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.

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.

A medical package containing a medical article, including: a support element comprising a hollow support tube and a support cap, wherein the support element includes a first chamber configured to enclose the medical article and wherein the support cap includes a support structure configured to hold the medical article captive; a stopper configured to be coupled to the hollow support tube in such a way that the support element has a grip part that protrudes from the stopper, the grip part of the support element configured to be held by a hand of a person; a hollow protective cover configured to be coupled to the stopper in such a way as to delimit, in cooperation with the stopper, a second chamber inside which there extends the grip part of the support element, the hollow protective cover configured to be separated from the stopper, wherein when the hollow protective cover is coupled to the stopper, a part of the stopper protrudes from the hollow protective cover, and is configured to form a grip end of the stopper that is configured to be held by a hand of a person, when the hollow protective cover is separated from the stopper, wherein a part of the support element is configured to be engaged by force inside the stopper, and when the hollow protective cover is separated from the stopper, the support element remains coupled to the stopper while the support element is also separable from the stopper when a person holds the grip part of the support element and pulls the support element so as to separate it from the stopper.