A package (2; 3) for an object is provided having a bottom shell (21; 31); a top shell (22; 32) having a closure portion (24; 34) referred to as a “cap”, and a connection portion (23; 33) in the form of a hollow body and connected to the closure portion (24) by a hinge (25) to enable the closure portion (24; 34) to tilt relative to the connection portion (23; 33) in order to release access to the inside of the bottom shell (21; 31) through the connection portion (23; 33). The connection portion (23; 33) is provided with a stiffener element (290; 390) and a sealing strip (4; 4′) connects together the edges (241, 231) of the cap (24; 34) and of the connection portion (23; 33) that face each other over the entire length of said edges. Said connection portion (23; 33) of the top shell (22; 32) and of the bottom shell (21; 31) are two parts that are fastened to each other, preferably by bonding.

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.

The invention provides a packaging element (2, 3) comprising two shells (21, 22, 31, 32), each shell having a margin (210, 220) defining an access opening giving access to the inside of the shell, said packaging element (2, 3) having at least a “closed” configuration in which the shells form a chamber that is substantially closed and that is suitable for receiving an article, such as a medical implant. Said packaging element (2, 3) further comprises a sealing strip (4) that extends, outside the shells (21, 22, 31, 32), over the entire length of the margins (210, 220) of the shells of the packaging element, and from one margin (210, 220) of the shell to the other margin (220, 210) of the shell in such a manner as to seal the chamber defined by the two shells. The invention also provides an assembly comprising two packaging elements received one inside the other, and the invention also provides a corresponding sealing method.

A disposable pen needle, comprising a hub having a needle situated thereon having a patient end and a non-patient end, a removable patient end cap attached at the distal end of the hub, a removable non-patient end cap attached at the proximal end of the hub, wherein greater force is required to detach the patient end cap than is required to detach the non-patient end cap.

A packaging assembly may retain a sterile medical device for use in a surgical setting, such as an orthopedic implant or instrument. The packaging assembly may have a first packaging component and a second packaging component. The first packaging component and the second packaging component may be attachable to each other to define a first interior space containing the medical device. The first packaging component may have a first retention feature that defines a first interior receptacle shaped to receive at least part of the medical device such that a user can manually grip the medical device through the first retention feature. The first interior space may be manually opened by a user grasping the medical device through the first retention feature.

A surgical tool configured for operation in connection with a robotic system. The surgical tool includes a shaft and an end effector extending distally from the shaft. The end effector comprises a first jaw member and a second jaw member movable relative to the first jaw member from a closed position to an open position in response to at least one axial motion. In addition, the surgical tool includes a motor configured to generate at least one rotational motion and a motion conversion assembly operably coupled to the motor and the second jaw member, wherein the motion conversion assembly is configured to convert the at least one rotational motion to the at least one axial motion.

A surgical tool configured for operation in connection with a robotic system. The surgical tool includes a shaft and an end effector extending distally from the shaft. The end effector comprises a first jaw member and a second jaw member movable relative to the first jaw member from a closed position to an open position in response to at least one axial motion. In addition, the surgical tool includes a motor configured to generate at least one rotational motion and a motion conversion assembly operably coupled to the motor and the second jaw member, wherein the motion conversion assembly is configured to convert the at least one rotational motion to the at least one axial motion.

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.

The disclosure relates to an assembly for storing, dispensing, disposing, and shipping medical products such as sharps or pharmaceuticals. The assembly includes an outer container, an inner container, a unit configured for storing and dispensing unused medical products such as sharps or pharmaceuticals, and for receiving used medical sharps or unused pharmaceuticals. The inner container is adapted to receive the unit, and the outer container is adapted to receive the inner container.

A portable device and method of supplying power to the portable device may provide a sterile environment that may protect the health and safety of patients on whom the device is employed. The portable device may be charged inside of the sterile environment. The portable device may be charged using at least one chargeable battery that may be arranged internal and/or external to a portion of the portable device, or internal and/or external to the portable device. A power supply may be connected to the at least one chargeable battery and power the portable device for use. The portable device may be charged up to 100% and/or or fully charged prior to opening the sterile environment.