A disposable, sterile guide constructed of medically-acceptable plastic used for compartmentalizing and therefore protecting the ligament or fascia during three different orthopedic surgical procedures: ECTR, ECuTR, and EPFR. This device reduces the risk of damage to any other part of the surrounding anatomy. The device is disposable and packaged so as to be sterile and therefore readily usable by the surgeon means that it can reduce the risk of infection and is a less expensive alternative to traditional non-disposable, metal instruments that must be sterilized prior to each procedure.

A blade disarmer is provided herein. The blade disarmer includes a base member having an elongated portion, a bottom portion, and first and second walls extending from the elongated portion. A cover member is removably attached to the base member forming a cavity therebetween. The cover member includes a hinge separating a body portion and a tab. A pair of dome-shaped portions is disposed on the tab configured to assist a pair of side surfaces of the tab proximate each respective dome-shaped portion to flex laterally. A closure mechanism is disposed on the first and second walls and configured to maintain the tab in a plurality of positions. First and second protrusions extend into the cavity.

A disposable container (1, 1, 1), in particular for the disposal of sharp medical waste is provided, comprising a first opening (13, 13) sealingly closable by a cover element (2), characterized in that the container is manufactured by blow-moulding; the largest cross-sectional diagonal of the container in the distal half with respect to the first opening is larger than the smallest cross-sectional diagonal of the container in the proximal half with respect to the first opening; and the container comprises a second opening (15, 15) arranged opposite to the first opening or in the distal area with respect to the first opening, the second opening being sealingly closable by a base element (11, 11).

A disposable container (1, 1, 1), in particular for the disposal of sharp medical waste is provided, comprising a first opening (13, 13) sealingly closable by a cover element (2), characterized in that the container is manufactured by blow-moulding; the largest cross-sectional diagonal of the container in the distal half with respect to the first opening is larger than the smallest cross-sectional diagonal of the container in the proximal half with respect to the first opening; and the container comprises a second opening (15, 15) arranged opposite to the first opening or in the distal area with respect to the first opening, the second opening being sealingly closable by a base element (11, 11).

According to the invention, there is provided a medical apparatus comprising: one or more sterile pre-filled syringe; one or more first protective container comprising the one or more sterile pre-filled syringe, wherein the one or more first protective container is impermeable to moisture and/or sterilizing agents; a second protective container comprising one or more medical components and the one or more first protective container; and a package impermeable to bacteria comprising the second protective container.

According to the invention, there is provided a medical apparatus comprising: one or more sterile pre-filled syringe; one or more first protective container comprising the one or more sterile pre-filled syringe, wherein the one or more first protective container is impermeable to moisture and/or sterilizing agents; a second protective container comprising one or more medical components and the one or more first protective container; and a package impermeable to bacteria comprising the second protective container.

A hemostatic device is provided to stop bleeding at a puncture site on the wrist of a patient, the device comprising a transparent flexible band to be wrapped at the site where the bleeding is to be stopped, a curved frame having an inner peripheral side and possessing a first curved portion in its first half and a second curved portion in its second half, a first balloon provided on the inner peripheral side in the first half of the curved frame and a second balloon provided on the inner peripheral side in the second half of the curved frame. The bleeding from a first artery is stopped by compressing the first artery at the puncture site using inflation of the first balloon and the blood flow in the first artery is increased by compression of a second artery using inflation of the second balloon.

The present invention is directed to a Point Specific Junctional Tourniquet Kit designed for the treatment of hemorrhage control of junctional injuries to a patient's torso especially in the area of the iliac (hip/groin area) and axillary (shoulder/armpit area) arteries where blood flow is extremely hard to stop. The complete kit contains a variety of components to give caregivers in the military as well as civilian medical caregivers a means for treating a wide variety of severe injuries, in the pre-ambulance environment, increasing the chances of a victim surviving and reaching a higher level of care.

The present invention is directed to a Point Specific Junctional Tourniquet Kit designed for the treatment of hemorrhage control of junctional injuries to a patient's torso especially in the area of the iliac (hip/groin area) and axillary (shoulder/armpit area) arteries where blood flow is extremely hard to stop. The complete kit contains a variety of components to give caregivers in the military as well as civilian medical caregivers a means for treating a wide variety of severe injuries, in the pre-ambulance environment, increasing the chances of a victim surviving and reaching a higher level of care.

A method for mounting a tool to a surgical device using a packaging body. A proximal section of the packaging body is articulated about a second boundary relative to a first distal section of the packaging body for removing a proximal end of the tool from a proximal cavity for exposing the proximal end. The proximal end is mounted to the surgical device while a distal end of the tool remains securely retained by first and second distal sections of the packaging body within a distal cavity. After mounting, the distal end is released from the distal cavity by articulating one distal section relative to the other distal section for exposing a first portion of the distal end that was retained by the one distal section. Thereafter, the other distal section is removed for exposing a remaining portion of the distal end that was retained by the other distal section.