There is provided a throwaway cuff cover capable of being used for all types of cuffs and performing triage at the same time. The cuff cover has a long main cover 20 which is wound around the upper arm of the human body and a sub-cover 30 shorter than the main cover 20, the sub-cover 30 being provided connectingly along one side of the main cover 20 and capable of being folded onto the main cover 20 side, and the cuff housing portions 21 and 31 are allotted to the main cover 20 and the sub-cover 30, respectively.

A system for diverting emboli within a patient can include a device that detects a presence of emboli in a first blood vessel of a patient. A compression member can be aligned with a second blood vessel of the patient when a collar supporting the compression member is positioned at least partially around a portion of the patient. In response to the detection device, a controller can actuate the compression member, when the presence of emboli is detected, from an unactuated state to an actuated state in which at least a portion of the compression member (i) is closer to the second blood vessel than while in the unactuated state and (ii) compresses and limits blood flow through the second blood vessel.

A system for diverting emboli within a patient can include a device that detects a presence of emboli in a first blood vessel of a patient. A compression member can be aligned with a second blood vessel of the patient when a collar supporting the compression member is positioned at least partially around a portion of the patient. In response to the detection device, a controller can actuate the compression member, when the presence of emboli is detected, from an unactuated state to an actuated state in which at least a portion of the compression member (i) is closer to the second blood vessel than while in the unactuated state and (ii) compresses and limits blood flow through the second blood vessel.

The invention relates to a compression unit adapted to be arranged around a patient's forearm to provide pressure to a radial artery puncture site, wherein the compression unit comprises a unit attachment band provided with a frame, and a compression element in the shape of an inflatable bladder, the compression element is further adapted to be arranged within said frame, such that when the compression unit is arranged around a patient's forearm, the compression element provides pressure to the puncture wound when the compression element is inflated. The invention also relates to a radial artery compression system.

A femoral compression device (11) for compressing a femoral artery (12) of a patient, having a base plate (13) provided with two opposing extensions, each of the two opposing extensions having a member for affixing a belt (14), which is adapted to be arranged around a patient's body, an inflatable air cushion (15), provided with a back plate (19), for compressive bearing against a puncture site, and a pump (16) connected to the inflatable air cushion for inflation of the air cushion. The femoral compression device further comprises a spacer (18) having a height and being adapted to be mounted between the inflatable air cushion and the base plate.

A femoral compression device (11) for compressing a femoral artery (12) of a patient, having a base plate (13) provided with two opposing extensions, each of the two opposing extensions having a member for affixing a belt (14), which is adapted to be arranged around a patient's body, an inflatable air cushion (15), provided with a back plate (19), for compressive bearing against a puncture site, and a pump (16) connected to the inflatable air cushion for inflation of the air cushion. The femoral compression device further comprises a spacer (18) having a height and being adapted to be mounted between the inflatable air cushion and the base plate.

The invention features methods and devices for controlling bleeding from blood vessels that may be damaged as a result of trauma or impact with an object, such as a bullet or shrapnel. The device may be wearable by a user and include one or more components, such as wound sealant and multiple inflatable balloons/bladders. The device may be integrated into a garment, e.g., a vest, jacket, trousers, or full body suit. Once triggered (automatically or manually), the device may be used to deliver wound sealant to a wound site and/or pressure to the wound site by selective inflation of one or more balloons over exsanguinating blood vessels that may be damaged, thereby stopping or minimizing the bleeding. Alternatively, or in addition, the device may be used to stabilize a wounded wearer for, e.g., transportation purposes, or to provide buoyancy. Devices of the invention may also be used as a blood pressure monitor, as a massaging device, and as a breast pump.

Devices and methods of the invention may also be used for repairing or stabilizing machines, such as vehicles (e.g., automobiles and boats).

An inflatable belt 100 for use in a BFR system with an outer belt material 102 hermetically sealed to an inner belt material 101 along a perimeter, thereby forming at least one inflatable chamber 103, the inflatable chamber having an input port 104 for accepting a gas into the chamber, the inflatable belt further comprising a first fastening means 110 in communication with the outer belt material, for attaching to a second fastening means 111 in communication with the outer belt material, thereby locking a circumference of the inflatable belt, when wrapped around a user's limb.

An inflatable belt 100 for use in a BFR system with an outer belt material 102 hermetically sealed to an inner belt material 101 along a perimeter, thereby forming at least one inflatable chamber 103, the inflatable chamber having an input port 104 for accepting a gas into the chamber, the inflatable belt further comprising a first fastening means 110 in communication with the outer belt material, for attaching to a second fastening means 111 in communication with the outer belt material, thereby locking a circumference of the inflatable belt, when wrapped around a user's limb.

An intravenous (IV) therapy system to facilitate the insertion of a catheter or another suitable IV device into a patient may include a band made of flexible material to be secured around a limb of a patient. The IV therapy system may include a window formed through the band to provide access to the patient's body. The IV therapy system may include a tourniquet formed within the band to selectively apply a pressure against the patient's body. The IV therapy system may include a blood vessel indicator to indicate where the catheter or other suitable IV device is to be inserted.