An intelligent rechargeable battery pack having a battery management system for monitoring and controlling the charging and discharging of the battery pack is described. The battery management system includes primary and secondary protection circuits for monitoring the charging and discharging of the battery. Individual battery cells forming the battery pack are connected by a main bus to a connector for connection to a battery charger or a device to be powered, and the main bus may be interrupted by a switch controlled by the battery management system to prevent damage to the battery during charging or discharging of the battery.

Devices and methods for performing CPR on a patient within an imaging field of an imaging device. The device has a compression belt and a belt tensioning mechanism, both located on or in the device such that the head, neck, thorax and abdomen of the patient may be place within the imaging field with the compression belt installed about the patient and the belt tensioning mechanism will be located outside of the imaging field.

An elevation device used in the performance of cardiopulmonary resuscitation (CPR) and after resuscitation includes a base and an upper support operably coupled to the base. The upper support is configured to incline at an angle relative to the base to elevate an individual's upper back, shoulders and head. The elevation device includes a support arm coupled with the upper support. The support arm is movable to various positions relative to the upper support and is lockable at a fixed angle relative to the upper support such that the upper support and the support arm are movable as a single unit relative to the base while the support arm maintains the angle relative to the upper support. The elevation device also includes a chest compression device coupled with the support arm. The chest compression device is configured to compress the chest.

A system and method for mechanical CPR can include a device for providing compressive force to various locations on a patient, and biological monitoring systems to measure the effectiveness of the various locations of compressive force in pumping blood through the patient. The system can also include providing decompressive force to increase the efficacy of blood flow.

A direct, non-pharmaceutical, non-invasive method of enhancing neurophysiological and musculophysiological muscle performance, muscle rehabilitation and recovery in specific target muscle(s) in users. Use of the system may provide inhibition of spastic neurotransmission tremors. The device, system, and method utilizes direct vibration stimulation of the specific target through the use and application of a fabric/nylon sleeve or wrap shaped to conform to the extremity or joint, shoulder, neck or head on which the target resides. The device applies vibrations to the target muscle group(s) at up to 100 Hz, with the vibration generating motor mechanism contained within the fabric/nylon sleeve or wrap.

Embodiments disclosed herein relate to a garment system including at least one sensor and at least one actuator that operates responsive to sensing feedback from the at least one sensor to cause a flexible compression garment to selectively constrict or selectively dilate, thereby compressing or relieving compression against at least one body part of a subject. Such selective constriction or dilation can improve muscle functioning or joint functioning during use of motion-conducive equipment, such as an exercise bike or rowing machine.

A device for enhancing grip strength and forearm health of a user is disclosed herein. The device comprises a body in the form of a strap, a cuff disposed within a portion of the body, a tensioner comprising a rounded contact point and a threaded bolt. The device of the present invention allows a user to stretch and expand the fascia, allowing for blood to be increased in these muscles with less restriction.

Disclosed is a system and method for regulating tourniquet cuff pressure to restrict blood flow penetration past the cuff based on a personalized restrictive pressure (PRP). The system includes mechanisms for estimating a limb occlusion pressure (LOP) by determining a minimum pressure at which arterial blood penetration past an applied tourniquet cuff is stopped and measuring a pulsation characteristic associated with the LOP. Thereafter, the system establishes a PRP by determining a second pressure that restricts but does not stop arterial blood penetration past the cuff and that corresponds to a second pulsation characteristic differing by a percentage from the pulsation characteristic associated with the LOP. During a limb-activity time period, the system maintains pressure in the applied tourniquet cuff near the PRP, thereby restricting but not stopping arterial blood penetration past the cuff during the activity time period.

A perineum control device attachable to the user's undergarment, belt or similar clothing to apply pressure to the perineum to control various conditions including leakages of body fluids from the urethral, anal, and vaginal openings. The device and method comprise one or more front and rear retractors having a retractable cord supporting a bridge or band member positioned against a user's perineum. When a user puts on their undergarment, or tensioned and retractable cords exert a constant and predetermined upward compression force to an attached sanitary article (such as pads/napkins). The force pushes/pulls the article against the perineum increasing the perineum pressure above an abdominal or bladder pressure, which prevents or mitigates leakages and/or prolapses. The device keeps the article in constant close contact with the orifices of the perineum regardless of a user's vigorous movements and regardless of a user's body size, shape, and anatomical differences.

A compression garment apparatus for a body part of an human and/or animal having a flexible backing, attaching means, a segmented flex frame, and a shape memory alloy on the segmented flex frame. The shape memory alloy can be connected to two terminals on the frame forming a circuit. A controller can be connected to the terminals applying current to the shape memory alloy at defined intervals providing intermittent, sequenced, or continuous compression therapy.