A61H9/005

AIR BAG AND MASSAGE MACHINE

A primary object of the present invention is to provide an air bag and a massage machine which can allow a person to select one of an appropriate pressure massage and an appropriate massage with an air bag. An arm air bag portion 600 includes base bodies 610, 620 each containing a frame and a resin molding product, one or more protruding portions 630 for pressure provided on the base bodies 610, 620 and one or more expansion and contraction bags 640, 650, 660, 670, 690 provided on the base bodies 610, 620 and provided around the one or more protruding portions 630 for pressure. An expansion height of each of the one or more expansion and contraction bags 640, 650, 660, 670, 690 is higher than a protruding height H of each of the one or more protruding portions.

PATIENT SUPPORT APPARATUS HAVING AN INTEGRATED LIMB COMPRESSION DEVICE

A patient support apparatus includes a frame having a patient support deck. A footboard is removably coupled to the frame. A compression therapy module is located inside the footboard or is mounted to a foot section of the frame. A sleeve port is pneumatically coupled to the compression therapy module and is located on the foot section. The sleeve port is configured for attachment to at least one tube extending from a compression sleeve worn on a limb of a patient. Control circuitry is coupled to the frame and is operable to control functions of the patient support apparatus and to control the compression therapy module. A graphical display screen is coupled to the control circuitry and displays user inputs that are selected to control functions of the patient support apparatus and the compression therapy module.

MASSAGE APPARATUS
20170231861 · 2017-08-17 · ·

A massage apparatus including: a base; a pair of air bags including a first air bag and a second air bag, the first air bag and the second air bag being vertically overlapped while being displaced from each other, the first air bag being disposed on an upper side of the second air bag, and the first air bag and the second air bag being joined to each other at an overlapped site; and an air injection and discharge section arranged to be connected to the first air bag, inject air into the first air bag, and discharge the air from the first air bag, wherein a coupling section including a through hole arranged to communicate the pair of air bags with each other is provided at a site where the pair of air bags is joined to each other, and a fixing section arranged to rotatably fix the first air bag to the base is provided in a portion of the first air bag, the portion being not overlapped with the second air bag.

MASSAGE APPARATUS COMPRISING A STACK OF INFLATABLE AND DEFLATABLE CELLS INCLINED AND OVERLAPPING ONE ANOTHER
20170224577 · 2017-08-10 ·

A pressotherapy apparatus including a device for forming a treatment enclosure to be placed around a section of the body. The device has inflatable and deflatable cells having an upper membrane and a lower membrane which are connected together. The cells are supported by an external wall opposite a body surface of the device. The cells are disposed in a stack between two end cells. The cells between the end cells are stacked by overlapping in a position inclined between a high-end near to the external wall and a low end near to the body surface. The cells of the stack have an active portion of the upper membrane extending from the low end not covered by the lower membrane of an adjacent cell above.

THERAPEUTIC MASSAGE SYSTEM
20220031557 · 2022-02-03 · ·

A therapeutic massage system is provided. The system is characterized by a controllable compressed air delivery system and a cushion adapted for operative union with a portion of the air delivery system. The cushion includes a support pad and a therapy pad, the support pad having head and vertebral column supporting portions. The support pad vertebral column supporting portion is characterized by longitudinally extending compartments containing filler material. A central compartment of compartments of the support vertebral column supporting portion having a primary region traversing an axial centerline of said cushion and secondary regions spaced apart from said primary central region. The therapy pad overlays and is affixed to the vertebral column supporting portion of the support pad, the therapy pad including a plurality of fluid fillable channels for receiving a vertebral column wherein select fluid fillable channels of the plurality of fluid fillable channels of the therapy pad are fillable via programmed actuation of an actuatable element of the air delivery system. Filler material of the compartments of the support vertebral column supporting portion are responsive to receipt of body weight upon the cushion and select filling of the plurality of fluid fillable channels of the therapy pad, filler material of the regions of the central compartment being passable throughout segments of same in response to receipt of body weight upon the cushion and select filling of the plurality of fluid fillable channels of the therapy pad.

Methods of diagnosing and treating neonatal reversion to fetal consciousness

This invention provides methods of diagnosing and treating syndromes of reversion to fetal consciousness in a neonate.

MEDICATED THREAD DRAINAGE THERAPY APPARATUS
20220265476 · 2022-08-25 ·

The present disclosure belongs to the field of treatment devices, and specifically relates to a medicated thread drainage treatment device. The treatment device includes a first treatment unit used for postoperative pain relief and drainage; a second treatment unit used for promoting quick healing of a wound; a third treatment unit used for preventing deep venous thrombosis; and an electropneumatic, negative-pressure, electric stimulation multipurpose therapy apparatus connected with the first treatment unit, the second treatment unit, and the third treatment unit and providing electropneumatic pressure, negative pressure, and electric energy. The present disclosure is used for postoperative quick healing and recovery; promotion of clinical use guidelines will greatly reduce and even eliminate the postoperative complications, particularly postoperative complications of pulmonary embolism, thus saving patients' lives.

Ear pumps

A manual ear pump including one or more of a support element configured to releasably engage an external ear canal and having an interior chamber, a resilient element capable of being resiliently deformed coupled to a support element, and an aperture disposed on a support element bottom surface communicating with the external ear canal and interior chamber.

FLUID PATH INSPECTION DEVICE AND FLUID PATH INSPECTION METHOD

There are provided a fluid-path tester and a fluid-path testing-method capable of performing classification of abnormal-modes into a problem in a system, a leakage in a dedicated tube, a problem of a failure in a suppression pressure, and the like, an analysis of the abnormal-modes, and the like in a simplified manner. PAPS valves are included, and an abnormality emulator inspecting an abnormal condition in a fluid path of a DUT by emulating characteristics of the fluid-circuit represented by each of a plurality of abnormal-modes having possibilities of occurring in the fluid path of the DUT through pressurization of a fluid pressure using a compressor-under-test and adjustment of the fluid pressure using the PAPS valves.

Compression Wave Massage Device
20220233395 · 2022-07-28 · ·

A compression wave massage device for body parts is described, particularly for erogenous zones such as the clitoris, comprising a pressure field generation device and a drive device. The pressure field generation device has at least one cavity with a first end and a second end, located opposite the first end and distanced from said first end, with the first end being provided with at least one opening for placement on a body part. The drive device causes a change of the volume of at least one cavity between a minimal volume and a maximal volume such that in at least one opening a stimulating pressure field is generated. The cavity is formed by a single chamber, and the ratio of the volume change to the minimal volume is not below 1/10, preferably not below ⅛.