A vein heating assembly includes a sleeve that has a first portion which is hingedly coupled to a second portion. The first portion is positionable in an open position to have a patient's arm positioned therein and the first portion is positionable in a closed position to surround the patient's arm. A plurality of nozzles is each integrated into the sleeve. A plurality of heating elements is each coupled to the sleeve to warm the patient's arm when the heating elements are turned on thereby increasing blood flow in the arm for enhancing the appearance of veins. A steam unit is integrated into the sleeve to produce steam that is delivered onto the patient's arm for increasing blood flow in the arm for enhancing the appearance of veins.

The embodiments herein provide a method for producing activated carbonaceous balls. The method includes a step of crushing and sizing raw coconut shells to form coconut shell granules having a diameter of about 0.02 mm-2.36 mm, preferably 0.075 mm-1.18 mm. The method includes a step of mixing pure water to a food grade powder appropriately and boiling it slowly at 15° C.-80° C. to obtain a water-food grade powder mixture. The method includes a step of adding the water-food grade powder mixture 20-40% by weight to the coconut shell granules 100% by weight to obtain a slurry in a pourability condition. The method includes a step of pouring the slurry into a pill making machine equipped with a mold of 3 mm, 5 mm, and 8 mm in diameters selectively to produce the spherical carbon tablets. The method includes a step of drying the spherical carbon tablets and carbonizing the spherical carbon tablets to obtain the activated carbonaceous balls.

The present disclosure relates to a functional joint assist apparatus including an air bladder having a cut hole and divided into a plurality of air cells so that air is injected into at least one of the air cells; and a fixing unit coupled to a front surface or a rear surface of the air bladder to attach or detach the air bladder to/from the joint.

In accordance with one embodiment, a uniform total body cryotherapy method and apparatus operative to allow an individual in a cryotherapy chamber to be subjected to the same cold temperatures on their entire body at the same time. In use, the apparatus allows active dissemination of cold air in a confined space without the undesired consequence of wind shear commonly caused by forced movement of cold air.

The present invention relates to a heating element composition, and a method of manufacturing an eye mask pack, which shows that a heating temperature is regular, and heat is uniformly generated, a heating pack is able to be worn in a state of coming into close contact even with a curved surface, a preservation period is long, and the heating temperature and time for which heat is generated can be adjusted minutely. Also, the present invention relates to a device of manufacturing an eye mask pack which is capable of manufacturing self-heating packs rapidly even without the use of nitrogen.

Provided are a vapor ablation apparatus, and heating control method, controller, apparatus, and medium thereof; the heating control method includes: monitoring the current water level, current pressure, and current in-generator temperature of a steam generator; controlling a heating apparatus according to the current water level, the current pressure, and the current in-generator temperature. The disclosure is capable of accurately, promptly, and effectively automatically meeting the needs of a steam generator during heating, and the control results have good stability.

A steam generator according to the present invention comprises a heat generating layer comprising an oxidizable metal, a carbon component, and water, a first water absorbent layer laminated on the heat generating layer and comprising a first water absorbent, a water absorbing sheet laminated on the first water absorbent layer, and a second water absorbent layer laminated on the water absorbing sheet and comprising a second water absorbent.

A steam therapy equipment including a vessel for heating a mixture of water and organic materials, a compressor to inject pressurized air into the vessel producing pressurized steam. The pressurized steam is conducted into the equipment via one or more valves. The therapy equipment is formed from at least one panel and may include a supporting frame. The therapy equipment includes a temperature sensor to measure the temperature inside the therapy equipment when pressurized steam is admitted via the valves. A patient enters the equipment and is exposed to the pressurized steam, causing dilation of the skin pores of the patient, whereby toxins are removed from the patient. One or more applicators may conduct pressurized steam to specific portions of the body of the patient. The patient may be provided with a portion of the mixture to consume as part of the steam therapy treatment.

A steam therapy equipment including a vessel for heating a mixture of water and organic materials, a compressor to inject pressurized air into the vessel producing pressurized steam. The pressurized steam is conducted into the equipment via one or more valves. The therapy equipment is formed from at least one panel and may include a supporting frame. The therapy equipment includes a temperature sensor to measure the temperature inside the therapy equipment when pressurized steam is admitted via the valves. A patient enters the equipment and is exposed to the pressurized steam, causing dilation of the skin pores of the patient, whereby toxins are removed from the patient. One or more applicators may conduct pressurized steam to specific portions of the body of the patient. The patient may be provided with a portion of the mixture to consume as part of the steam therapy treatment.

A method of controlling an infant care device includes identifying, via a location tracking system, a device location of the infant care device within a care facility by locating a device location tag on the infant care device, and also identifying any local clinician tags worn by a clinician within a predetermined area around the device location. The local clinician tags are compared to a list of authorized clinician tags to identify whether at least one local authorized clinician tag is within the predetermined area around the infant care device. User input is received at a user interface associated with the infant care device to modify operation of the infant care device. Operation of the infant care device is modified based on the user input only if at least one local authorized clinician tag is within the predetermined area around the infant care device at the time of receiving the user input.