Crutch and Walker Cane Tips Suppliers
www.taft.com.cn | Send Inquiry | Phone: +86-(592)-5258462
FDA Registration: 3006799874
Products: Adjustable Hospital AC-Powered Beds (FDA Code: FNL), Non AC-Powered Patient Lift (FDA Code: FSA), Disabled/Handicapped Hygiene Adaptor (FDA Code: ILS), Mechanical Table (FDA Code: INW), Mechanical Walker (FDA Code: ITJ), Wheelchair Component (FDA Code: KNN), ...
Xiamen Taft Medical Co., Ltd. provides mechanical wheelchairs, handicapped canes, powered wheelchairs, manual beds, air flotation mattress and alternating pressure air flotation mattress. more...
www.alphaprotech.com | Send Inquiry | Phone: +1-(520)-281-0127
Year Established: 1993 Annual Revenues: USD 1-5 Million Employee Count: ~450 Quality: CE Certified
Products: Coats, Jackets & Smocks, Masks & Faceshields, General EMT, General Medical Supplies, Patient Examination Gowns & Capes, Examination Gown (FDA Code: FME), ...
Alpha Pro Tech Inc. renders innovative solutions for healthcare, industrial safety and laboratories. We manufacture & market disposable protective apparel and face masks. The PFL® N-95 particulate more...
www.amgmedical.com | Send Inquiry | Phone: (514)-737-5251, 888-396-1213
FDA Registration: 8022077 Annual Revenues: USD 10-25 Million Employee Count: ~90
Products: Adhesive Strips & Patches, Skin Closure Adhesive Strips (FDA Code: FPX), Self Adhesive Strips (FDA Code: FPX), Alcohol Swabstick, Microfoam Adhesive Strip, Alcohol Swabs, ...
A.M.G. Medical, Inc. is a manufacturer and wholesale distributor of medical professional and home healthcare products. We are an ISO 9001 certified company, and licensed by Health Canada as well as re more...
Cane, crutch, and walker tips and pads are rubber (or rubber substitute) device accessories intended for medical purposes that are applied to the ground end of mobility aids to prevent skidding or that are applied to the body contact area of the device for comfort or as an aid in using an ambulatory assist device.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 890.9. The device is also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, regarding general requirements concerning records and 820.198, regarding complaint files.
