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Mechanical Walker Suppliers

 EMAIL INQUIRY to  221 to 223 of 223 suppliers  Page: << Previous 20 Results 10 11 [12]
Wolspal Inc. | Address: 4980 Rue Buchan Bureau 205, Montreal, Quebec H4P 1S8, Canada Canada
Phone: (514)-739-1310
Annual Revenues: < USD 1 Million
Products: Bed Transfer Aids, Transfer Aid for Disabled/Handicapped (FDA Code: IKX), Transfer Aid (FDA Code: IKX), Exercise Component (FDA Code: IOD), Disabled Grooming Adaptor (FDA Code: ILW), Homemaking Utensil (FDA Code: IKW), ...
Wolspal Inc. supplies surgical appliances. We specialize in the production of orthopedic appliances. more...
 
Walkerworks | Address: 4580 Hickmore St., Montreal, Quebec H4T 1K2, Canada Canada
Send Inquiry | Phone: (514)-344-3045, 800-667-4111
Products: Mechanical Walker (FDA Code: ITJ), ...
Walkerworks is a provider of walkers. Our Starfire walker, model WA300-C, is a folding adjustable walker designed with a removable basket and a seat for individuals who have difficulty walking without more...
A.M.G. Medical, Inc. | Address: 8505 Dalton Rd., Montreal, Quebec H4T-IV5, Canada Canada
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...
 EMAIL INQUIRY to  221 to 223 of 223 Mechanical Walker suppliers  Page: << Previous 20 Results 10 11 [12]
FDA Code / Regulation: ITJ / 890.3825

A mechanical walker is a four-legged device with a metal frame intended for medical purposes to provide moderate weight support while walking. It is used by disabled persons who lack strength, good balance, or endurance.

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.

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