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Radiographic Head Holder Suppliers

 EMAIL INQUIRY to  21 to 23 of 23 suppliers  Page: << Previous 20 Results 1 [2]
Klarity Medical & Equipment Co., Ltd. | Address: 4 Fl., 1st Bldg. Guangzhou, Scienctech Park, No.9, Lan Yu, 4th Rd., Getdd, Guangzhou 510730, China China
www.klarity-medical.com | Send Inquiry | Phone: +86-(20)-82226380
FDA Registration: 3003803149  Quality: ISO 9001, ISO 13485 Certified
Products: Medical Thermometers, Nasal Splints (FDA Code: EPP), Plastic Splints, Hand Splint and Component (FDA Code: ILH), Medical Linear Accelerator (FDA Code: IYE), Splint Wraps, ...
Klarity Medical & Equipment Co., Ltd. deals with medical thermoplastic products. We provide medical splint that includes Contour Color™, Klarity Pro™ and Contour Pro™ splints. Our Kl more...
 
Shanghai Youjia Medical Supply Co., Ltd. | Address: 509 Yuzhuang Road, Shanghai 201414, China China
www.ukast.com | Send Inquiry | Phone: +86-(21)-57569919
Products: Plaster Bandages, Plaster Of Paris Bandages (P.O.P. Bandages), Plaster Casts, Cotton Rolls, Orthopedic Casting Tape, Cast Bandage (FDA Code: ITG), ...
Shanghai Youjia Medical Supply Co., Ltd. manufactures and supplies orthopedic casting products. Our products include POP bandage, sprint roll and casting tape. The U-Kast™ plaster bandage featur more...
Xinjiang Renfu Medical Equipment Co., Ltd. | Address: No.1 Donghuan Road, Urumchi, CN-65 830001, China China
FDA Registration: 3008494323
Products: Nasal Splints (FDA Code: EPP), Hand Splint and Component (FDA Code: ILH), Radiographic Head Holder (FDA Code: IWY), ...
Xinjiang Renfu Medical Equipment Co., Ltd. specializes in offering radiographic head holder. more...
 EMAIL INQUIRY to  21 to 23 of 23 Radiographic Head Holder suppliers  Page: << Previous 20 Results 1 [2]
FDA Code / Regulation: IWY / 892.1920

A radiographic head holder is a device intended to position the patient's head during a radiographic procedure.

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 892.9. 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, with respect to general requirements concerning records, and 820.198, with respect to complaint files.

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