Non-Sterile External Non-Inflatable Extremity Splint Suppliers
Huai An Jmi Glove Manufacturing Co. | Address: No. 2, Dong San Street, Hong Ze Industrial Park, Huai An City, CN-32 223100, China 
Products: Disposable Syringes, Insulin Disposable Syringes Kits, Insulin Syringes, Scalp Vein Sets, Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
Huai An Jmi Glove Manufacturing Co. is a manufacturer of hand gloves. Our product line includes disposable syringes, gloves, insulin syringes, scalp vein sets and non-woven gloves. more...
Products: Disposable Syringes, Insulin Disposable Syringes Kits, Insulin Syringes, Scalp Vein Sets, Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
Huai An Jmi Glove Manufacturing Co. is a manufacturer of hand gloves. Our product line includes disposable syringes, gloves, insulin syringes, scalp vein sets and non-woven gloves. more...
Suzhou Connect Medical Technology Co., Ltd. | Address: Room 314 Tongding International B/d, 2518 Huayan Road, Wujiang, Jiangsu, CN-32 215200, China
FDA Registration: 3008111549
Products: Cast Bandage (FDA Code: ITG), Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
Suzhou Connect Medical Technology Co., Ltd. specializes in offering orthopedic fiberglass casting tape, splint and bandage. more...
FDA Registration: 3008111549
Products: Cast Bandage (FDA Code: ITG), Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
Suzhou Connect Medical Technology Co., Ltd. specializes in offering orthopedic fiberglass casting tape, splint and bandage. more...
Paratex Medical | Address: Room 207 Building 7 Liquan Riverside Gar, Luoxi New City Panyu District, Guanzhou, CN-44 511431, China
www.paratexmedical.com
Products: Forceps (FDA Code: HTD), Adhesive Bandages (FDA Code: KGX), Elastic Bandages (FDA Code: FQM), Scavenging Mask (FDA Code: KHA), Nonresorbable Gauze/sponge for External Use (FDA Code: NAB), Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
Paratex Medical manufacturers pre-hospital emergency medical equipment including first aid and paramedical equipments. Our products include first aid containers, paramedic bags, first aid kits and fir more...
www.paratexmedical.com
Products: Forceps (FDA Code: HTD), Adhesive Bandages (FDA Code: KGX), Elastic Bandages (FDA Code: FQM), Scavenging Mask (FDA Code: KHA), Nonresorbable Gauze/sponge for External Use (FDA Code: NAB), Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
Paratex Medical manufacturers pre-hospital emergency medical equipment including first aid and paramedical equipments. Our products include first aid containers, paramedic bags, first aid kits and fir more...
McArthur Medical Sales Inc. | Address: 1846 5th Concession West, P.O. Box 7, Rockton, Ontario L0R 1X0, Canada 
www.mcarthurmedical.com | Send Inquiry | Phone: +1-(519)-622-4030, 800-996-6674
FDA Registration: 9615334 Year Established: 1984
Products: Medical Support Stocking (FDA Code: FQL), Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
McArthur Medical Sales Inc. offers products for home and professional healthcare, personal fitness & asthma control. We offer various consumer products including dressing aids, suspension pads, asthma more...
www.mcarthurmedical.com | Send Inquiry | Phone: +1-(519)-622-4030, 800-996-6674
FDA Registration: 9615334 Year Established: 1984
Products: Medical Support Stocking (FDA Code: FQL), Non-Sterile External Non-Inflatable Extremity Splint (FDA Code: NOC), ...
McArthur Medical Sales Inc. offers products for home and professional healthcare, personal fitness & asthma control. We offer various consumer products including dressing aids, suspension pads, asthma more...
EMAIL INQUIRY to 41 to 44 of 44 Non-Sterile External Non-Inflatable Extremity Splint suppliers Page: 
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FDA Code / Regulation: NOC / 878.3910
A noninflatable extremity splint is a device intended to immobilize a limb or an extremity. It is not inflatable.
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 878.9. If the device is not labeled or otherwise represented as sterile, it is 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 of this chapter, with respect to general requirements concerning records, and 820.198 of this chapter, with respect to complaint files.
