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ENT Applicator Suppliers

 EMAIL INQUIRY to  41 to 42 of 42 suppliers  Page: << Previous 20 Results 1 2 [3]
Po Wah Co.,Ltd. | Address: 1/f.,Tung Lee Industrial Building, 9 Lai Yip St., Kwun Tong, Kowloon, Hong Kong, China China
Phone: +852-(283)-87667
FDA Registration: 1000539597
Products: Visual Acuity Charts (FDA Code: HOX), Non Dental Irrigating Syringe (FDA Code: KYZ), ENT Applicator (FDA Code: KCJ), Hemorrhoid Cushion (FDA Code: LRL), Solid Medication Dispenser (FDA Code: NXB), Pill Crusher/Cutter (FDA Code: OHY), ...
Po Wah Co.,Ltd deals with bite blocks, disabled grooming adaptors, ENT applicators, graduated liquid medication containers, hand splints and components. We offer hemorrhoid cushions, microscope slide more...
 
Across Medical Disposables Co., Ltd. | Address: 1, Shuanggang Road, Anqing, Anhui 246000, China China
www.acrossmed.com | Send Inquiry | Phone: +86-(556)-5190180/5190179
FDA Registration: 3004938767  Quality: ISO13485, ISO11135-1:2007, ISO11607 Certified
Products: Tongue Depressors (FDA Code: FMA), Infant Tongue Depressor (FDA Code: FMA), Adult Tongue Depressor (FDA Code: FMA), Junior Tongue Depressor (FDA Code: FMA), Non-Surgical Tongue Depressor (FDA Code: FMA), Sterile Absorbent Tipped Applicator (FDA Code: KXG), ...
Across Medical Disposables Co., Ltd. is a manufacturer of medical cotton tipped applicators. Our gloves include plastic and PVC gloves. Our cotton products are cotton pads, cotton wools and gauze band more...
 EMAIL INQUIRY to  41 to 42 of 42 ENT Applicator suppliers  Page: << Previous 20 Results 1 2 [3]
FDA Code / Regulation: KCJ / 874.5220

An ear, nose, and throat drug administration device is one of a group of ear, nose, and throat devices intended specifically to administer medicinal substances to treat ear, nose, and throat disorders. These instruments include the powder blower, dropper, ear wick, manual nebulizer pump, and nasal inhaler.

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

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