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ENT Irrigation Syringe Suppliers

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 EMAIL INQUIRY to  121 to 126 of 126 suppliers  Page: << Previous 20 Results 1 2 3 4 5 6 [7]
Da Peng Cibo Plastic Factory | Address: Da Peng Town, Bao An, Shenzhen, China China
Products: ENT Syringe (FDA Code: KCP), ENT Irrigation Syringe (FDA Code: KCP), Liquid Medication Dispenser (FDA Code: KYX), ...
Da Peng Cibo Plastic Factory deals with medicine feeders and nasal aspirators. more...
 
Guangdong Intmed Medical Appliance Co., Ltd. | Address: 3rd Part, Europe Industry Park. South Shunhe Rd., Shunde District, Shunde 510520, China China
www.intmed.com.cn | Phone: +86-(757)-22915009
FDA Registration: 3005202238  Quality: ISO9001 and ISO13488 Certified
Products: ENT Syringe (FDA Code: KCP), Piston Syringe (FDA Code: FMF), ENT Irrigation Syringe (FDA Code: KCP), Non Dental Irrigating Syringe (FDA Code: KYZ), Antistick Syringe (FDA Code: MEG), Single Lumen Hypodermic Needle (FDA Code: FMI), ...
Guangdong Intmed Medical Appliance Co., Ltd. manufactures medical disposable products. Our products are disposable sterilized syringes, disposable self-destroyable syringes, disposable infusion sets, more...
Suzhou Jingle Polymer Medical Apparatus Co., Ltd. | Address: No. 18 Yingbin Rd, New District, Suzhou, China China
Phone: +86-(847)-6820224
FDA Registration: 3006536657
Products: Forceps (FDA Code: HTD), ENT Syringe (FDA Code: KCP), Piston Syringe (FDA Code: FMF), ENT Irrigation Syringe (FDA Code: KCP), Non-Invasive Tubing (FDA Code: GAZ), Single Lumen Hypodermic Needle (FDA Code: FMI), ...
Suzhou Jingle Polymer Medical Apparatus Co., Ltd. deals with forceps, needles, piston syringes, control syringes and silicone bulbs. We also offer ear/ulcer syringe, suction tubing, suction connecting more...
Elung Industrial Co.Ltd. | Address: Suite 507, Silvercord, Tower 1, 30 Canton Road, T.S.T.,Kowloon, Hong Kong, China China
Phone: +852-(236)-85328
Products: ENT Syringe (FDA Code: KCP), ENT Irrigation Syringe (FDA Code: KCP), Non Dental Irrigating Syringe (FDA Code: KYZ), Continuous Electronic Thermometer (FDA Code: FLL), Liquid Medication Dispenser (FDA Code: KYX), Reusable Hot /Cold Pack (FDA Code: IME), ...
Elung Industrial Co.Ltd. is a manufacturer of breast soothing pads, teething rings, nasal aspirator and thermometers. more...
New Prokin International Ltd. | Address: 6TH BLOG., 1ST IND.AREA-DONGQU,NO.12,ZHONGSHAN 5 RD, ZHONGSHAN 528400, China China
www.newprokin.com | Send Inquiry | Phone: +86-(760)-88321570
FDA Registration: 3005613467  Quality: ISO 9001 Certified
Products: Baby Care Items, Baby Care Accessories, Rehabilitation Equipment, Patient Lifts And Slings, Replacement Patient Lift-Slings, Patient Room Accessories, Lift Slings, Non AC-Powered Patient Lift (FDA Code: FSA), ...
New Prokin International Ltd. specializes in the production of medical, water proof and baby care products. Our patient slings are designed specially to support the patient during lift and transfer pr more...
Instrumentation difra S.A. | Address: 84, Rue De L'Eglise, Welkenraedt 4840, Belgium
Phone: +32-(87)-898080
Products: ENT Syringe (FDA Code: KCP), Ear Syringes Repair Service, Rhinomanometer, Baby Ear Syringe, Electric Ear Syringe, ENT Irrigation Syringe (FDA Code: KCP), ...
Instrumentation difra S.A. provides caloric water stimulators, therapeutic vestibular acceleration stimulators, ENT syringes and rhinomanometers. more...
 EMAIL INQUIRY to  121 to 126 of 126 ENT Irrigation Syringe suppliers  Page: << Previous 20 Results 1 2 3 4 5 6 [7]
FDA Code / Regulation: KCP / 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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