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Ear Irrigation Kit Suppliers

 EMAIL INQUIRY to  3 suppliers  
Oto-Med, Inc. | Address: 1090 Empire Dr., Lake Havasu City, Arizona 86404, USA USA
www.otomed.com | Send Inquiry | Phone: +1-(800)-433-7703
FDA Registration: 2021687  Year Established: 1972  Annual Revenues: USD 1-5 Million
Products: Insufflators, Ear Wick (FDA Code: KCN), Patient Eye Protectors, Ear Plug, Instrument Wipe, Ear Irrigation Kit (FDA Code: OGQ), ...
Oto-Med, Inc. specializes in otorhinolaryngology. Our product index comprises of ventilation tubes, surgical accessories, surgical dressings, and surgical sponges. Our ear wicks are ideal for maintain more...
 
Ethicare Products | Address: P.O. Box 5027, Fort Lauderdale, Florida 33310-5027, USA USA
www.ethicare.com | Send Inquiry | Phone: +1-(954)-742-3599, 800-253-3599
Annual Revenues: < USD 1 Million
Products: Razors, Safety Razors, Ear Irrigation Kit (FDA Code: OGQ), ENT Lavage Unit, Powered Nasal Irrigator (FDA Code: KMA), Sinus Irrigator (FDA Code: KAR), ...
Ethicare Products provides nasal irrigators for nasal congestion and sinus problems. Our products are Sinus Rinse™, Hydro-Flo™ and Shavever™. The Hydro-Flo unit provides a steady flo more...
Centurion Medical Products | Address: 301 Catrell Drive, Howell, Michigan 48843, USA USA
www.tshsc.com | Send Inquiry | Phone: +1-(516)-546-5400, 800-248-4058
FDA Registration: 1824619  Year Established: 1961  Employee Count: ~720  Quality: ISO 9000, ISO 9001, CE Certified
Products: Scissors, Iris Scissors, Gauze Dressings, Hemostats, Island Dressings, Labels & Signs, ...
Centurion Medical Products provides a variety of custom procedure kits, trays and specialty products to hospitals, health care facilities, non acute alternate site & home care providers. All our facil more...
 EMAIL INQUIRY to  3 Ear Irrigation Kit suppliers  
FDA Code / Regulation: OGQ / 880.6960

An irrigating syringe is a device intended for medical purposes that consists of a bulb or a piston syringe with an integral or a detachable tube. The device is used to irrigate, withdraw fluid from, or instill fluid into, a body cavity or wound.

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 880.9. If the device is not labeled or otherwise represented as sterile, it 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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