Non-Sterile Absorbent Tipped Applicator Suppliers
Phone: +1-(514)-6859966
FDA Registration: 3007616062
Products: Non-Sterile Absorbent Tipped Applicator (FDA Code: KXF), ...
Iris Beauty Supplies Inc. provides non-sterile absorbent tipped applicators. more...
www.amdritmed.com | Send Inquiry | Phone: +1-(888)-441-2120
Annual Revenues: USD 10-25 Million Quality: ISO 9002, CE Certified
Products: Cotton Sponges, Masks & Faceshields, General Medical Supplies, Procedure Kits & Packs, Conventional Cotton Sponges, Nonwoven Cotton Sponges, ...
Amd-Ritmed Inc. manufactures a full line of surgical dressings, as well as specialty products. All specialty surgical dressings are available strung or nonstrung, either mounted on count cards or in b more...
www.amgmedical.com | Send Inquiry | Phone: (514)-737-5251, 888-396-1213
FDA Registration: 8022077 Annual Revenues: USD 10-25 Million Employee Count: ~90
Products: Adhesive Strips & Patches, Skin Closure Adhesive Strips (FDA Code: FPX), Self Adhesive Strips (FDA Code: FPX), Alcohol Swabstick, Microfoam Adhesive Strip, Alcohol Swabs, ...
A.M.G. Medical, Inc. is a manufacturer and wholesale distributor of medical professional and home healthcare products. We are an ISO 9001 certified company, and licensed by Health Canada as well as re more...
www.sibelsa.be | Phone: 328-145-0459
Products: Wire Twisters (FDA Code: HXS), Automatic Wire Twisters, Surgical Instruments, Wire Twisters, Sternal Wire Twister, Disposable Electrosurgical Snare, Surgical Snare (FDA Code: GAE), ...
Simal Sa is a manufacturer of surgical instruments. Our products include micro scissors, tissue forceps, hemostatic forceps, clamping forceps, flat and round handle micro needle holders, bulldog & vas more...
An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.
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.
