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U.S. FDA Medical Device Medical Absorbent Fiber Requirements


FDA Medical Device Definition: A medical absorbent fiber is a device intended for medical purposes that is made from cotton or synthetic fiber in the shape of a ball or a pad and that is used for applying medication to, or absorbing small amounts of body fluids from, a patient's body surface. Absorbent fibers intended solely for cosmetic purposes are not included in this generic device category.

Registrar Corp assists Medical Absorbent Fiber companies with:

  • FDA Medical Absorbent Fiber Establishment Registration
  • FDA Medical Absorbent Fiber Listing
  • FDA Medical Absorbent Fiber Label Requirements and Exceptions
  • FDA Medical Absorbent Fiber Import Information
  • FDA Medical Absorbent Fiber Detentions (Medical Absorbent Fiber Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Medical Absorbent Fiber Manufacturers (Medical Absorbent Fiber Suppliers)
       - Medical Absorbent Fiber Distributors
       - Medical Absorbent Fiber Processors
       - Medical Absorbent Fiber Repackers
       - Medical Absorbent Fiber Relabelers
       - Medical Absorbent Fiber Exporters
       - Medical Absorbent Fiber Importers
For more information about Medical Absorbent Fiber Medical Devices, simply click below:






 
U.S. FDA Regulations:

U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.


Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
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