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U.S. FDA Medical Device Unscented Menstrual Pad Requirements


FDA Medical Device Definition: Unscented_Menstrual_Pad=An unscented menstrual pad is a device that is a pad made of cellulosic or synthetic material which is used to absorb menstrual or other vaginal discharge. This generic type of device includes sterile unscented menstrual pads used for medically indicated conditions, but does not include menstrual pads treated with scent (i.e., fragrance materials) or those with added antimicrobial agents or other drugs.

Registrar Corp assists Unscented Menstrual Pad companies with:

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