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U.S. FDA Medical Device Deodorized Menstrual Pad Requirements: Deodorized Menstrual Pad

FDA Medical Device Definition: A scented or scented deodorized 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. It has scent (i.e., fragrance materials) added for aesthetic purposes (scented menstrual pad) or for deodorizing purposes (scented deodorized menstrual pad). This generic type of device includes sterile scented menstrual pads used for medically indicated conditions, but does not include menstrual pads treated with added antimicrobial agents or other drugs

Registrar Corp assists Deodorized Menstrual Pad companies with:

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




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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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