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U.S. FDA Medical Device Bed Board Requirements


FDA Medical Device Definition: A bed board is a device intended for medical purposes that consists of a stiff board used to increase the firmness of a bed.

Registrar Corp assists Bed Board companies with:

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