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U.S. FDA Medical Device Medical Devices Disinfectant Requirements


FDA Medical Device Definition: A general purpose disinfectant is a germicide intended to process noncritical medical devices and equipment surfaces. A general purpose disinfectant can be used to preclean or decontaminate critical or semicritical medical devices prior to terminal sterilization or high level disinfection. Noncritical medical devices make only topical contact with intact skin.

Registrar Corp assists Medical Devices Disinfectant companies with:

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