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U.S. FDA Medical Device Microsedimentation Centrifuge Requirements


FDA Medical Device Definition: A microsedimentation centrifuge is a device used to sediment red cells for the microsedimentation rate test.

Registrar Corp assists Microsedimentation Centrifuge companies with:

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