Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Blood-Bank Centrifuge Regulations

U.S. FDA Medical Device Blood-Bank Centrifuge Requirements


FDA Medical Device Definition: A blood bank centrifuge for in vitro diagnostic use is a device used only to separate blood cells for further diagnostic testing.

Registrar Corp assists Blood-Bank Centrifuge companies with:

  • FDA Blood-Bank Centrifuge Establishment Registration
  • FDA Blood-Bank Centrifuge Listing
  • FDA Blood-Bank Centrifuge Label Requirements and Exceptions
  • FDA Blood-Bank Centrifuge Import Information
  • FDA Blood-Bank Centrifuge Detentions (Blood-Bank Centrifuge Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Blood-Bank Centrifuge Manufacturers (Blood-Bank Centrifuge Suppliers)
       - Blood-Bank Centrifuge Distributors
       - Blood-Bank Centrifuge Processors
       - Blood-Bank Centrifuge Repackers
       - Blood-Bank Centrifuge Relabelers
       - Blood-Bank Centrifuge Exporters
       - Blood-Bank Centrifuge Importers
For more information about Blood-Bank 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.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco