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U.S. FDA Medical Device Umbilical Occlusion Device Requirements


FDA Medical Device Definition: An umbilical occlusion device is a clip, tie, tape, or other article used to close the blood vessels in the umbilical cord of a newborn infant

Registrar Corp assists Umbilical Occlusion Device companies with:

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