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U.S. FDA Medical Device Radiologic Patient Cradle Requirements


FDA Medical Device Definition: A radiologic patient cradle is a support device intended to be used for rotational positioning about the longitudinal axis of a patient during radiologic procedures.

Registrar Corp assists Radiologic Patient Cradle companies with:

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