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U.S. FDA Medical Device Patient Lift Requirements


FDA Medical Device Definition: An AC-powered lift is an electrically powered device either fixed or mobile, used to lift and transport patients in the horizontal or other required position from one place to another, as from a bed to a bath. The device includes straps and slings to support the patient.

Registrar Corp assists Patient Lift companies with:

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