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U.S. FDA Medical Device Tee (Water Trap) Drain Requirements


FDA Medical Device Definition: A tee drain (water trap) is a device intended to trap and drain water that collects in ventilator tubing during respiratory therapy, thereby preventing an increase in breathing resistance.

Registrar Corp assists Tee (Water Trap) Drain companies with:

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