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U.S. FDA Medical Device Snake-Bite Suction Kit Requirements


FDA Medical Device Definition: A suction snakebite kit is a device consisting of a knife, suction device, and tourniquet used for first-aid treatment of snakebites by removing venom from the wound.

Registrar Corp assists Snake-Bite Suction Kit companies with:

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