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U.S. FDA Medical Device Adhesive Tape Solvent Requirements


FDA Medical Device Definition: A surgical skin degreaser or an adhesive tape solvent is a device that consists of a liquid such as 1,1,2-trichloro-1,2,2-trifluoroethane; 1,1,1-trichloroethane; and 1,1,1-trichloroethane with mineral spirits intended to be used to dissolve surface skin oil or adhesive tape.

Registrar Corp assists Adhesive Tape Solvent companies with:

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