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Filing a MAF for Applied Liquid Silicone Rubber with the U.S. FDA


Filing a medical device master file (MAF) for Applied Liquid Silicone Rubber can be a useful mechanism to market your Applied Liquid Silicone Rubber to the U.S. Medical Device Industry. Typical Applied Liquid Silicone Rubber producers who have filed a MAF for Applied Liquid Silicone Rubber include:

  - RHODIA INC.

Registrar Corp can help you to properly prepare and submit your Applied Liquid Silicone Rubber MAF to FDA.

As your Agent, Registrar Corp will perform the following administrative functions:

  - Ensure administrative accuracy of your Applied Liquid Silicone Rubber MAF
  - Format, assemble and deliver your Applied Liquid Silicone Rubber MAF to FDA
  - Assist with preparing letters of authorization regarding your Applied Liquid Silicone Rubber MAF
 - Provide changes, additions and maintenance of your Applied Liquid Silicone Rubber MAF
  - Respond to issues relating to ownership of your Applied Liquid Silicone Rubber MAF
  - Assist with submission of responses to FDA concerning your Applied Liquid Silicone Rubber MAF

For more information about filing a MAF for Applied Liquid Silicone Rubber, simply click below:




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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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