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Filing a MAF for Antioxidant Polyethylene with the U.S. FDA

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


Registrar Corp can help you to properly prepare and submit your Antioxidant Polyethylene MAF to FDA.

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

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

For more information about filing a MAF for Antioxidant Polyethylene, 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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