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Filing a MAF for Acrylic with the U.S. FDA

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

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

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

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

For more information about filing a MAF for Acrylic, 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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