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

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


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

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

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

For more information about filing a MAF for Adhesives, 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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