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Filing a MAF for Antimicrobial Silver with the U.S. FDA

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


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

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

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

For more information about filing a MAF for Antimicrobial Silver, 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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