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

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


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

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

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

For more information about filing a MAF for Antimicrobial Compound, 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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