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Filing a MAF for Artho-Phthalaldehyde with the U.S. FDA

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


Registrar Corp can help you to properly prepare and submit your Artho-Phthalaldehyde MAF to FDA.

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

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

For more information about filing a MAF for Artho-Phthalaldehyde, 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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