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Filing a MAF for Auto Injector with the U.S. FDA

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

  - USA

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

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

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

For more information about filing a MAF for Auto Injector, 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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