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Filing a MAF for Acrylonitrite Butadiene Styrene with the U.S. FDA


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

  - B. BRAUN/MCGAW

Registrar Corp can help you to properly prepare and submit your Acrylonitrite Butadiene Styrene MAF to FDA.

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

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

For more information about filing a MAF for Acrylonitrite Butadiene Styrene, 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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