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Filing a MAF for Askina Hydrocolloid Wound Dressings with the U.S. FDA


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

  - B. BRAUN/MCGAW

Registrar Corp can help you to properly prepare and submit your Askina Hydrocolloid Wound Dressings MAF to FDA.

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

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

For more information about filing a MAF for Askina Hydrocolloid Wound Dressings, 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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