Registrar Corp

HomeMedical Devices510(k) Administrative ReviewMedical Device 510(k) Examples › U.S. FDA Human Dura Mater Regulations

U.S. FDA Medical Device Human Dura Mater Requirements: Human Dura Mater

FDA Medical Device Definition: Human dura mater is human pachymeninx tissue intended to repair defects in human dura mater

Registrar Corp assists Human Dura Mater companies with:

  • FDA Human Dura Mater Establishment Registration
  • FDA Human Dura Mater Listing
  • FDA Human Dura Mater Label Requirements and Exceptions
  • FDA Human Dura Mater Import Information
  • FDA Human Dura Mater Detentions (Human Dura Mater Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Human Dura Mater Manufacturers (Human Dura Mater Suppliers)
       - Human Dura Mater Distributors
       - Human Dura Mater Processors
       - Human Dura Mater Repackers
       - Human Dura Mater Relabelers
       - Human Dura Mater Exporters
       - Human Dura Mater Importers
For more information about Human Dura Mater Medical Devices, simply click below:

Live Help

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.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2016 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco