Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Papain Regulations

U.S. FDA Medical Device Papain Requirements

FDA Medical Device Definition: Enzyme preparations are products that are used in the histopathology laboratory for the following purposes:

Registrar Corp assists Papain companies with:

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

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 © 2017 Registrar Corp
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco