Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Non-Powered Breast Pump Regulations

U.S. FDA Medical Device Non-Powered Breast Pump Requirements


FDA Medical Device Definition: A nonpowered breast pump is a manual suction device used to express milk from the breast.

Registrar Corp assists Non-Powered Breast Pump companies with:

  • FDA Non-Powered Breast Pump Establishment Registration
  • FDA Non-Powered Breast Pump Listing
  • FDA Non-Powered Breast Pump Label Requirements and Exceptions
  • FDA Non-Powered Breast Pump Import Information
  • FDA Non-Powered Breast Pump Detentions (Non-Powered Breast Pump Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Non-Powered Breast Pump Manufacturers (Non-Powered Breast Pump Suppliers)
       - Non-Powered Breast Pump Distributors
       - Non-Powered Breast Pump Processors
       - Non-Powered Breast Pump Repackers
       - Non-Powered Breast Pump Relabelers
       - Non-Powered Breast Pump Exporters
       - Non-Powered Breast Pump Importers
For more information about Non-Powered Breast Pump 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 © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco