Registrar Corp

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

U.S. FDA Medical Device Infusion Stand Requirements


FDA Medical Device Definition: The infusion stand is a stationary or movable stand intended to hold infusion liquids, infusion accessories, and other medical devices.

Registrar Corp assists Infusion Stand companies with:

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