Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Carbon-Dioxide Absorbent Regulations

U.S. FDA Medical Device Carbon-Dioxide Absorbent Requirements


FDA Medical Device Definition: A carbon dioxide absorbent is a device intended for medical purposes that consists of an absorbent material (e.g., soda lime) that is intended to remove carbon dioxide from the gases in the breathing circuit.

Registrar Corp assists Carbon-Dioxide Absorbent companies with:

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