Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Mycoplasma Detection Kit Regulations

U.S. FDA Medical Device Mycoplasma Detection Kit Requirements


FDA Medical Device Definition: Mycoplasma detection media and components are used to detect and isolate mycoplasma pleuropneumonia-like organisms (PPLO), a common microbial contaminant in cell cultures.

Registrar Corp assists Mycoplasma Detection Kit companies with:

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