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U.S. FDA Medical Device TLC Light U.V. Requirements

FDA Medical Device Definition: A thin-layer chromatography (TLC) system for clinical use is a device intended to separate one or more drugs or compounds from a mixture. The mixture of compounds is absorbed onto a stationary phase or thin layer of inert material (e.g., cellulose, alumina, etc.) and eluted off by a moving solvent (moving phase) until equilibrium occurs between the two phases.

Registrar Corp assists TLC Light U.V. companies with:

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