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U.S. FDA Medical Device Magnetic Locator Requirements

FDA Medical Device Definition: A permanent magnet is a nonelectric device that generates a magnetic field intended to find and remove metallic foreign bodies from eye tissue.

Registrar Corp assists Magnetic Locator companies with:

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