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U.S. FDA Medical Device Sahli Pipette Requirements

FDA Medical Device Definition: A manual blood cell counting device is a device used to count red blood cells, white blood cells, or blood platelets.

Registrar Corp assists Sahli Pipette companies with:

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