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U.S. FDA Medical Device Umbilical Scissors Requirements

FDA Medical Device Definition: An obstetric-gynecologic general manual instrument is one of a group of devices used to perform simple obstetric and gynecologic manipulative functions. This generic type of device consists of the following Umbilical_Truss=A hernia support is a device, usually made of elastic, canvas, leather, or metal, that is intended to be placed over a hernial opening (a weakness in the abdominal wall) to prevent protrusion of the abdominal contents. This generic type of device includes the umbilical truss.

Registrar Corp assists Umbilical Scissors companies with:

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