Most establishments that are required to register with the FDA are also required to list the devices and the activities that are performed on those devices. Registrar Corp's team of Medical Device Regulatory Specialists provides guidance as to required elements, formats and particularities of medical device listings for US$ 195/device product code. Specifically, Registrar Corp:
Assists you in determining your device's likely classification
Prepares and submits your device listings to FDA and make changes, updates and cancellations as needed.
Issues Certificates of Registration to assure customers that you have a valid FDA Registration as well as prevent the accidental loss of your critical information.
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.
