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Schedule a UDI Conference Call

The U.S. Food and Drug Administration (FDA) has new regulations requiring most medical devices distributed in the United States to bear a Unique Device Identifier (UDI). FDA also requires submission of device and UDI information to the Global Unique Device Identifier Database (GUDID).

The date by which you must comply with these new UDI requirements is based on the FDA Product Codes of your devices. Registrar Corp’s Regulatory Specialists are happy to discuss these new regulations in the context of your specific products and needs. Simply schedule a conference call using the form below.