OVERVIEW
Innovit’s UDI Connector products enable organizations responsible for UDI compliance to manage, validate, and submit product data to relevant regulatory databases through purpose-built connectors. Whether your organization requires compliance in a single market or across multiple jurisdictions, each connector provides standardized data management, built-in data validation, and machine-to-machine (M2M) submission capabilities aligned with the requirements of the relevant regulatory authority.
Use the datasheets below to explore the key capabilities, deployment options, and key benefits of each UDI Connector.
UDI Multi-Connector
Manage global UDI submissions through a single solution that supports multiple regulatory databases, including GUDID, EUDAMED, AusUDID, and swissdamed. Centralize device data, data validation, governance, and submissions while reducing operational complexity across global markets.
EUDAMED Connector
Manage European UDI submissions through a dedicated EUDAMED Connector that supports all EUDAMED data types, native data validation, M2M submission, and ongoing compliance with MDR and IVDR device registration requirements.
SWISSDAMED Connector
Support Swiss UDI compliance with a purpose-built connector designed for swissdamed device registration, enabling simplified data management, native data validation and streamlined submissions aligned with Swissmedic requirements.
GUDID Connector
Submit UDI data directly to the FDA’s Global Unique Device Identification Database (GUDID) using a purpose-built connector that simplifies data management, validation, submission, and ongoing compliance for the United States.
AUSUDID Connector
Simplify UDI compliance in Australia by managing, validating and submitting device information to the Therapeutic Goods Administration’s AusUDID through a dedicated, purpose-built connector that natively supports HL7 SPL submissions.
