UDI Multi-Connector datasheet

by ytatheer | April 30th, 2019 | Company Datasheets

Unique Device Identification (UDI) is a system first instituted by the FDA to mark and identify medical devices within the healthcare supply chain. It was implemented to help improve patient safety by solving traceability challenges such as product recalls and counterfeit devices. This regulation grouped devices into three risk classifications (Class III, Class II, Class I) and required medical device manufacturers to submit UDI information about their products to the GUDID (Global Unique Device Identification Database) – a central repository of device information intended for public access by healthcare providers and clinicians.

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