Tracking Surgical Instruments – Save Lives – Save Money

a tray with many surgical instruments lined up with the operating room in the background

Tracking Surgical Instruments: Releasing massive untapped value in the surgical instrument life cycle.

The EU Commission, meeting the FDA regulations established last year, has clearly defined the requirements for implementation of a Unique Device Identification (UDI) System in the final text of the new EU Medical Device Regulation (MDR) 2017/745 and the In Vitro Diagnostic Medical Device Regulation (IVDR) 2017/746, published at the beginning of May.

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