Italy again extends deadline for registering products on medtech database
This article was originally published in RAJ Devices
Executive Summary
The Italian health ministry has for the second time extended the deadline – this time to 31 December 2009 – for medical device manufacturers to re-register their products onto the Repertorio database1. The re-registration is mandatory for all medical devices that were on the market when the new, controversial, registration requirements came into force in May 20072.
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