by Innovit Corporate Affairs | Oct 16, 2019 | Blog, Eudamed
EUDAMED deadlines remain unchanged – the go-live date is still March 26, 2020 with the Date of Application for device registration/submission standing at May 26, 2020. Yet, we’re nearing the end of 2019 with most med device companies still struggling to fully...
by Innovit Corporate Affairs | Sep 19, 2019 | Blog, UDI
If you’re a medical device manufacturer or supplier submitting data to the FDA’s GUDID system, then your life may be getting a bit more complicated if you’re also using PTC’s UDI solution to comply with this FDA regulation. Recent announcements suggest that PTC is...
by Innovit Corporate Affairs | Jun 26, 2018 | News
Innovit, a global master data management solution provider, is releasing the Unique Device Identification (UDI) Multi-Connector solutions, helping medical device manufacturers keep pace with regulatory compliance standards....
by Innovit Corporate Affairs | Jun 11, 2018 | Blog, UDI
In 2013 the Food and Drug Administration issued a final rule setting out a system for Unique Device Identifiers, or UDIs, that should be applied to medical devices. These UDIs must be in both plain text and a format that can be read by a machine, such as a bar-code....