FAQ: Global Unique Device Identification Database (GUDID)

FAQ: Global Unique Device Identification Database (GUDID)

What is GUDID? GUDID is an acronym for the Global Unique Device Identification Database — a central repository of detailed medical device information created by the US FDA.  It is often pronounced “Good ID”.  The GUDID system was implemented as a component of the...
Introducing Innovit’s EUDAMED Reference Center

Introducing Innovit’s EUDAMED Reference Center

As a medical device provider one of the biggest changes on the horizon will be the new EU requirements for product information, as well as the FDA’s GUDID compliance deadline for Class I medical devices.   Even the most experienced companies uncover critical gaps in...
Innovit’s 2021 Recap and a Look Ahead!

Innovit’s 2021 Recap and a Look Ahead!

2022 is almost here and the holiday season is in full flight!   As another turbulent year comes to an end, the team at Innovit took a moment to reflect on the past year while also looking ahead with zeal and optimism. Though agility and adaptability are nothing new...

Introducing Innovit’s EUDAMED Reference Center

As a medical device provider one of the biggest changes on the horizon will be the new EU requirements for product information, as well as the FDA’s GUDID compliance deadline for Class I medical devices.   Even the most experienced companies uncover critical gaps in...