FDA Extends Compliance Date For GUDID For Some Devices After Discovering Security Flaw
In 2013, FDA introduced a new set of regulations that would establish a unique device identification system for medical devices. They also announced the dates for implementation, which would be done according to device classification. This set of regulations, called the Global Unique Device Identification Database (GUDID) would ensure compliance with the Agency’s required labeling and data submissions (full guidance here).
Earlier this month, FDA took the system offline after discovering a security vulnerability. Because of this, the Agency has announced that the compliance date for “non-class III implantable, life-supporting and life-sustaining medical devices” will be extended from September 24, 2015 to October 24, 2015 (see full guidance here).
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