The GUDID (FDA) registration for medical devices of classes II and III has been mandatory for several years now, but the deadline is now getting closer for class I medical devices and unclassified medical devices.
The deadline is September 24, 2022.
What does this mean for you?
UDI compliance becomes mandatory for all devices!
Class I medical devices are those devices that have a low or moderate risk for the patient. Almost 47% of all medical devices fall into this category*.
You need a solution? You probably either already have or are planning to invest resources in registering your medical devices. With our GUDID attribute analysis and test service, we can quickly point you to the right areas of focus to ensure GUDID compliance and ensure compliant, fast and easy registration with our UDI solution - regardless whether for class I, II or III medical devices. Learn more
Register for a free consultation with one of our GUDID experts and let’s tackle your registration challenge together!
