Results 3 found
August 5th, 2015
MPO Summit

Linda Chatwin presenting at MPO Summit – “FDA Imperative – UDI” Click here for more information

March 12th, 2015
Unique Device Identification (UDI)

UL’S COMPLETE SERVICE OFFERING HELPS MANUFACTURERS ACHIEVE COMPLIANCE On September 24, 2013, the U.S. FDA published a final rule requiring medical devices to have a Unique Device Identifier. Applicable products must comply with the tiered implementation deadline, established by device classification.  This requirement extends to device manufacturers selling and marketing products in the U.S., including manufacturers… read more

March 26th, 2014
US FDA Unique Device Identification (UDI) implementation deadline in place for medical devices

On September 24, 2013, the U.S. FDA published the final rule requiring medical devices to have a Unique Device Identifier. Businesses must comply based on the tiered implementation deadline, established by device classification.  This requirement extends to all device manufacturers selling and marketing products in the U.S., including manufacturers exporting to the U.S.  The FDA compliance… read more