Results 2 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