Manufacturing for the Future Exposition in Hartford, CT. May 3 – 5, 2016 – Visit Us at Booth #1817 DOWNLOAD A COMPLIMENTARY GUEST PASS HERE! Just tell them you’re with ImageTek Labels (wink, wink). MFG4 for Aerospace, Industrial and Military Defense With today’s ever evolving manufacturing climate, technology is constantly adapting and changing… moving towards custom,
Are You Prepared for the FDA’s Medical Device Labeling Regulations? The Food & Drug Administration (FDA) has announced the final ruling that will require medical device manufacturers to label each unique medical device distributed in the U.S. with a UDI “Unique Device Identifier” label. Are you prepared for the FDA’s medical device labeling regulations? The
New UL/IEC 60601-1 3rd edition regulations have been extended until Dec 31st, 2013 New regulations proposed by the FDA are in the final stage rulings. The new legislation affects over 25,000 medical device manufacturers worldwide. Are you one of them? Beginning in 2014, manufacturers of most medical devices will be required to mark all manufactured
