Whitepaper: Meeting UDI Requirements

Find Out How Laser Marking Helps Ensure Your Devices Meet Requirements

In 2013, the FDA enacted a ruling requiring medical devices distributed in the U.S. to carry a unique device identifier – a UDI – to improve quality of information and tracking of the devices. UDIs are required to be present on the device if the device is intended for multiple uses and intended to be reprocessed before each use; in other words, non-disposable devices are required to have a UDI printed on them.

Free White Paper

If you manufacture these devices, it’s essential to comply with these requirements.

Download this informative white paper today, and learn how laser marking can help you meet UDI requirements.