In September of 2013 the Unique Device Identification (UDI) Ruling was put into action responding to the demand for more clarity, understanding and an easier way to update medical devices. Manufacturer’s have been implementing this ruling into their processes and come September 24, 2015 the second deadline will be put into action. Non-class III implantable, life-supporting or life-sustaining devices must be labeled with a UDI and devices that are multi-use must contain a permanent label.
Pragmatyxs has assisted in all cycles of UDI implementation, from label design and printing to reporting for updating the GUDID. Our expert team offers solution, implementation and life cycle support for your UDI project. Contact us with any questions or needs that you have .