Unique Device Identification

What does UDI stand for?

The Unique Device Identification (UDI) is a system set up by the FDA for identifying medical devices. The objective is patient safety. Since September 2014, products which are supplied to the USA must be successively (depending on their product classification) marked with a barcode. It is to be expected that Canada, Europe and Asia will stipulate similar requirements in the future.

We have set up the UDI system for our own Cendres+Métaux products. We would be pleased to pass on the valuable experiences gained. Our specialists can advice you on an individual basis with regard to the concept of the code, through master data management up to printing the code on the packaging. Do you intend to organise UDI control (GTIN No.) via SAP? We can also offer you extensive support here. A major advantage for you: the appropriate labels are designed and printed ready-to-use by us.