This conversion is integrated into the label harmonization project within the KLS Martin Group and at the same time we have taken advantage of realizing the FDA's UDI requirements to benefit from possible synergies. As soon as the new Medical Device Directive for Europe becomes effective, this will also require the introduction of a UDI labelling system in terms of traceability. This joint standard will increase patient safety as well as giving leverage to possible rationalization potential across the entire supply chain.
Please note that products in stock already labeled may temporarily still be marked with the old code.
We will support you in the conversion to the GS1 standard, please contact us:
Tel: +49 7461 706-0
You can find information on the GS1 standard directly on the homepage of the GS1 organization: