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With the UDI system (Unique Device Identification) manufacturers are obliged to identify and register medical devices. In the EU, the UDI is regulated within the framework of the MDR (Medical Device Regulation). In the USA, the FDA is authoritative. Seamless product tracking, less product piracy and highest patient safety are the goals. The challenges for manufacturers and marketers are no less demanding.
We bring you up to date on the current status of UDI direct marking of medical devices and give an overview of the UDI system according to MDR and FDA.
You will learn...
-why the UDI code is much more than a label and should not be underestimated
-what has to be considered for the technical implementation
-things to know about readability and code size
-how to achieve process reliability during direct marking
Fill out the form to the right to view the webinar recording and download the documents related to the webinar.
and get access to the webinar replay and the documents below.
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Lorem ipsum dolor sit amet, consetetur sadipscing elitr, sed diam nonumy eirmod tempor invidunt ut labore et dolore magna aliquyam erat, sed diam voluptua. At vero eos et accusam et justo duo dolores et ea rebum. Stet clita kasd gubergren, no sea takimata sanctus est Lorem ipsum dolor sit amet. Lorem ipsum dolor sit amet, consetetur sadipscing elitr, sed diam nonumy eirmod tempor invidunt ut labore et dolore magna aliquyam erat, sed diam voluptua. At vero eos et accusam et justo duo dolores et ea rebum. Stet clita kasd gubergren, no sea takimata sanctus est Lorem ipsum dolor sit amet.
Lorem ipsum dolor sit amet, consetetur sadipscing elitr, sed diam nonumy eirmod tempor invidunt ut labore et dolore magna aliquyam erat, sed diam voluptua. At vero eos et accusam et justo duo dolores et ea rebum. Stet clita kasd gubergren, no sea takimata sanctus est Lorem ipsum dolor sit amet.
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"Especially in the area of quality, FOBA fulfills our needs better than many other providers. In close cooperation with FOBA's laser marking experts, we set up the appropriate technical environment that allows us to comply with the high implementation requirements of UDI-marking on medical instruments. For us, the camera based marking validation being integrated in our production process is essential."
Nermin Duratovic, CEO - add'n solutions GmbH & Co. KG
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