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Webinar recording
Laser marking on metals like titanium or stainless steel can cause corrosion in the lasered areas. But only if corrosion is prevented, the direct mark on a medical device will remain durable throughout its lifetime. In addition, particle emission can only be prevented if the surface is intact, so that biocompatibility can be guaranteed, e.g. of an implant.
Therefore, direct marking of medical devices should be understood as a multi-stage process that is not completed with laser marking alone. Rather, pretreatment, passivation and cleaning are among the surface treatment steps that are necessary to prevent corrosion. In order to ensure all the normative aspects, a process validation should also be performed to achieve UDI-compliant code marking.
Some of the questions that will be addressed in the Expert Talk are:
- What surface treatment is legally required by MDR/FDA for UDI labeling?
- How do the different steps of the marking process steps correlate?
- What needs to be considered for a comprehensive validation of the surface treatment process?
- How do the material properties and the marking technology impact the marking results?
You didn't find the time to attend the webinar? Or you did join but want to review the recording?
No problem, just fill in the form to get access to the webinar replay immediately.
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.
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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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