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Reprocessing of laser-marked medical devices with process reliability

Whitepaper on best practices, labeling concepts and verifiable cleaning processes

Laser-marked instruments have to withstand multiple cleaning and sterilisation cycles without any loss of information – while at the same time ensuring a safe, economical process. The whitepaper shows you how to coordinate labeling, materials and preparation in such a way that UDI and traceability requirements are reliably met. Benefit from practical advice for manufacturers, processing companies and clinics.

  • Requirements for legibility, contrast and durability of laser markings after typical cleaning and sterilisation processes
  • Influence of material, surface roughness and marking parameters on corrosion behavior and biocompatibility
  • Design of robust UDI and Data Matrix Codes for automated identification and traceability
  • Validation and routine control of reprocessing processes procedures to ensure long-term stability of markings
  • Practical examples of the integration of laser marking into existing production and processing chains
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Reprocessing of laser-marked medical products
According to MDR and FDA regulations, labels on medical devices must be clear and legible throughout the life cycle. This study presents results on the reprocessing of laser-marked medical steel 1.4301. Find out more in this white paper.