Velleuer receives DIN EN ISO 13485 certification
We are delighted to announce that Velleuer GmbH & Co. KG has successfully been certified according to DIN EN ISO 13485.
With this internationally recognised standard for quality management systems in medical technology, we meet the high requirements for process reliability, risk management, documentation and continuous improvement. The certification marks an important milestone in our company’s development and lays the foundation for the further expansion of our activities in the field of medical technology.
Quality throughout the entire production process
DIN EN ISO 13485 confirms that all production steps, from goods receipt to manufacturing and delivery, are fully monitored, documented and validated. This enables us to meet the most stringent regulatory requirements and strengthen our position as a reliable partner for medical components.
Horst Schillians, Managing Director of Velleuer GmbH & Co. KG, emphasises the strategic importance of this success:
“Certification according to DIN EN ISO 13485 is an important strategic step for us. It confirms the high quality of our manufacturing processes and builds trust among our customers in the medical technology sector. At the same time, it demonstrates the great commitment of our entire team, which has worked intensively over the past few months to implement the requirements.”
As part of the Lesjöfors Group, we also benefit from the group-wide understanding of quality and the professional exchange within the international network.
We would like to thank our entire team for their tremendous efforts and look forward to further expanding our expertise in the field of medical components.
