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High quality standards for medical products
Our quality management system is DIN EN ISO 13485:2007 certified for medical products. Since the mid-nineties, additional quality management standards have been set. These standards more precisely define the requirements of ISO 9001 in order to ensure that the necessary standards for developing and manufacturing medical products are met.

Risk management plays a central role in identifying potential problems that can arise from medical products or their use. Risks can be reduced or eliminated during the development process and in later product life cycles.
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ISO 13485:2007