KLS Martin has implemented a total quality management system certified according to DIN EN ISO 13485, DIN EN ISO 9001 and the European legislation concerning medical devices. Of course, relevant national regulations have been taken into account as well - such as the requirements issued by the Food and Drug Administration (FDA) or the Canadian legislation.
This ensures that all our products are consistently checked in a controlled process until they are finally released after thorough testing and inspection (100% quality check). Rigorous quality control is supported by analyses and materials testing conducted in our own high-tech lab. And where necessary, we don't hesitate to have materials or products tested and approved by independent institutes before launching them on the market.