With this certification, Hengst Filtration is laying a further foundation for the disproportionate expansion of its medical technology business in the coming years. In addition to cleanroom production at the headquarters in Münster, the Filtration Tech Center is currently being built. According to the company, new filtration solutions will be developed there in the future.
DIN EN ISO 13485 describes quality management for various stages in the life cycle of medical devices, including their installation, servicing and maintenance. "DIN EN ISO 13485 certification is the basis for a common language between manufacturers and suppliers. It defines uniform quality standards and processes," says Dr. Sebastian Stühle, Head of the Health Care Filtration Business Unit at Hengst.