For more than three decades, TÜV SÜD's mission has revolved around ensuring the safety, quality, and sustainability of medical devices. As a premier Notified Body, we proudly hold accreditation from the IMDRF's Medical Device Single Audit Program (MDSAP), offering a route to demonstrate compliance with vital medical device standards across the United States, Canada, Japan, Brazil, and Australia. With more than 750 medical device experts in more than 30 locations worldwide, TÜV SÜD’s cutting-edge laboratories, professionals, international accreditations, and participation in the CB scheme facilitate market approval by providing robust testing reports and documentation, alongside medical device certification.