TÜV SÜD is a Notified Body providing services supporting CE marking and certification to ISO 13485, CMDCAS, and JPAL standards. TÜV SÜD assists medical device makers with global market access emphasizing Europe and North America. Services include auditing, expert clinical and biomedical engineering reviews, electrical, functional safety, EMC, and biocompatibility testing. TÜV SÜD participates in the Medical Device Single Audit Program. For more information on TÜV SÜD America’s Medical Health Services, please visit www.tuv-sud-america.com/medical or contact us at [email protected]
Our Product Service division TÜV is NRTL (Nationally Recognized Testing Laboratory) and SCC certified, providing a full suite of services, including CE Marking assistance, electromagnetic compatibility (EMC), electrical & mechanical testing, and many additional global conformity assessment services that help companies gain product compliance to enter individual country markets.