TUV SUD Product Service

TUV SUD Product Service GmbH was authorized by the EU in June 2020, and is one of the few notified bodies with both the new IVDR regulations and the previous IVDD qualifications. Medical devices must be certified before being placed on the market. As the largest notified body for medical devices and in vitro diagnostic medical devices, TUV SUD has over 30 years of experience in providing certification services to manufacturers and suppliers. TUV SUD has more than 130 authorized IVD experts dedicated to offering safe, reliable, high-quality, and sustainable services at all stages from product design, development, testing, certification, to final approval. The success of TUV SUD's certification business is due to the joint efforts of experts from different countries and regions who are familiar with local regulations.