Medical Device TIC Database is a SUNGO-associated information platform for checking medical device registrations, regulations, and testing standards across global markets. It brings together information from 14 official regulatory databases, including those of China, the European Union, the United States, the United Kingdom, Canada, and Australia, with company names verified against source records. Users can search registration records by company, product, or certificate number, and consult regulatory guidance, FDA product codes, recent 510(k) clearances, testing-standard listings, version status, and relevant testing organizations.

Free accounts can filter and export a limited number of results, while the platform also provides direct links to official sources. It offers a practical resource for manufacturers assessing overseas market access and buyers verifying suppliers. The broader SUNGO group provides medical device regulatory consulting, registration, local representation, testing, and quality-system certification services.

Its SUNGO LAB laboratories conduct safety, electromagnetic compatibility, packaging, sterilization, shelf-life, and performance testing. The database supplies references and official access links; it does not provide copyrighted standards or regulatory texts