Create a search profile
The agent extracts the generic product identity, intended function, technology, and risk-driving features.

Describe a product and search the TMDA registration database for similar medical devices, with AI-ranked matches and direct record links.
Turn the intended use and technology into concise generic device identities.
Run English and local-language searches against the selected registration records.
Compare intended function and technical fit, with clear limitations for every match.
Include intended use, users, patient population, operating principle, contact duration, and whether the device is sterile, measuring, active, implantable, software, or an IVD.
The agent extracts the generic product identity, intended function, technology, and risk-driving features.
Each selected registry gets concise English and local-language searches against its actual registration records.
The agent ranks only retrieved records and explains whether each is a strong, possible, or broad reference.
It searches the selected countriesโ medical device registration databases using generic English and local-language product terms generated from your description.
No. A database match is a research lead, not proof of equivalence, classification, or eligibility for a pathway. Intended use and technological differences must be reviewed.
Each regulator publishes different fields and coverage, product names vary by language, and some databases include risk class while others expose only product or registration details.
Describe the generic product type, intended purpose, user, patient population, operating principle, contact duration, sterility, software role, and major risk-driving characteristics.