Tetraflex HD - EUDAMED Registration 00844369030212
Access comprehensive regulatory information for Tetraflex HD in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 00844369030212 and manufactured by Lenstec (Barbados) Inc. in Barbados.
This page provides complete registration details including trade name (Tetraflexโข HD), manufacturer information, authorized representative details, competent authority (ล tรกtny รบstav pre kontrolu lieฤiv / State Institute for Drug Control ( Slovak CA)), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.
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