ANDROSTENEDIONE ELISA - COFEPRIS Registration 93R2019 SSA

Access comprehensive regulatory information for ANDROSTENEDIONE ELISA (ANDROSTENEDIONE ELISA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 93R2019 SSA and manufactured by INOCHEM SA DE CV. The device was registered on January 28, 2019.

This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.