REACTIVO PARA LA DETERMINACIÓN IN VITRO (IVD) DE ANTICUERPOS CONTRA VIRUS DE EPSTEIN-BARR (VCA GP 125, VCA P19, EBNA-1, P22 Y EA-D)TIROXINA
Mexico·Clase I·III. Agentes de diagnóstico·INOCHEM, S.A. DE
C.V.·Registered November 22, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- EUROLINE ANTI-EBV PROFILE 2 (IGM)
- Trade Name (English)
- EUROLINE ANTI-EBV PROFILE 2 (IGM)
- Analysis ID
- 1451R2022 SSA
- Registration Date
- November 22, 2022
- Name (Spanish)
- INOCHEM, S.A. DE C.V.
- Name (English)
- INOCHEM, S.A. DE C.V.
Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN IN VITRO (IVD) DE ANTICUERPOS CONTRA VIRUS DE EPSTEIN-BARR (VCA GP 125, VCA P19, EBNA-1, P22 Y EA-D)TIROXINA (REACTIVO PARA LA DETERMINACIÓN IN VITRO (IVD) DE ANTICUERPOS CONTRA VIRUS DE EPSTEIN-BARR (VCA GP 125, VCA P19, EBNA-1, P22 Y EA-D)TIROXINA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1451R2022 SSA and manufactured by INOCHEM, S.A. DE C.V.. The device was registered on November 22, 2022.
This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.