Mexico COFEPRIS registration 0023R2024 SSA

PRUEBA PARA LA DETECCIÓN DE LAS MUTACIONES V600 EN BRAF.

EN: PRUEBA PARA LA DETECCIÓN DE LAS MUTACIONES V600 EN BRAF.
Mexico flagMexico·Clase II·III. Agentes de diagnóstico·PRODUCTOS ROCHE, S.A. DE C.V.·Registered January 08, 2024
Device classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
COBAS® 4800 BRAF V600 MUTATION TEST ROCHE.
Trade Name (English)
COBAS® 4800 BRAF V600 MUTATION TEST ROCHE.
Registration information
Analysis ID
0023R2024 SSA
Registration Date
January 08, 2024
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DE C.V.
About this record

Access comprehensive regulatory information for PRUEBA PARA LA DETECCIÓN DE LAS MUTACIONES V600 EN BRAF. (PRUEBA PARA LA DETECCIÓN DE LAS MUTACIONES V600 EN BRAF.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0023R2024 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on January 08, 2024.

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.

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