Mexico COFEPRIS registration 1100R2024 SSA

ANTICUERPO MONOCLONAL PARA LA DETECCIÓN INMUNOHISTOQUÍMICA CUALITATIVA DE CD5

EN: ANTICUERPO MONOCLONAL PARA LA DETECCIÓN INMUNOHISTOQUÍMICA CUALITATIVA DE CD5
Mexico flagMexico·Clase II·III. Agentes de diagnóstico·PRODUCTOS ROCHE, S.A. DE C.V.·Registered April 18, 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)
CONFIRM ANTI-CD5 (SP19) RABBIT MONOCLONAL PRIMARY ANTIBODY
Trade Name (English)
CONFIRM ANTI-CD5 (SP19) RABBIT MONOCLONAL PRIMARY ANTIBODY
Registration information
Analysis ID
1100R2024 SSA
Registration Date
April 18, 2024
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DE C.V.
About this record

Access comprehensive regulatory information for ANTICUERPO MONOCLONAL PARA LA DETECCIÓN INMUNOHISTOQUÍMICA CUALITATIVA DE CD5 (ANTICUERPO MONOCLONAL PARA LA DETECCIÓN INMUNOHISTOQUÍMICA CUALITATIVA DE CD5) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1100R2024 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on April 18, 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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