Mexico COFEPRIS registration 1312R2024 SSA

KIT DE REACTIVOS Y CALIBRADORES

EN: KIT DE REACTIVOS Y CALIBRADORES
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·BECKMAN COULTER DE MÉXICO, S.A. DE C.V.·Registered May 07, 2024
Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
TOTAL IMMUNOGLOBULIN E (IGE) REF. C22529
Trade Name (English)
TOTAL IMMUNOGLOBULIN E (IGE) REF. C22529
Registration information
Analysis ID
1312R2024 SSA
Registration Date
May 07, 2024
Manufacturer / Fabricante
Name (English)
BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
About this record

Access comprehensive regulatory information for KIT DE REACTIVOS Y CALIBRADORES (KIT DE REACTIVOS Y CALIBRADORES) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1312R2024 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on May 07, 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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