Mexico COFEPRIS registration 0917R2024 SSA

REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE ALBÚMINA

EN: REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE ALBÚMINA
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·BECKMAN COULTER DE MÉXICO, S.A. DE C.V.·Registered April 04, 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)
BECKMAN COULTER® ALBÚMINA
Trade Name (English)
BECKMAN COULTER® ALBÚMINA
Registration information
Analysis ID
0917R2024 SSA
Registration Date
April 04, 2024
Manufacturer / Fabricante
Name (English)
BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
About this record

Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE ALBÚMINA (REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE ALBÚMINA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0917R2024 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on April 04, 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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