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REACTIVO PARA LA DETERMINACIÓN DE FOSFATASA ALCALINA - COFEPRIS Registration 1208R2022 SSA

Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN DE FOSFATASA ALCALINA (REACTIVO PARA LA DETERMINACIÓN DE FOSFATASA ALCALINA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1208R2022 SSA and manufactured by LAB-CENTER DE MÉXICO S.A. DE C.V.. The device was registered on October 27, 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.

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COFEPRIS Official Data
Clase I
1208R2022 SSA
REACTIVO PARA LA DETERMINACIÓN DE FOSFATASA ALCALINA
COFEPRIS Analysis ID: 1208R2022 SSA
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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)
ALP-LQ
Trade Name (English)
ALP-LQ
Registration Information
Analysis ID
1208R2022 SSA
Registration Date
October 27, 2022
Manufacturer / Fabricante
Name (English)
LAB-CENTER DE MÉXICO S.A. DE C.V.