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PRUEBA PARA DETERMINAR FOSFATASA ALCALINA - COFEPRIS Registration 0100R2022 SSA

Access comprehensive regulatory information for PRUEBA PARA DETERMINAR FOSFATASA ALCALINA (PRUEBA PARA DETERMINAR 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 0100R2022 SSA and manufactured by AXMILAB, S.A. DE C.V.. The device was registered on February 11, 2022.

This page provides complete registration details including product type (III. Agentes de diagn贸stico), 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
0100R2022 SSA
PRUEBA PARA DETERMINAR FOSFATASA ALCALINA
COFEPRIS Analysis ID: 0100R2022 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagn贸stico
Product Type (English)
III. Agentes de diagn贸stico
Trade Name (Spanish)
PKL FOSFATASA ALCALINA DEA L脥QUIDA
Trade Name (English)
PKL FOSFATASA ALCALINA DEA L脥QUIDA
Registration Information
Analysis ID
0100R2022 SSA
Registration Date
February 11, 2022
Manufacturer / Fabricante
Name (Spanish)
AXMILAB, S.A. DE C.V.
Name (English)
AXMILAB, S.A. DE C.V.