PRUEBA PARA DETERMINAR FOSFATASA ALCALINA
Mexico·Clase I·III. Agentes de diagnóstico·AXMILAB, S.A. DE C.V.·Registered February 11, 2022- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- PKL FOSFATASA ALCALINA DEA LÍQUIDA
- Trade Name (English)
- PKL FOSFATASA ALCALINA DEA LÍQUIDA
- Analysis ID
- 0100R2022 SSA
- Registration Date
- February 11, 2022
- Name (Spanish)
- AXMILAB, S.A. DE C.V.
- Name (English)
- AXMILAB, S.A. DE C.V.
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 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.