PKLFOSFATASAALCALINADEALÍQUIDA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·AXMILAB, S.A. DE C.V.·Registered February 11, 2022PRUEBAPARALADETERMINACIÓNCUANTITATIVAINVITRODE FOSFATASA ALCALINA EN SUERO O PLASMA HUMANO.
TEST FOR THE QUANTITATIVE DETERMINATIONINVITRODE ALKALINE PHOSPHATASE IN HUMAN SERUM OR PLASMA.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA PARA DETERMINARFOSFATASA ALCALINA
- Trade Name (English)
- TEST TO DETERMINE ALKALINE PHOSPHATASE
- Analysis ID
- 100R2022 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 PKLFOSFATASAALCALINADEALÍQUIDA (PKLPHOSPHATAASEALKALINEALIQUID) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 100R2022 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. DIAGNOSTIC AGENTS), 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.