PKL ALBÚMINA BCG.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·AXMILAB, S.A. DE C.V.·Registered March 10, 2022REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA INVITRODEALBÚMINAENSUEROOPLASMA. AGENTESDEDIAGNÓSTICO IN VITRO. PARA USO EXCLUSIVO DEEXCLUSIVO DE LABORATORIOS CLÍNICOS O DE GABINETE.
REAGENT FOR THE QUANTITATIVE DETERMINATION OF INVITRODEALALBUMIN IN SERUM OPLASMA. IN VITRO DIAGNOSTIC AGENTS. FOR THE EXCLUSIVE USE OF CLINICAL LABORATORIES OR CABINETS.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVOPARALAMEDICIÓNDE ALBÚMINA EN SUERO OPLASMA.
- Trade Name (English)
- REAGENT FOR ALBUMIN IN SERUM OR PLASMA.
- Analysis ID
- 180R2022 SSA
- Registration Date
- March 10, 2022
- Name (Spanish)
- AXMILAB, S.A. DE C.V.
- Name (English)
- AXMILAB, S.A. DE C.V.
Access comprehensive regulatory information for PKL ALBÚMINA BCG. (PKL ALBÚMINA BCG.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 180R2022 SSA and manufactured by AXMILAB, S.A. DE C.V.. The device was registered on March 10, 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.