ALINITY C A-1-AGP
ALINITY C A-1-AGP REAGENT KIT EL ENSAYO ALINITY C A-1-AGP SE UTILIZA PARA LA DETERMINACIÓN CUANTITATIVA DE ALFA-1 GLUCOPROTEÍNA ÁCIDA EN SUERO O PLASMA HUMANOS EN EL ANALIZADOR ALINITY C.
ALINITY C A-1-AGP REAGENT KIT THE ALINITY C A-1-AGP ASSAY IS USED FOR THE QUANTITATIVE DETERMINATION OF ALPHA-1 ACID GLYCOPROTEIN IN HUMAN SERUM OR PLASMA IN THE ALINITY C ANALYZER.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO PARA LA DETERMINACIÓN DE ALFA-1 GLUCOPROTEÍNA ÁCIDA.
- Trade Name (English)
- ASSAY FOR THE DETERMINATION OF ALPHA-1 ACID GLYCOPROTEIN.
- Analysis ID
- 1593R2019 SSA
- Registration Date
- August 12, 2019
- Name (Spanish)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for ALINITY C A-1-AGP (ALINITY C A-1-AGP) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1593R2019 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on August 12, 2019.
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.