ALINITY C ACTIVATED AMINOTRANFERASA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ABBOTT LABORATORIES DE MEXICO SA DE CV·Registered January 03, 2018SE UTILIZA PARA LA DETERMINACION CUANTITATIVA DE ALANINA AMINOTRANSFERASA EN SUERO O PLASMA HUMANOS EN EL ANALIZADOR ALINITY C
IT IS USED FOR THE QUANTITATIVE DETERMINATION OF ALANINE AMINOTRANSFERASE 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)
- REACTIVO PARA LA DETERMINACION DE ALANINA AMINOTRANSFERASA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF ALANINE AMINOTRANSFERASE
- Analysis ID
- 23R2018 SSA
- Registration Date
- January 03, 2018
- Name (Spanish)
- ABBOTT LABORATORIES DE MEXICO SA DE CV
- Name (English)
- ABBOTT LABORATORIES DE MEXICO SA DE CV
Access comprehensive regulatory information for ALINITY C ACTIVATED AMINOTRANFERASA (ALINITY C ACTIVATED AMINOTRANFERASA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 23R2018 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on January 03, 2018.
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.