ALINITY C ACTIVATED ASPARTATEAMINOTRANSFERASE.
BELENZOEDNIASZAEYPOINES ASCETIVATED ASPARTATEAMINOTRANSFERASE SE UTILIZA PARA LADETERMINACIÓN CUANTITATIVA DEASPARTATOAMINOTRANSFERASA ENSUEROO PLASMA HUMANOS EN EL ALINITY CSYSTEM. AGENTE DE DIAGNÓSTICO PARAUSO IN VITRO. PARA USO EXCLUSIVO ENLABORATORIOS CLÍNICOS Y DE GABINETE.
BELENZOEDNIASZAEYPOINES ASCETIVATED ASPARTATEAMINOTRANSFERASE IS USED FOR THE QUANTITATIVE DETERMINATION OFASPARTATE AMINOTRANSFERASE IN HUMAN SERUM OR PLASMA IN THE ALINITY CSYSTEM. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR EXCLUSIVE USE IN CLINICAL AND CABINET LABORATORIES.
- 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 DETERMINACIÓNCUANTITATIVA DE ASPARTATOAMINOTRANSFERASA.
- Trade Name (English)
- ASSAY FOR THE QUANTITATIVE DETERMINATION OF ASPARTATE AMINOTRANSFERASE.
- Analysis ID
- 1851R2021 SSA
- Registration Date
- November 16, 2021
- Name (Spanish)
- ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for ALINITY C ACTIVATED ASPARTATEAMINOTRANSFERASE. (ALINITY C ACTIVATED ASPARTATEAMINOTRANSFERASE.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1851R2021 SSA and manufactured by ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on November 16, 2021.
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.