REAGENT KIT FOR ASPARTATEAMINOTRANSFERASEAST(AST/GOT)MINDRAY
Mexico·Clase I·III. DIAGNOSTIC AGENTS·MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.·Registered December 13, 2021EL REACTIVO AST ESTÁ INDICADO PARA LADETERMINACIÓN CUANTITATIVA DE LAACTIVIDADDEASTENSUEROOPLASMAENSISTEMAS FOTOMÉTRICOS. AGENTE DEDIAGNÓSTICOPARAUSOINVITRO. PARAUSOEXCLUSIVO EN LABORATORIOS CLÍNICOS ODE GABINETE
THE AST REAGENT IS INDICATED FOR THE QUANTITATIVE DETERMINATION OF THE ACTIVITY OF ASTENSUEROOPLASMA IN PHOTOMETRIC SYSTEMS. DIAGNOSTIC AGENTFORUSEINVITRO. FOR EXCLUSIVE USE IN CLINICAL LABORATORIES OR CABINET
- 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 DETERMINACIÓN DEASPARTATO AMINOTRANSFERASA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OFASPARTATE AMINOTRANSFERASE
- Analysis ID
- 2108R2021 SSA
- Registration Date
- December 13, 2021
- Name (Spanish)
- MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.
- Name (English)
- MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.
Access comprehensive regulatory information for REAGENT KIT FOR ASPARTATEAMINOTRANSFERASEAST(AST/GOT)MINDRAY (REAGENT KIT FOR ASPARTATEAMINOTRANSFERASEAST(AST/GOT)MINDRAY) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2108R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on December 13, 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.