REAGENT KIT FOR GAMMA-GLUTAMIL TRANSFERASA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.·Registered February 12, 2021EL REACTIVO GGT ESTÁINDICADO PARALADETERMINACIÓN CUANTITATIVA DE LAACTIVIDAD DE GAMMA GLUTAMILTRANSFERSAENSUEROOPLASMAHUMANOEN SISTEMAS FOTOMÉTRICOS. AGENTE DEDIAGNÓSTICO PARA USO IN VITRO. PARA USO
THE GGT REAGENT IS INDICATED FOR THE QUANTITATIVE DETERMINATION OF THE ACTIVITY OF GAMMA GLUTAMYLTRANSFERSA IN HUMAN SERUM OR PLASMA IN PHOTOMETRIC SYSTEMS. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR USE
- 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 DEGAMMA GLUTAMIL TRANSFERASA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OFGAMMA GLUTAMYL TRANSFERASE
- Analysis ID
- 2038R2021 SSA
- Registration Date
- February 12, 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 GAMMA-GLUTAMIL TRANSFERASA (REAGENT KIT FOR GAMMA-GLUTAMIL TRANSFERASA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2038R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on February 12, 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.