REAGENT KIT FOR URIC ACID (UA)MINDRAY
Mexico·Clase I·III. DIAGNOSTIC AGENTS·MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.·Registered February 12, 2021DPREUSEEEBNA SLIIGNAVRI TYR DOIVPIDARIRA VLAASODSE,T HEARCMEINS ADCEI ÓNCUANTITATIVADELACONCENTRACIÓNDEAUEN SUERO, PLASMA U ORINA EN SISTEMASFOTOMÉTRICOS.
DPREUSEEEBNA SLIIGNAVRI TYR DOIVPIDARIRA VLAASODSE,T HEARCMEINS QUANTITATIVE ASSESSMENT OF THE CONCENTRATION OF SERUM, PLASMA OR URINE IN PHOTOMETRIC SYSTEMS.
- 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 DEÁCIDOÚRICOMEDIANTEMÉTODOURICASAPEROXIDASA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OFACIDURIC BYMETHOD URICASAPEROXIDASA
- Analysis ID
- 2042R2021 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 URIC ACID (UA)MINDRAY (REAGENT KIT FOR URIC ACID (UA)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 2042R2021 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.