REAGENT KIT FOR CREATININE(CREA SOX) MINDRAY
Mexico·Clase I·III. DIAGNOSTIC AGENTS·MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.·Registered March 12, 2021PRUEBASINVITROPARALADETERMINACIÓNCUANTITATIVA DE LA CONCENTRACIÓN DECREATININA (CRE) EN SUERO, PLASMA UORINA EN SISTEMAS FOTOMÉTRICOS.AGENTEDEDIAGNÓSTICOPARAUSOINVITROPARA USO EXCLUSIVO EN LABORATORIOSCLÍNICOS O DE GABINETE
TESTSINVITROPARADEQUANTITATIVE DETERMINATION OF CREATININE CONCENTRATION (CRE) IN SERUM, PLASMA OR URINE IN PHOTOMETRIC SYSTEMS. DIAGNOSTIC AGENTFOR USEINVITROFOR USE IN CLINICAL OR CABINET LABORATORIES ONLY
- 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 DECREATININA MEDIANTE MÉTODO DESARCOSINA OXIDASA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF CREATININE BY METHOD DESARCOSINA OXIDASE
- Analysis ID
- 2053R2021 SSA
- Registration Date
- March 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 CREATININE(CREA SOX) MINDRAY (REAGENT KIT FOR CREATININE(CREA SOX) 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 2053R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on March 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.