TRSF2 ROCHE
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DE C.V.·Registered November 05, 2019PARA LA DETERMINACIÓN CUANTITATIVA DE TRANSFERRINA EN ORINA, SUERO Y PLASMA HUMANOS EN LOS ANALIZADORES DE QUÍMICA CLÍNICA ROCHE. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES.
FOR THE QUANTITATIVE DETERMINATION OF TRANSFERRIN IN HUMAN URINE, SERUM AND PLASMA IN ROCHE CLINICAL CHEMISTRY ANALYZERS. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR 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)
- PRUEBA PARA LA DETERMINACIÓN DE TRANSFERRINA.
- Trade Name (English)
- TEST FOR THE DETERMINATION OF TRANSFERRIN.
- Analysis ID
- 2084R2019 SSA
- Registration Date
- November 05, 2019
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
Access comprehensive regulatory information for TRSF2 ROCHE (TRSF2 ROCHE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2084R2019 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on November 05, 2019.
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.