START
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DE C.V.·Registered August 28, 2019REACTIVO PARA LA DETECCIÓN IN VITRO DEL EXCESO DE ANTÍGENO EN MUESTRAS HUMANAS UTILIZADO EN COMBINACIÓN CON EL REACTIVO DE LA PRUEBA INMUNOTURBIDIMÉTRICA CORRESPONDIENTE EN LOS SISTEMAS ROCHE. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO
REAGENT FOR IN VITRO DETECTION OF EXCESS ANTIGEN IN HUMAN SAMPLES USED IN COMBINATION WITH THE CORRESPONDING IMMUNOTURBIDIMETRIC TEST REAGENT IN ROCHE SYSTEMS. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR EXCLUSIVE 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 AUXILIAR PARA LA DETECCIÓN DE EXCESO DE ANTÍGENO EN MUESTRAS
- Trade Name (English)
- AUXILIARY REAGENT FOR THE DETECTION OF EXCESS ANTIGEN IN SAMPLES
- Analysis ID
- 1769R2019 SSA
- Registration Date
- August 28, 2019
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
Access comprehensive regulatory information for START (START) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1769R2019 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on August 28, 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.