CONTROLES HEMATOLÓGICOS WRP CHECK
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PRODUCTOS ROCHE, S.A. DE C.V.·Registered November 26, 2019LOS CONTROLES HEMATOLÓGICOS SE EMPLEAN PARA LA VERIFICACIÓN DEL RANGO REPORTABLE EN LOS ANALIZADORES HEMATOLÓGICOS. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES
HAEMATOLOGICAL CHECKS ARE USED FOR VERIFICATION OF REPORTABLE RANGE ON HAEMATOLOGICAL ANALYSERS. 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)
- REACTIVOS CONTROL
- Trade Name (English)
- CONTROL REAGENTS
- Analysis ID
- 2188R2019 SSA
- Registration Date
- November 26, 2019
- Name (Spanish)
- PRODUCTOS ROCHE, S.A. DE C.V.
- Name (English)
- PRODUCTOS ROCHE, S.A. DE C.V.
Access comprehensive regulatory information for CONTROLES HEMATOLÓGICOS WRP CHECK (HAEMATOLOGICAL CONTROLS WRP CHECK) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2188R2019 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on November 26, 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.