TRI-LEVEL CARDIAC CONTROL (CRD CONTROL)
Mexico·Clase I·III. DIAGNOSTIC AGENTS·SOLUCIÓN INTEGRAL A SUS NECESIDADES REGULATORIAS, S.A. DE C.V.·Registered August 07, 2018ESTE PRODUCTO ESTÁ DESTINADO PARA USO DIAGNÓSTICO IN VITRO, EN EL CONTROL DE CALIDAD DE MARCADORES CARDÍACOS EN QUÍMICA CLÍNICA Y SISTEMAS DE INMUNOENSAYO.
THIS PRODUCT IS INTENDED FOR IN VITRO DIAGNOSTIC USE, IN THE QUALITY CONTROL OF CARDIAC MARKERS IN CLINICAL CHEMISTRY AND IMMUNOASSAY 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 DE CONTROL
- Trade Name (English)
- CONTROL REAGENT
- Analysis ID
- 1947R2018 SSA
- Registration Date
- August 07, 2018
- Name (English)
- INTEGRAL SOLUTION TO YOUR REGULATORY NEEDS, S.A. DE C.V.
Access comprehensive regulatory information for TRI-LEVEL CARDIAC CONTROL (CRD CONTROL) (TRI-LEVEL CARDIAC CONTROL (CRD CONTROL)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1947R2018 SSA and manufactured by SOLUCIÓN INTEGRAL A SUS NECESIDADES REGULATORIAS, S.A. DE C.V.. The device was registered on August 07, 2018.
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.