CARDIAC TROPONIN L (CTNL) TEST KIT (IMMUNOFLUORESCENCE).
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ATYDE MÉXICO S.A. DE C.V.·Registered November 26, 2019KIT PARA DETERMINACIÓN CUANTITATIVA IN VITRO DEL CONTENIDO DE CTNL EN SUERO HUMANO, PLASMA O SANGRE COMPLETA. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES
KIT FOR QUANTITATIVE IN VITRO DETERMINATION OF CTNL CONTENT IN HUMAN SERUM, PLASMA OR WHOLE BLOOD. 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)
- KIT DE REACTIVOS PARA LA DETERMINACIÓN DE TROPONINA CARDIACA L (CTNL).
- Trade Name (English)
- KIT OF REAGENTS FOR THE DETERMINATION OF CARDIAC TROPONIN L (CTNL).
- Analysis ID
- 2187R2019 SSA
- Registration Date
- November 26, 2019
- Name (Spanish)
- ATYDE MÉXICO S.A. DE C.V.
- Name (English)
- ATYDE MEXICO S.A. DE C.V.
Access comprehensive regulatory information for CARDIAC TROPONIN L (CTNL) TEST KIT (IMMUNOFLUORESCENCE). (CARDIAC TROPONIN L (CTNL) TEST KIT (IMMUNOFLUORESCENCE).) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2187R2019 SSA and manufactured by ATYDE MÉXICO 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.