FERRITIN ELISA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·DIAGMEX, S.A. DE C.V.·Registered August 01, 2019KIT DE PRUEBA DESTINADA A LA DETERMINACIÓN CUANTITATIVA DE LA CONCENTRACIÓN DE FERRITINA HUMANA. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES
TEST KIT FOR THE QUANTITATIVE DETERMINATION OF HUMAN FERRITIN CONCENTRATION. 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 PARA LA DETERMINACIÓN DE FERRITINA HUMANA.
- Trade Name (English)
- REAGENTS FOR THE DETERMINATION OF HUMAN FERRITIN.
- Analysis ID
- 1525R2019 SSA
- Registration Date
- August 01, 2019
- Name (Spanish)
- DIAGMEX, S.A. DE C.V.
- Name (English)
- DIAGMEX, S.A. DE C.V.
Access comprehensive regulatory information for FERRITIN ELISA (FERRITIN ELISA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1525R2019 SSA and manufactured by DIAGMEX, S.A. DE C.V.. The device was registered on August 01, 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.