IMMUNOGLOBULIN M (IGM) DETECTION KIT (NEPHELOMETRY)
Mexico·Clase I·III. DIAGNOSTIC AGENTS·ATYDE MÉXICO S.A. DE C.V.·Registered December 02, 2019KIT PARA DETERMINACIÓN CUANTITATIVA IN VITRO DEL CONTENIDO DE IGM EN SUERO HUMANO O PLASMA. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES.
KIT FOR QUANTITATIVE IN VITRO DETERMINATION OF IGM CONTENT IN HUMAN SERUM OR PLASMA. 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 INMUNOGLOBULINA M (IGM).
- Trade Name (English)
- KIT OF REAGENTS FOR THE DETERMINATION OF IMMUNOGLOBULIN M (IGM).
- Analysis ID
- 2200R2019 SSA
- Registration Date
- December 02, 2019
- Name (Spanish)
- ATYDE MÉXICO S.A. DE C.V.
- Name (English)
- ATYDE MEXICO S.A. DE C.V.
Access comprehensive regulatory information for IMMUNOGLOBULIN M (IGM) DETECTION KIT (NEPHELOMETRY) (IMMUNOGLOBULIN M (IGM) DETECTION KIT (NEPHELOMETRY)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2200R2019 SSA and manufactured by ATYDE MÉXICO S.A. DE C.V.. The device was registered on December 02, 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.