TOXO IGG ELISA
Mexico·Clase I·III. DIAGNOSTIC AGENTS·INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.·Registered June 13, 2018EL TOXO IGG ELISA HA SIDO DISEÑADO PARA LA DETECCIÓN DE ANTICUERPOS DE CLASE INMUNOGLOBULINA G (IGG) HACIA TOXOPLASMA GONDII EN SUERO HUMANO. AGENTE DE DIAGNÓSTICO IN VITRO, PARA USO EXCLUSIVO DE LABORATORIO CLÍNICO O DE GABINETE.
THE TOXO IGG ELISA HAS BEEN DESIGNED FOR THE DETECTION OF IMMUNOGLOBULIN G (IGG) CLASS ANTIBODIES TO TOXOPLASMA GONDII IN HUMAN SERUM. IN VITRO DIAGNOSTIC AGENT, FOR CLINICAL LABORATORY OR CABINET USE ONLY.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ANÁLISIS ELISA PARA LA DETECCIÓN DE ANTICUERPOS IGG HACIA EL TOXOPLASMA GONDII
- Trade Name (English)
- ELISA ASSAY FOR THE DETECTION OF IGG ANTIBODIES TO TOXOPLASMA GONDII
- Analysis ID
- 1498R2018 SSA
- Registration Date
- June 13, 2018
- Name (Spanish)
- INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.
- Name (English)
- INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.
Access comprehensive regulatory information for TOXO IGG ELISA (TOXO IGG 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 1498R2018 SSA and manufactured by INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.. The device was registered on June 13, 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.