TOXO IGG ELISA - COFEPRIS Registration 1498R2018 SSA
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.
EL 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.