PRUEBA RÁPIDA PARA LA DETERMINACIÓN CUALITATIVA DE INMUNOGLOBULINA E ESPECÍFICA (SIGE) DE ARTEMISA - COFEPRIS Registration 1305R2024 SSA

Access comprehensive regulatory information for PRUEBA RÁPIDA PARA LA DETERMINACIÓN CUALITATIVA DE INMUNOGLOBULINA E ESPECÍFICA (SIGE) DE ARTEMISA (PRUEBA RÁPIDA PARA LA DETERMINACIÓN CUALITATIVA DE INMUNOGLOBULINA E ESPECÍFICA (SIGE) DE ARTEMISA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1305R2024 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on May 07, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.