KIT DE PRUEBA PARA LA DETERMINACIÓN IN VITRO (IVD) DE AUTOANTICUERPOS DE LA CLASE IGA CONTRA ENDOMISIO EN SUERO O PLASMA HUMANO
Mexico·Clase I·III. Agentes de
diagnóstico·INOCHEM, S.A. DE C.V.·Registered June 11, 2024- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- IIFT: COELIAC DISEASE SCREEN (EM) EUROPATTERN (IGA).
- Trade Name (English)
- IIFT: COELIAC DISEASE SCREEN (EM) EUROPATTERN (IGA).
- Analysis ID
- 1688R2024 SSA
- Registration Date
- June 11, 2024
- Name (Spanish)
- INOCHEM, S.A. DE C.V.
- Name (English)
- INOCHEM, S.A. DE C.V.
Access comprehensive regulatory information for KIT DE PRUEBA PARA LA DETERMINACIÓN IN VITRO (IVD) DE AUTOANTICUERPOS DE LA CLASE IGA CONTRA ENDOMISIO EN SUERO O PLASMA HUMANO (KIT DE PRUEBA PARA LA DETERMINACIÓN IN VITRO (IVD) DE AUTOANTICUERPOS DE LA CLASE IGA CONTRA ENDOMISIO EN SUERO O PLASMA HUMANO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1688R2024 SSA and manufactured by INOCHEM, S.A. DE C.V.. The device was registered on June 11, 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.