ASCA-IGG/IGA
Mexico·Clase II·III. DIAGNOSTIC AGENTS·BIO SIMEX, S.A. DE C.V.·Registered May 31, 2019REACTIVOS PARA LA DETERMINACIÓN CUALITATIVA Y CUANTITATIVA DE ASCA-IGG/IGA EN SUERO O PLASMA HUMANOS.
REAGENTS FOR THE QUALITATIVE AND QUANTITATIVE DETERMINATION OF ASCA-IGG/IGA IN HUMAN SERUM OR PLASMA.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVO PARA LA DETERMINACIÓN DE ASCA-IGG/IGA
- Trade Name (English)
- REAGENT FOR THE DETERMINATION OF ASCA-IGG/IGA
- Analysis ID
- 1194R2019 SSA
- Registration Date
- May 31, 2019
- Name (Spanish)
- BIO SIMEX, S.A. DE C.V.
- Name (English)
- BIO SIMEX, S.A. DE C.V.
Access comprehensive regulatory information for ASCA-IGG/IGA (ASCA-IGG/IGA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1194R2019 SSA and manufactured by BIO SIMEX, S.A. DE C.V.. The device was registered on May 31, 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.