PRUEBA RÁPIDA EN CASETE DEL ANTÍGENO DE LA SALMONELLA TYPHI EN HECES
Mexico·Clase I·III. Agentes de
diagnóstico·QUIMIBIOL, S.A. DE C.V.·Registered April 18, 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)
- MEXLAB BIO- SALMONELLA TYPHI
- Trade Name (English)
- MEXLAB BIO- SALMONELLA TYPHI
- Analysis ID
- 1102R2024 SSA
- Registration Date
- April 18, 2024
- Name (Spanish)
- QUIMIBIOL, S.A. DE C.V.
- Name (English)
- QUIMIBIOL, S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA RÁPIDA EN CASETE DEL ANTÍGENO DE LA SALMONELLA TYPHI EN HECES (PRUEBA RÁPIDA EN CASETE DEL ANTÍGENO DE LA SALMONELLA TYPHI EN HECES) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1102R2024 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on April 18, 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.