PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITATIVA DE ROTAVIRUS Y ADENOVIRUS EN HECES HUMANAS.
Mexico·Clase I·III. Agentes de
diagnóstico·CORPORINTER, S.A. DE C.V.·Registered July 01, 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)
- JUSCHEK® COMBO ROTAVIRUS AND ADENOVIRUS
- Trade Name (English)
- JUSCHEK® COMBO ROTAVIRUS AND ADENOVIRUS
- Analysis ID
- 1840R2024 SSA
- Registration Date
- July 01, 2024
- Name (Spanish)
- CORPORINTER, S.A. DE C.V.
- Name (English)
- CORPORINTER, S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITATIVA DE ROTAVIRUS Y ADENOVIRUS EN HECES HUMANAS. (PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITATIVA DE ROTAVIRUS Y ADENOVIRUS EN HECES HUMANAS.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1840R2024 SSA and manufactured by CORPORINTER, S.A. DE C.V.. The device was registered on July 01, 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.