CASETE DE PRUEBA RÁPIDA COMBINADA DE ROTAVIRUS Y ADENOVIRUS (HECES)
Mexico·Clase I·III. DIAGNOSTIC AGENTS·AMUNET, S.A. DE C.V.·Registered February 27, 2018EL CASETE DE PRUEBA RÁPIDA COMBINADA DE ROTAVIRUS Y ADENOVIRUS (HECES) ESTÁ INDICADO LA DETECCIÓN SIMULTÁNEA Y CUALITATIVA DE ROTAVIRUS Y ADENOVIRUS EN MUESTRAS DE HECES HUMANAS, LOS RESULTADOS DE LAS PRUEBAS PUEDEN SER ÚTILES PARA EL DIAGNÓSTICO DE INFEC
THE COMBINED ROTAVIRUS AND ADENOVIRUS (FECES) RAPID TEST CASSETTE IS INDICATED SIMULTANEOUS AND QUALITATIVE DETECTION OF ROTAVIRUS AND ADENOVIRUS IN HUMAN STOOL SAMPLES, TEST RESULTS MAY BE USEFUL FOR THE DIAGNOSIS OF INFECTIOUS
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA RÁPIDA COMBINADA DE ROTAVIRUS Y ADENOVIRUS
- Trade Name (English)
- COMBINED ROTAVIRUS AND ADENOVIRUS RAPID TEST
- Analysis ID
- 581R2018 SSA
- Registration Date
- February 27, 2018
- Name (Spanish)
- AMUNET, S.A. DE C.V.
- Name (English)
- AMUNET, S.A. DE C.V.
Access comprehensive regulatory information for CASETE DE PRUEBA RÁPIDA COMBINADA DE ROTAVIRUS Y ADENOVIRUS (HECES) (COMBINED ROTAVIRUS AND ADENOVIRUS (FECES) RAPID TEST CASSETTE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 581R2018 SSA and manufactured by AMUNET, S.A. DE C.V.. The device was registered on February 27, 2018.
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.