PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITTATIVA DE ANTÍGENO DE ADENOVIRUS, ANTÍGENO DEL VIRUS SINCITIAL RESPIRATORIO Y ANTIGENOS DE INFLUENZA A Y B
Mexico·Clase I·III. Agentes de
diagnóstico·KABLA COMERCIAL, S.A.
DE C.V.·Registered July 04, 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)
- CERTUM ADENOVIRUS/RSV/INFLUE NZA A+B COMBO RAPID TEST CASSETTE (NASOPHARYNGEAL SWAB)
- Trade Name (English)
- CERTUM ADENOVIRUS/RSV/INFLUE NZA A+B COMBO RAPID TEST CASSETTE (NASOPHARYNGEAL SWAB)
- Analysis ID
- 1883R2024 SSA
- Registration Date
- July 04, 2024
- Name (Spanish)
- KABLA COMERCIAL, S.A. DE C.V.
- Name (English)
- KABLA COMERCIAL, S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITTATIVA DE ANTÍGENO DE ADENOVIRUS, ANTÍGENO DEL VIRUS SINCITIAL RESPIRATORIO Y ANTIGENOS DE INFLUENZA A Y B (PRUEBA RÁPIDA PARA LA DETECCIÓN CUALITTATIVA DE ANTÍGENO DE ADENOVIRUS, ANTÍGENO DEL VIRUS SINCITIAL RESPIRATORIO Y ANTIGENOS DE INFLUENZA A Y B) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1883R2024 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on July 04, 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.