ID NOW RSV
Mexico·Clase II·III. DIAGNOSTIC AGENTS·ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.·Registered October 18, 2019ES UNA PRUEBA DE DIAGNÓSTICO IN VITRO MOLECULAR RÁPIDO QUE UTILIZA LA TECNOLOGÍA DE AMPLIFICACIÓN ISOTÉRMICA DE ÁCIDOS NUCLEICOS PARA LA DETECCIÓN CUALITATIVA DEL ARN VÍRICO DEL VIRUS SINCICIAL RESPIRATORIO (VSR) DE PACIENTES CON SIGNOS Y SÍNTOMAS DE INFE
IT IS A RAPID MOLECULAR IN VITRO DIAGNOSTIC TEST USING ISOTHERMAL NUCLEIC ACID AMPLIFICATION TECHNOLOGY FOR THE QUALITATIVE DETECTION OF RESPIRATORY SYNCYTIAL VIRUS (RSV) VIRAL RNA FROM PATIENTS WITH SIGNS AND SYMPTOMS OF INFE
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA MOLECULAR RÁPIDA PARA LA DETECCIÓN DE ARN VIRAL DEL VIRUS SINCICIAL RESPIRATORIO (RSV).
- Trade Name (English)
- RAPID MOLECULAR TEST FOR THE DETECTION OF RESPIRATORY SYNCYTIAL VIRUS (RSV) VIRAL RNA.
- Analysis ID
- 2017R2019 SSA
- Registration Date
- October 18, 2019
- Name (Spanish)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
- Name (English)
- ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for ID NOW RSV (ID NOW RSV) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2017R2019 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on October 18, 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.