DIINSELDENGUENS1AGRAPIDTEST DEVICE
Mexico·Clase II·III. DIAGNOSTIC AGENTS·DIINSEL, S.A. DE C.V.·Registered May 12, 2022ELDISPOSITIVODIINSELDENGUENS1AGRAPIDTESTDEVICEDE PRUEBA RÁPIDA DENGUE NS1 AG (SANGREENTERA/SUERO/PLASMA) ES UN INMUNOENSAYOCROMATOGRÁFICO RÁPIDO PARA LA DETECCIÓNCUALITATIVADELANTÍGENONS1DELVIRUSDELDENGUEENSANGRE, SUERO O PLASMA HUMANO COMPLETO COMOAYUDAENELDIAGNÓSTICODEINFECCIONESDEDENGUEPRIMARIAS Y SECUNDARIAS
THE DIINSELDENGUENS1AGRAPIDTESTDEVICE RAPID DENGUE NS1 AG (WHOLE BLOOD/SERUM/PLASMA) RAPID TEST DEVICE IS A RAPID CHROMATOGRAPHIC IMMUNOASSAY FOR THE QUALITATIVE ADVANCE DETECTION1 OF DENGUE VIRUS IN BLOOD, SERUM OR WHOLE HUMAN PLASMA AS AN AID IN THE DIAGNOSIS OF PRIMARY AND SECONDARY DENGUE INFECTIONS
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA RÁPIDA PARADETECCIÓN DE DENGUE
- Trade Name (English)
- RAPID TEST FOR DENGUE DETECTION
- Analysis ID
- 361R2022 SSA
- Registration Date
- May 12, 2022
- Name (Spanish)
- DIINSEL, S.A. DE C.V.
- Name (English)
- DIINSEL, S.A. DE C.V.
Access comprehensive regulatory information for DIINSELDENGUENS1AGRAPIDTEST DEVICE (DIINSELDENGUENS1AGRAPIDTEST DEVICE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 361R2022 SSA and manufactured by DIINSEL, S.A. DE C.V.. The device was registered on May 12, 2022.
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.