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FTD VIRAL MENINGITIS - INVIMA Registration 2873b23355973fa782c693ed7db9de25

Access comprehensive regulatory information for FTD VIRAL MENINGITIS (FTD VIRAL MENINGITIS) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 2873b23355973fa782c693ed7db9de25 and manufactured by SIEMENS HEALTHCARE S.A.S..

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
III
2873b23355973fa782c693ed7db9de25
FTD VIRAL MENINGITIS
INVIMA Analysis ID: 2873b23355973fa782c693ed7db9de25
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Product Use / Uso del Producto
Spanish

FTD VIRAL MENINGITIS ES UNA PRUEBA CUALITATIVA DE _x000D_ AMPLIFICACIÓN DE ÁCIDOS NUCLEICOS IN VITRO PARA LA _x000D_ DETECCIÓN Y LA DIFERENCIACIÓN DE ÁCIDOS NUCLEICOS _x000D_ VÍRICOS ESPECÍFICOS EN LÍQUIDO CEFALORRAQUÍDEO (LCR)_x000D_ DE ORIGEN HUMANO. LA PRUEBA ESTÁ CONCEBIDA COMO_x000D_ UNA AYUDA PARA EL DIAGNÓSTICO DE INFECCIONES _x000D_ CAUSADAS POR VIRUS DEL HERPES SIMPLE 1 Y 2 (HSV-1 Y _x000D_ HSV-2), VIRUS DE PAPERAS (MUV), VIRUS DE VARICELA _x000D_ ZÓSTER (VZV), ENTEROVIRUS (EV) Y PARECOVIRUS _x000D_ HUMANO (HPEV). PARA USO DIAGNÓSTICO IN VITRO.

English

FTD VIRAL MENINGITIS IS A QUALITATIVE _x000D_ TEST IN VITRO NUCLEIC ACID AMPLIFICATION FOR _x000D_ NUCLEIC ACID DETECTION AND DIFFERENTIATION _x000D_ SPECIFIC VIRAL CASES IN CEREBROSPINAL FLUID (CSF)_x000D_ OF HUMAN ORIGIN. THE TEST IS DESIGNED COMO_x000D_ AN AID FOR THE DIAGNOSIS OF _x000D_ INFECTIONS CAUSED BY HERPES SIMPLEX VIRUS 1 AND 2 (HSV-1 AND _x000D_ HSV-2), MUMPS VIRUS (MUV), CHICKENPOX VIRUS, _x000D_ ZOSTER (VZV), ENTEROVIRUS (EV), AND PARECOVIRUS _x000D_ HUMAN (HPEV). FOR IN VITRO DIAGNOSTIC USE.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
2873b23355973fa782c693ed7db9de25
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE S.A.S.