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VIDAS D-DIMER EXCLUSION II (DEX2) - INVIMA Registration dcb4de0f5ddaef50104497f1cefe9f1e

Access comprehensive regulatory information for VIDAS D-DIMER EXCLUSION II (DEX2) (VIDAS D-DIMER EXCLUSION II (DEX2)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID dcb4de0f5ddaef50104497f1cefe9f1e and manufactured by BIOMร‰RIEUX S.A. The device was registered on August 17, 2027.

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
II
dcb4de0f5ddaef50104497f1cefe9f1e
VIDAS D-DIMER EXCLUSION II (DEX2)
INVIMA Analysis ID: dcb4de0f5ddaef50104497f1cefe9f1e
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Product Use / Uso del Producto
Spanish

ES UNA PRUEBA CUANTITATIVA AUTOMATIZADA EN LOS INSTRUMENTOS DE LA FAMILIA VIDAS QUE PERMITE LA VALORACION INMUNOENZIMATICA DE LOS PRODUCTOS DE DEGRADACION DE LA FIBRINA (FBDP) EN PLASMA HUMANO CON LA TECNICA ELFA.

English

IT IS AN AUTOMATED QUANTITATIVE TEST IN THE INSTRUMENTS OF THE VIDAS FAMILY THAT ALLOWS THE IMMUNOENZYMATIC ASSESSMENT OF FIBRIN DEGRADATION PRODUCTS (FBDP) IN HUMAN PLASMA WITH THE ELF TECHNIQUE.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
dcb4de0f5ddaef50104497f1cefe9f1e
Expire Date
August 17, 2027
Authorized Company / Fabricante
Name (Spanish)
BIOMร‰RIEUX S.A
Name (English)
BIOMร‰RIEUX S.A