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QUANTA FLASH® H-TTG IGA REAGENTS - INVIMA Registration 26de2a1b6a26282da90627236d9ba5fe

Access comprehensive regulatory information for QUANTA FLASH® H-TTG IGA REAGENTS (QUANTA FLASH® H-TTG IGA REAGENTS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 26de2a1b6a26282da90627236d9ba5fe and manufactured by WERFEN COLOMBIA S.A.S. The device was registered on September 09, 2031.

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
26de2a1b6a26282da90627236d9ba5fe
QUANTA FLASH® H-TTG IGA REAGENTS
INVIMA Analysis ID: 26de2a1b6a26282da90627236d9ba5fe
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Product Use / Uso del Producto
Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO._x000D_

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE ORGANISM HUMANO._x000D_

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
26de2a1b6a26282da90627236d9ba5fe
Expire Date
September 09, 2031
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA S.A.S
Name (English)
THROW COLOMBIA S.A.S