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QUANTA FLASH® RF IGM REAGENTS - INVIMA Registration 5a5f9e812e017eb7a55949959c5c0b6e

Access comprehensive regulatory information for QUANTA FLASH® RF IGM REAGENTS (QUANTA FLASH® RF IGM REAGENTS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 5a5f9e812e017eb7a55949959c5c0b6e and manufactured by WERFEN COLOMBIA S.A.S. The device was registered on March 29, 2033.

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
5a5f9e812e017eb7a55949959c5c0b6e
QUANTA FLASH® RF IGM REAGENTS
INVIMA Analysis ID: 5a5f9e812e017eb7a55949959c5c0b6e
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Product Use / Uso del Producto
Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS_x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALITOS_x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
5a5f9e812e017eb7a55949959c5c0b6e
Expire Date
March 29, 2033
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA S.A.S
Name (English)
THROW COLOMBIA S.A.S