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IGE KIT FOR USE ON SPAPLUS - INVIMA Registration b99d14d0378d150e9983b1dd0e62ae37

Access comprehensive regulatory information for IGE KIT FOR USE ON SPAPLUS (IGE KIT FOR USE ON SPAPLUS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID b99d14d0378d150e9983b1dd0e62ae37 and manufactured by QUIMIOLAB S.A.S. The device was registered on November 11, 2030.

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
b99d14d0378d150e9983b1dd0e62ae37
IGE KIT FOR USE ON SPAPLUS
INVIMA Analysis ID: b99d14d0378d150e9983b1dd0e62ae37
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
b99d14d0378d150e9983b1dd0e62ae37
Expire Date
November 11, 2030
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.S
Name (English)
QUIMIOLAB S.A.S