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HEMOSIL ACUSTAR ANTI-CARDIOLIPIN IGG CONTROLS - INVIMA Registration 2e1b7fa8e03c635677837a3ca93f9a3e

Access comprehensive regulatory information for HEMOSIL ACUSTAR ANTI-CARDIOLIPIN IGG CONTROLS (HEMOSIL ACUSTAR ANTI-CARDIOLIPIN IGG CONTROLS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 2e1b7fa8e03c635677837a3ca93f9a3e and manufactured by WERFEN COLOMBIA SAS. The device was registered on September 16, 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
2e1b7fa8e03c635677837a3ca93f9a3e
HEMOSIL ACUSTAR ANTI-CARDIOLIPIN IGG CONTROLS
INVIMA Analysis ID: 2e1b7fa8e03c635677837a3ca93f9a3e
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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
2e1b7fa8e03c635677837a3ca93f9a3e
Expire Date
September 16, 2031
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA SAS
Name (English)
THROW COLOMBIA SAS