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HUMAN CHORIONIC GONADOTROPIN (HCG) TEST - INVIMA Registration 081110fa64e03bb3cd683432145fc7e5

Access comprehensive regulatory information for HUMAN CHORIONIC GONADOTROPIN (HCG) TEST (HUMAN CHORIONIC GONADOTROPIN (HCG) TEST) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 081110fa64e03bb3cd683432145fc7e5 and manufactured by DIAGNOSTILAB VM SAS. The device was registered on May 19, 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
081110fa64e03bb3cd683432145fc7e5
HUMAN CHORIONIC GONADOTROPIN (HCG) TEST
INVIMA Analysis ID: 081110fa64e03bb3cd683432145fc7e5
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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
081110fa64e03bb3cd683432145fc7e5
Expire Date
May 19, 2031
Authorized Company / Fabricante
Name (Spanish)
DIAGNOSTILAB VM SAS
Name (English)
DIAGNOSTILAB VM SAS