081110fa64e03bb3cd683432145fc7e5

HUMAN CHORIONIC GONADOTROPIN (HCG) TEST

DIAGNOSTILAB VM SAS·II·Colombia INVIMA·Expires May 19, 2031

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

Product use / Uso del Producto

Spanish

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

English

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

About this record

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.