7f6abd71b9c4aaf691de6977e7e64514

IMTEC-ANA SCREEN

HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH·II·Colombia INVIMA·Expires January 27, 2032
Device classification
Risk class / Clase de Riesgo
II
Product type (Spanish)
REACTIVO DIAGNOSTICO
Product type (English)
DIAGNOSTIC REAGENT
Registration information
Analysis ID
7f6abd71b9c4aaf691de6977e7e64514
Expire date
January 27, 2032
Authorized company / Fabricante
Name (English)
HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH
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 IMTEC-ANA SCREEN (IMTEC-ANA SCREEN) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 7f6abd71b9c4aaf691de6977e7e64514 and manufactured by HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH. The device was registered on January 27, 2032.

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.