98292d5b426b11f7de46efcf791d2f8f

REAGENT PACK HUMALYTE PLUS 3

HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH·II·Colombia INVIMA·Expires August 12, 2031

Device classification

Risk class / Clase de Riesgo: II
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: 98292d5b426b11f7de46efcf791d2f8f
Expire date: August 12, 2031

Authorized company / Fabricante

Name (Spanish): HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH
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 REAGENT PACK HUMALYTE PLUS 3 (REAGENT PACK HUMALYTE PLUS 3) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 98292d5b426b11f7de46efcf791d2f8f and manufactured by HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH. The device was registered on August 12, 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.