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HUMANEX A1C VARIANT REAGENT - INVIMA Registration b6e7fc7733b9f6d46bfa2ebb48baccac

Access comprehensive regulatory information for HUMANEX A1C VARIANT REAGENT (HUMANEX A1C VARIANT REAGENT) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID b6e7fc7733b9f6d46bfa2ebb48baccac and manufactured by HUMAN GESELLSCHAFT FรœR BIOCHEMICA UND DIAGNOSTICA MBH. The device was registered on December 13, 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.

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INVIMA Official Data
II
b6e7fc7733b9f6d46bfa2ebb48baccac
HUMANEX A1C VARIANT REAGENT
INVIMA Analysis ID: b6e7fc7733b9f6d46bfa2ebb48baccac
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
b6e7fc7733b9f6d46bfa2ebb48baccac
Expire Date
December 13, 2032
Authorized Company / Fabricante
Name (English)
HUMAN GESELLSCHAFT FรœR BIOCHEMICA UND DIAGNOSTICA MBH