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AFP HUMACLIA SR - INVIMA Registration 12e0c613b5a07339ed0181ef5e18572c

Access comprehensive regulatory information for AFP HUMACLIA SR (AFP HUMACLIA SR ) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 12e0c613b5a07339ed0181ef5e18572c and manufactured by HUMAN GESELLSCHAFT FรœR BIOCHEMICA UND DIAGNOSTICA MBH. The device was registered on November 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.

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INVIMA Official Data
II
12e0c613b5a07339ed0181ef5e18572c
AFP HUMACLIA SR
INVIMA Analysis ID: 12e0c613b5a07339ed0181ef5e18572c
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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
12e0c613b5a07339ed0181ef5e18572c
Expire Date
November 12, 2031
Authorized Company / Fabricante
Name (English)
HUMAN GESELLSCHAFT FรœR BIOCHEMICA UND DIAGNOSTICA MBH