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AMH HUMACLIA SR - INVIMA Registration e6ed0a89e88d4c32fad8e72abe9a7aa2

Access comprehensive regulatory information for AMH HUMACLIA SR (AMH 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 e6ed0a89e88d4c32fad8e72abe9a7aa2 and manufactured by HUMAN GESELLSCHAFT FรœR BIOCHEMICA UND DIAGNOSTICA MBH. The device was registered on November 26, 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
e6ed0a89e88d4c32fad8e72abe9a7aa2
AMH HUMACLIA SR
INVIMA Analysis ID: e6ed0a89e88d4c32fad8e72abe9a7aa2
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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
e6ed0a89e88d4c32fad8e72abe9a7aa2
Expire Date
November 26, 2031
Authorized Company / Fabricante
Name (English)
HUMAN GESELLSCHAFT FรœR BIOCHEMICA UND DIAGNOSTICA MBH