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ADVIA CENTAUR ANDROSTENEDIONE (ANDRO) - INVIMA Registration aaaed79bf5a7db2d5e17bfe0cac25756

Access comprehensive regulatory information for ADVIA CENTAUR ANDROSTENEDIONE (ANDRO) (ADVIA CENTAUR ANDROSTENEDIONE (ANDRO) ) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID aaaed79bf5a7db2d5e17bfe0cac25756 and manufactured by SIEMENS HEALTHCARE SAS. The device was registered on January 29, 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
aaaed79bf5a7db2d5e17bfe0cac25756
ADVIA CENTAUR ANDROSTENEDIONE (ANDRO)
INVIMA Analysis ID: aaaed79bf5a7db2d5e17bfe0cac25756
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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
aaaed79bf5a7db2d5e17bfe0cac25756
Expire Date
January 29, 2031
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE SAS