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ATELLICA IM CPSA QC (QUALITY CONTROL MATERIAL) - INVIMA Registration 05f5cb7b0d9665228664fb8354c98f55

Access comprehensive regulatory information for ATELLICA IM CPSA QC (QUALITY CONTROL MATERIAL) (ATELLICA IM CPSA QC (QUALITY CONTROL MATERIAL)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 05f5cb7b0d9665228664fb8354c98f55 and manufactured by SIEMENS HEALTHCARE SAS. The device was registered on December 03, 2028.

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
05f5cb7b0d9665228664fb8354c98f55
ATELLICA IM CPSA QC (QUALITY CONTROL MATERIAL)
INVIMA Analysis ID: 05f5cb7b0d9665228664fb8354c98f55
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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
05f5cb7b0d9665228664fb8354c98f55
Expire Date
December 03, 2028
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE SAS