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ATELLICA IM ATGII QUALITY CONTROL (ATGII QC) - INVIMA Registration e9d5478cdf21e2e133091d4b78292410

Access comprehensive regulatory information for ATELLICA IM ATGII QUALITY CONTROL (ATGII QC) (ATELLICA IM ATGII QUALITY CONTROL (ATGII QC)) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID e9d5478cdf21e2e133091d4b78292410 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
e9d5478cdf21e2e133091d4b78292410
ATELLICA IM ATGII QUALITY CONTROL (ATGII QC)
INVIMA Analysis ID: e9d5478cdf21e2e133091d4b78292410
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Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
e9d5478cdf21e2e133091d4b78292410
Expire Date
January 29, 2031
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE SAS