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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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contextflow ADVANCE Chest CT — 8 UDI-DI variants, MDR

MD Atlas
contextflow GmbH

Data from EUDAMED, last updated May 23, 2026

contextflow ADVANCE Chest CT

912010733CFACHESTCT6J

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: contextflow GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 912010733CFACHESTCT6J
Device name: contextflow ADVANCE Chest CT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Dec 28, 2022

Manufacturer & authorised representative

Manufacturer

Name: contextflow GmbH
SRN: AT-MF-000001773
Country: Austria
Email: office@contextflow.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GNCY3HS24GFV1N7WZ0PPRC0M

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

contextflow ADVANCE Chest CT09120107330167
contextflow ADVANCE Chest CT09120107330143
contextflow ADVANCE Chest CT09120107330082
contextflow ADVANCE Chest CT09120107330099
contextflow ADVANCE Chest CT 2.009120107330075
contextflow ADVANCE Chest CT09120107330105
3.2.009120107330112
3.109120107330129