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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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CGM CLINICAL Assessments — 7 UDI-DI variants, MDR

MD Atlas
CompuGroup Medical Software GmbH

Data from EUDAMED, last updated May 23, 2026

CGM CLINICAL Assessments

426238198ASS-001AE

7 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: CompuGroup Medical Software GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426238198ASS-001AE
Device name: CGM CLINICAL Assessments
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: Aug 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: CompuGroup Medical Software GmbH
SRN: DE-MF-000027005
Country: Germany
Email: info.de@cgm.com
Phone: +49 261 8000-1780

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01GB7C337QZHKP3VJ0WHEHNG9M

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

3001552304262381980241
3001552304262381980234
3001552304262381980098
CGM CLINICAL Assessments04262381980265
3001552304262381980067
3001552304262381980029
3001552304262381980050