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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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Organization name
UDI-DI code
Reference / catalog number

7.12.28 — Class IIa MDR by ID Information und…

MD Atlas
ID Information und Dokumentation im Gesundheitswesen GmbH & Co. KGaA

EUDAMED last updated this device on Aug 27, 2025

7.12.28

426072006030246260IDCCC2T

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ID Information und Dokumentation im Gesundheitswesen GmbH & Co. KGaA
UDI-DI code: 42607200600748
Reference / catalog number: 7.12.28

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Manufacturer information

Organization name: ID Information und Dokumentation im Gesundheitswesen GmbH & Co. KGaA
SRN: DE-MF-000007371
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Aug 7, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 42607200600748
Basic UDI-DI: 426072006030246260IDCCC2T
Reference / catalog number: 7.12.28
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: ID clinical context coding inklusive dem Modul ID DASHBOARD - nachfolgend als ID CCC genannt - ist eine Softwarelösung zur Unterstützung der stationären Behandlung und zur Verbesserung der Kodierqualität. Die Softwarelösung darf fallbegleitend - während der Patient stationär behandelt wird - eingesetzt werden.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

ID clinical context coding (ID CCC)426072006030246260IDCCC2TOn the market ab 7.13.0426072006030246260IDCCC2TOn the market ab 7.12.30426072006030246260MDXBQOn the market ab 7.11.22426072006030246260MDXBQOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.