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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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ID Clinical Context Coding (ID CCC) — 3 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 23, 2026

ID Clinical Context Coding (ID CCC)

426072006030246260IDCCC2T

3 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: ID Information und Dokumentation im Gesundheitswesen GmbH & Co. KGaA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426072006030246260IDCCC2T
Device name: ID Clinical Context Coding (ID CCC)
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: Jan 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: ID Information und Dokumentation im Gesundheitswesen GmbH & Co. KGaA
SRN: DE-MF-000007371
Country: Germany
Email: info@id-berlin.de
Phone: +4930246260

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GQFH7TX2ZGE7TM0RR5D9F2H2

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

ID clinical context coding (ID CCC)42607200600298
7.12.2842607200600748
ab 7.13.042607200600984