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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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Registrierpapiere (EKG, CTG und EEG)… — 14 UDI-DI variants, MDR

MD Atlas
Diagramm Halbach GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Registrierpapiere (EKG, CTG und EEG) ohne Messfunktion

42501236700200CR

14 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Diagramm Halbach GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42501236700200CR
Device name: Registrierpapiere (EKG, CTG und EEG) ohne Messfunktion
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: Diagramm Halbach GmbH & Co. KG
SRN: DE-MF-000012732
Country: Germany
Email: info@halbach.com
Phone: +49 2304 7590

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01K5TYZA7ZR72JNCHMQTWJSZZN

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

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72640004250123605767
71613804250123600052
71683004250123603046
72508004250123603572
71572004250123602803
71571004250123602797
71650804250123602964
72600204250123600601
72703004250123600625
71651904250123600656
72604004250123603640
71651804250123600595
74747104250123603763