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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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Flexible Endoscopes / Flexible Endoskope — 4 UDI-DI variants, MDR

MD Atlas
EndoMed Systems GmbH

Data from EUDAMED, last updated May 23, 2026

Flexible Endoscopes / Flexible Endoskope

42512867001M3

4 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: EndoMed Systems GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 42512867001M3
Device name: Flexible Endoscopes / Flexible Endoskope
Device model: COMBO 3 Gastroscope G34Q / COMBO 3 Gastroscope G34 / COMBO 3 Colonoscope C34S / COMBO 3 Colonoscope C34L
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 1, 2023

Manufacturer & authorised representative

Manufacturer

Name: EndoMed Systems GmbH
SRN: DE-MF-000015581
Country: Germany
Email: info@endomed.com
Phone: +49 751 35978 0

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01H6R942NGWT64CTCWEAN0KYN8

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

60016104251286706094
60017004251286700030
60017104251286700047
60016004251286706087