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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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Rigid Endoscopes / Starre Endoskope — 8 UDI-DI variants, MDR

MD Atlas
EndoMed Systems GmbH

Data from EUDAMED, last updated May 23, 2026

Rigid Endoscopes / Starre Endoskope

42512867018ML

8 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: 42512867018ML
Device name: Rigid Endoscopes / Starre Endoskope
Device model: Hysteroscope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 11, 2024

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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HV6KVAXCRDMR0VPYCQJY7WGW

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

84100004251286700740
84104504251286700894
84104004251286700863
84104104251286700870
84103204251286700832
84103004251286700825
84100104251286700757
84104204251286700887