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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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Knieschiene abwaschbar — 11 UDI-DI variants, MDR (Achim Ruthner GmbH)

MD Atlas
Achim Ruthner GmbH

Data from EUDAMED, last updated May 23, 2026

Knieschiene abwaschbar

42517466034NC

11 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: Achim Ruthner GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42517466034NC
Device name: Knieschiene abwaschbar
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: Achim Ruthner GmbH
SRN: DE-MF-000016101
Country: Germany
Email: info@ruthner-gmbh.de
Phone: +496272920510

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01FYRT19VQ7VQASX18ZG5PP5YG

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

23024830604251746602140
23024830504251746602133
23024830404251746602126
23024830704251746602157
23024830804251746602164
23034830604251746602195
23034830504251746602188
23034830404251746602171
23034830704251746602201
23034830804251746602218
23034830904251746602225