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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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Schulterfix — 14 UDI-DI variants, MDR (Achim Ruthner GmbH)

MD Atlas
Achim Ruthner GmbH

Data from EUDAMED, last updated May 23, 2026

Schulterfix

42517466055NL

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: Achim Ruthner GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42517466055NL
Device name: Schulterfix
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 24, 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

14 UDI-DI variants

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Applied filters

basicUdiUlid01FYXG8Y900SPJ73EQQR06Z9BC

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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52310020604251746607152
52310010604251746607114
52324810604251746607190
52324820404251746607213
52310020404251746607145
52324810404251746607183
52310010404251746607107
52324820304251746607206
52310020304251746607138
52324810304251746607176
52310010304251746607091
52310020804251746607169
52310010804251746607121