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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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Knieorthese 4-Punkt — 13 UDI-DI variants, MDR (Achim Ruthner GmbH)

MD Atlas
Achim Ruthner GmbH

Data from EUDAMED, last updated May 23, 2026

Knieorthese 4-Punkt

4251746617113XJ

13 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: 4251746617113XJ
Device name: Knieorthese 4-Punkt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRNPBHXSYTV4CDTP13DGRVXF

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

237104251746617113
237704251746617175
237404251746617144
238104251746617236
238004251746617229
237504251746617151
237204251746617120
237604251746617168
238404251746617274
237304251746617137
238204251746617243
238304251746617250
904251746617106