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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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Rückenbandagen — 6 UDI-DI variants, MDR (Achim Ruthner GmbH)

MD Atlas
Achim Ruthner GmbH

Data from EUDAMED, last updated May 23, 2026

Rückenbandagen

42517466007N9

6 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: 42517466007N9
Device name: Rückenbandagen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 21, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01FYPFQYX8K2X3PNJX85H1WWA1

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

40030230404251746611029
40030230504251746611036
40030230604251746611043
40030230804251746611067
40030230904251746611074
40030230704251746611050