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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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arthrosan Original — 53 UDI-DI variants, MDR (arthroven GmbH)

MD Atlas
arthroven GmbH

Data from EUDAMED, last updated May 23, 2026

arthrosan Original

42503080001b5B

53 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: arthroven GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503080001b5B
Device name: arthrosan Original
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: arthroven GmbH
SRN: DE-MF-000005542
Country: Germany
Email: info@arthroven.de
Phone: +4977202066020

Variants by status

UDI-DI variants

53 UDI-DI variants

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Applied filters

basicUdiUlid01KJYRMDXBGZZRVHJK7JHE8DBY

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

ARSL 4804250308747176
ARSR 3704250308747213
ARSKL 2204250308704315

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