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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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W5 — 9 UDI-DI variants, MDR (Wolturnus A/S)

MD Atlas
Wolturnus A/S

Data from EUDAMED, last updated May 31, 2026

W5

57138250077U

9 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: Wolturnus A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57138250077U
Device name: W5
Device model: W5
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: Wolturnus A/S
SRN: DK-MF-000025274
Country: Denmark
Email: info@wolturnus.dk

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01JQTM7QCAREHX6RDCDJAGP3A4

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

W505713825642656
W5 D05713825642670
W5 Junior05713825642687
W5 K05713825642694
W5 S05713825642700
W5 SL05713825642717
W5 Suspension05713825642724
W5 Suspension XXL05713825642212
W5 XXL05713825642731