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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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Tukan — 6 UDI-DI variants, MDR (Wolturnus A/S)

MD Atlas
Wolturnus A/S

Data from EUDAMED, last updated May 31, 2026

Tukan

57138250087W

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: Wolturnus A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57138250087W
Device name: Tukan
Device model: Tukan
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 18, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01JY0W7HK2TEHQZTJY1B8QNM08

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

Tukan05713825642595
Tukan B05713825642601
Tukan C05713825642618
Tukan D05713825642625
Tukan SL05713825642632
Tukan Tilt05713825642649