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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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Kävelyapuväline — 11 UDI-DI variants, MDR (Tukimet Oy)

MD Atlas
Tukimet Oy

Data from EUDAMED, last updated May 23, 2026

Kävelyapuväline

6430057233030TP

11 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: Tukimet Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6430057233030TP
Device name: Kävelyapuväline
Device model: 3030
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 9, 2021

Manufacturer & authorised representative

Manufacturer

Name: Tukimet Oy
SRN: FI-MF-000006700
Country: Finland
Email: tukimet@tukimet.fi
Phone: +35826774222

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FKNDZPHTY3109WY0BHTAEHX2

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

338700L06430057230848
338700LKY06430057230886
33960006430057230008
339600L06430057230039
339600LM06430057230053
339600M06430057230022
33870006430057230015
338700i06430057230046
338700M06430057230978
33890006430057231357
338900M06430057231364