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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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Sängynjalankorottaja — 8 UDI-DI variants, MDR (Tukimet Oy)

MD Atlas
Tukimet Oy

Data from EUDAMED, last updated May 23, 2026

Sängynjalankorottaja

6430057234010TQ

8 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: 6430057234010TQ
Device name: Sängynjalankorottaja
Device model: 4010
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 15, 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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FMHD7HKZANC1N9E1PT9XPQ13

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

65012906430057230589
65011906430057230558
65012806430057230565
65010506430057230534
65010606430057230541
65013006430057230572
650129S06430057230602
650129SV06430057230596