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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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Standard performance leikkaustakki — 5 UDI-DI variants, MDR

MD Atlas
Image Wear Oy

Data from EUDAMED, last updated May 23, 2026

Standard performance leikkaustakki

64180104F013A24JU

5 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: Image Wear Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 64180104F013A24JU
Device name: Standard performance leikkaustakki
Device model: 4F013
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 21, 2021

Manufacturer & authorised representative

Manufacturer

Name: Image Wear Oy
SRN: FI-MF-000018231
Country: Finland
Email: imagewear@imagewear.fi

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FQEJAGPRRKJ0GXTNR0HH2Q9G

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

4F013A24560L06418010344702
4F013A24560XL06418010344719
4F013A24560S06418010344689
4F013A24560XXL06418010344726
4F013A24560M06418010344696