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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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Compression sock — 11 UDI-DI variants, MDR (Wiges AB)

MD Atlas
Wiges AB

Data from EUDAMED, last updated May 30, 2026

Compression sock

73325975329T4

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: Wiges AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73325975329T4
Device name: Compression sock
Device model: 5329
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Wiges AB
SRN: SE-MF-000007713
Country: Sweden
Email: info@wiges.se
Phone: +46 320 21 05 99

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JP074WWHPPGTQMDSX95ZJNV6

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

53290211207332597820987
53290241407332597839118
53290211307332597820994
53290241307332597839101
53290211407332597821007
53290441207332597819110
53290381307332597831655
53290241207332597839095
53290441407332597819134
53290441307332597819127
53290381407332597831662