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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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Bandagen-Familie — 13 UDI-DI variants, MDR (WUNDmed GmbH & Co. KG)

MD Atlas
WUNDmed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Bandagen-Familie

426020662shb6HR

13 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: WUNDmed GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426020662shb6HR
Device name: Bandagen-Familie
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 9, 2022

Manufacturer & authorised representative

Manufacturer

Name: WUNDmed GmbH & Co. KG
SRN: DE-MF-000010322
Country: Germany
Email: verkauf@wundmed.de

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FVCFP9Z9FSWHRKDR57BRC6M4

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

04-00704260206625834
03-01004260206625322
04-00804260206622116
02-10304260206622086
02-09204260206624059
04-01604260206620167
04-01404260206620143
04-01504260206620150
04-02804260206620440
04-02704260206620433
04-02604260206620426
04-02404260206620242
04-02304260206620235