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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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Kinesiologie-Tape — 9 UDI-DI variants, MDR (WUNDmed GmbH & Co. KG)

MD Atlas
WUNDmed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Kinesiologie-Tape

426020662kt3JR

9 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: 426020662kt3JR
Device name: Kinesiologie-Tape
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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FVCEP1FY5899K2QBMDJ7P99Q

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

02-12804260206626619
04-04104260206625360
04-03904260206625346
04-04804260206626664
04-04004260206625353
04-04904260206626671
04-04704260206626657
04-03804260206625339
04-05004260206626688