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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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Ankle Brace — 6 UDI-DI variants, MDR (Tischner & Thomann GmbH)

MD Atlas
Tischner & Thomann GmbH

Data from EUDAMED, last updated May 23, 2026

Ankle Brace

426069255AB0152

6 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: Tischner & Thomann GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426069255AB0152
Device name: Ankle Brace
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 9, 2022

Manufacturer & authorised representative

Manufacturer

Name: Tischner & Thomann GmbH
SRN: DE-MF-000027113
Country: Germany
Email: info@tischner-thomann.de

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GA108633Z11KX9G0P9S29MFZ

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

AB011242606925510820
AB01342700010823816
AB03242606925583572
AB03142606925583404
AB01242700010823748
AB0142700010823670