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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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Fußabduktionsschiene — 5 UDI-DI variants, MDR (Semeda GmbH)

MD Atlas
Semeda GmbH

Data from EUDAMED, last updated May 23, 2026

Fußabduktionsschiene

426020155FASZBSXV

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: Semeda GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426020155FASZBSXV
Device name: Fußabduktionsschiene
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Semeda GmbH
SRN: DE-MF-000008334
Country: Germany
Email: qm-ek@semeda.de
Phone: 0049-5824-98555-0

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FVHN1MK8DK4ZXSDTDSAMV23W

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

ALFA-Flex Brace Foot Abduction Brace04260201550025
ALFA-Flex Light Brace Foot Abduction Brace04260201551312
ALFA-Flex XL Brace Foot Abduction Brace04260201550049
BETA-Flex Brace Foot Abduction Brace04260201551305
ECO-Brace Light Foot Abduction Brace04260201550872