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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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Bügel — 14 UDI-DI variants, MDR (HOYER GmbH)

MD Atlas
HOYER GmbH

Data from EUDAMED, last updated May 23, 2026

Bügel

426074102ZubehoerH3

14 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: HOYER GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074102ZubehoerH3
Device name: Bügel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: HOYER GmbH
SRN: DE-MF-000007883
Country: Germany
Email: info@hoyer-lifter.com
Phone: +49 6033 96520

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGPZPQ7VPAT2ETCMQE69DN2D

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

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7150604260741020491
7149804260741020507
9221004260741022341
9220104260741022334
9357404260741024949
9351504260741022365
7161704260741020484
7172304260741020521
7172204260741020514
9225104260741022433
9225004260741022426
9206204260741022310
9223804260741024543