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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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Bodenlift Zubehör — 9 UDI-DI variants, MDR (HOYER GmbH)

MD Atlas
HOYER GmbH

Data from EUDAMED, last updated May 23, 2026

Bodenlift Zubehör

426074102BLZubehoerES

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: HOYER GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074102BLZubehoerES
Device name: Bodenlift Zubehör
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 20, 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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KHWXYX40SPYVXKC6Z889ZC25

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

9221504260741024192
9348304260741022358
9221804260741022396
9224204260741022402
9224304260741022419
9111904260741024222
9330204260741020828
9349604260741024093
9346004260741020873