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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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Organization name
UDI-DI code
Reference / catalog number

71723 — Class I MDR by HOYER GmbH

MD Atlas
HOYER GmbH

EUDAMED last updated this device on Feb 13, 2026

71723

426074102ZubehoerH3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HOYER GmbH
UDI-DI code: 04260741020521
Reference / catalog number: 71723

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Manufacturer information

Organization name: HOYER GmbH
SRN: DE-MF-000007883
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260741020521
Basic UDI-DI: 426074102ZubehoerH3
Reference / catalog number: 71723
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Kreuzbügel (mit Axial-Drehlager für Deckenlifter) , schräge Form mit Vierpunktaufhängung (Haken jeweils an den Ecken), GRÖSSE L , Länge 55cm x Breite 27,5 cm, pulverbeschichtet RAL 9005 schwarz
Additional information URL: http://hoyer-lifter.com/kreuzbuegel-mit-vierpunktaufhaengung.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050399PATIENT TRANSFER LIFTS - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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