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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

72020 — Class I MDR by HOYER GmbH

MD Atlas
HOYER GmbH

EUDAMED last updated this device on Jan 20, 2026

72020

426074102720XXPocket3J

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HOYER GmbH
UDI-DI code: 04260741020323
Reference / catalog number: 72020

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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: 04260741020323
Basic UDI-DI: 426074102720XXPocket3J
Reference / catalog number: 72020
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: HOYER-Pocketlift - leicht transportabler Deckenlift zur Benutzung in verschiedenen Räumen - (ohne Fahrmotor), Hubleistung 130 kg, mit elektrischer u. mechanischer Notabsenkung, Not-Aus, Akkuvollversorgung u. Ladegerät (24V), elektrisch heben u. senken, von Hand fahren, komplett mit einem Fahrwerk u. Fahrwerksgurt 71046 , HMV.- Nr.: 22.40.03.0000
Additional information URL: http://hoyer-lifter.com/pocketlift.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050302ELECTRIC FIXED LIFTS

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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