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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

90361 — Class I MDR by HOYER GmbH

MD Atlas
HOYER GmbH

EUDAMED last updated this device on Jan 21, 2026

90361

42607410290XXXPool64

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HOYER GmbH
UDI-DI code: 04260741020255
Reference / catalog number: 90361

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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: 04260741020255
Basic UDI-DI: 42607410290XXXPool64
Reference / catalog number: 90361
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 Pool-Butler „Stairless“, Schwimmbadlift zur Anwendung an Bodenbecken, Aufzustellen ohne Bohren oder Installationsarbeiten, Tragkraft 150 kg, Laufschienen aus Rundrohr, mit geradem Auslauf auf dem Beckenrand, Schlitten zur Aufnahme von Sitz (Sitz nicht im Lieferumfang enthalten), mit einer Wechselakkueinheit, inkl. Ladegerät, Basisanlage für eine Wassertiefe von 1,35m bis 1,50m, Laufschiene justierbar nach Angabe, Fahrweg 200 cm
Additional information URL: http://hoyer-lifter.com/pool-butler--stairless-.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050303BATH 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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