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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

91481 — Class I MDR by HOYER GmbH

MD Atlas
HOYER GmbH

EUDAMED last updated this device on May 12, 2026

91481

42607410291XXXTuch75

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HOYER GmbH
UDI-DI code: 04260741024697
Reference / catalog number: 91481

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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.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260741024697
Basic UDI-DI: 42607410291XXXTuch75
Reference / catalog number: 91481
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: Spezialsitz einteilig (Segeltuch - luftdurchlässig) komplett mit AD-Fell ausgeschlagen , leicht im Sitzen anlegbar, mit variablen Gurtschlaufen (ohne Metall) - ÜBERGRÖSSE / Größe : XL
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0805038002NON-RIGID SUPPORTS FOR LIFTS (HARNESSES)

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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Expiration date
Manufacturing date
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Software identification