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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

42 700022298LiegenFM — Class I MDR by Becker GmbH

MD Atlas
Becker GmbH

EUDAMED last updated this device on Dec 12, 2025

42 700022298LiegenFM

42700022298LiegenFM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Becker GmbH
UDI-DI code: 04270002229815
Reference / catalog number: 42 700022298LiegenFM

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Manufacturer information

Organization name: Becker GmbH
SRN: DE-MF-000029840
Manufacturer status: Active

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: 04270002229815
Basic UDI-DI: 42700022298LiegenFM
Reference / catalog number: 42 700022298LiegenFM
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: Die elektrisch höhenverstellbare „Lisa“ und „Pia“ von BECKER® Therapieliege, kombiniert mit dem optionalem Innocare-Lagerungssystem®, ist für den Einsatz im häuslichen, stationären, ambulanten und schulischen Bereich konzipiert. Weitere Funktionen der Therapieliege: - Positionierung/ Lagerung von Körperabschnitten wie Kopf, Rumpf und Extremitäten in therapeutisch sinnvoller Stellung - Teilentlastung einzelner Körperabschnitte, vorzugsweise bei Vorliegen von komplexen Behinderungsbildern - Förderung der Eigen-/ Körperwahrnehmung - Linderung von Schmerzen verursacht durch eine Fehlhaltung - Weichlagerung - Entspannung/ Regulation des Muskeltonus - Einsatz bei beginnender und/ oder vorhandenen Kontrakturen - Sichere und stabile Position im Sitzen sowie Liegen für die Teilnahme an Aktivitäten des öffentlichen Lebens
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y1803ASSISTIVE TABLES

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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

42 700022298LiegenFM42700022298LiegenFMOn the market 42 700022298LagerungZU42700022298LagerungZUOn the market 42 700022298CaroP842700022298CaroP8On the market

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.