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MONA, Modell EL 200-120 Akku

by BEKA-Hospitec GmbH

Ref K126 BEKA ANA & MONA Pflege-&VersorgungsliegenModel K126 BEKA Pflege- und Versorgungsliegen und deren Zubehör

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426068189126BZ Basic UDI-DI 04260713252028UDI-DIDate10 Apr 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Ana El 100-80
Model / Reference
K126 BEKA Pflege- und Versorgungsliegen und deren Zubehör, K126 BEKA ANA & MONA Pflege-&Versorgungsliegen
Primary DI / UDI-DI
04260713252028
Basic UDI-DI
426068189126BZ
Direct Marketing DI
04260713252028
EMDN Code
Y1803 Assistive tables
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000013895

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See all devices from BEKA Hospitec GmbH →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No