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Manual Bed

by Hong Ky Co., Ltd. 4 variants

Ref 9547

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 Number893620620MB9XXXHA Basic UDI-DI 08936206201243UDI-DIDate19 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Manual Bed
Model / Reference
9547
Primary DI / UDI-DI
08936206201243
Basic UDI-DI
893620620MB9XXXHA
Direct Marketing DI
08936206201243
EMDN Code
V080602 Manual medical beds
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
VN-MF-000011592
Authorised representative
KOMAS Medical Technology GmbH DE-AR-000045617

Other devices from Hong Ky Co., Ltd.

See all devices from Hong Ky Co., Ltd. →

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