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Lingkeci

by Guangdong Lingkeci Technology Co., Ltd. 2 variants

Ref LEADER BED ⅠModel LEADER BED Ⅰ、LEADER BED Ⅱ、LEADER BED III、LEADER BED Ⅳ

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 linked in EUDAMED

A group certificate may exist

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 Number697665456MsickbedBA Basic UDI-DI 06976654560020UDI-DIDate1 Mar 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Manual sickbed
Model / Reference
LEADER BED Ⅰ、LEADER BED Ⅱ、LEADER BED III、LEADER BED Ⅳ, LEADER BED Ⅰ
Primary DI / UDI-DI
06976654560020
Basic UDI-DI
697665456MsickbedBA
EMDN Code
V08050101 Generic use stretchers
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000038655
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Guangdong Lingkeci Technology Co., Ltd.

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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