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Floor Lift, Portable Floor Lift

by Intradin (Shanghai) Machinery Co., Ltd. 3 variants

Ref ATD102,GEUTS102Model ATD101, GEUTS101 ATD102, GEUTS102 ATD103, GEUTS103

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69439407FloorLiftXN Basic UDI-DI 06943940700071UDI-DIDate4 Nov 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  • Withdrawn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
Floor Lift, Portable Floor Lift
Model / Reference
ATD101, GEUTS101 ATD102, GEUTS102 ATD103, GEUTS103, ATD102, GEUTS102
Primary DI / UDI-DI
06943940700071
Basic UDI-DI
69439407FloorLiftXN
EMDN Code
V08050302 Electric fixed lifts
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000034847
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Intradin (Shanghai) Machinery Co., Ltd

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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