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Patient lift

by INTCO MEDICAL (HK) CO., ltd 6 variants

Ref Y403Model Y401 / Y402 / Y403 / Y407

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 Number489712866-0-PatientliftS7 Basic UDI-DI 04897128665916UDI-DIDate24 Jun 2025RegisteredStatusActive

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  • Withdrawn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
Patient Lifts
Model / Reference
Y401 / Y402 / Y403 / Y407, Y403
Primary DI / UDI-DI
04897128665916
Basic UDI-DI
489712866-0-PatientliftS7
Direct Marketing DI
04897128665916
EMDN Code
V0805030102 Electric mobile lifts
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000011338
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from INTCO MEDICAL (HK) CO., ltd

See all devices from INTCO MEDICAL (HK) 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