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M-Series Fixed Patient Lifter

by Savaria Concord Lifts 56 variants

Ref M929147Model M-Series

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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 Number0688503FIXEDLIFTJE Basic UDI-DI 10688503147001UDI-DIDate23 Apr 2025RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
M-Series Fixed Patient Lifter
Model / Reference
M-Series, M929147
Primary DI / UDI-DI
10688503147001
Basic UDI-DI
0688503FIXEDLIFTJE
EMDN Code
V08050302 Electric fixed lifts
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CA-MF-000010883
Authorised representative
Advena SRL IT-AR-000051131

Other devices from Savaria Concord Lifts

See all devices from Savaria Concord Lifts →

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