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M-Series Bariatric Patient Lifter

by Savaria Concord Lifts 11 variants

Ref MBA454-1012-02-EUModel M-Series Bariatric

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0688503BARIATRICAK Basic UDI-DI 10688503001471UDI-DIDate23 Apr 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  • Withdrawn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
M-Series Bariatric Patient Lifter
Model / Reference
M-Series Bariatric, MBA454-1012-02-EU
Primary DI / UDI-DI
10688503001471
Basic UDI-DI
0688503BARIATRICAK
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