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triLift

by Pollogen Ltd

Ref 30020110Model triLift 2.0 Body upgrade

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-17290016586777 Basic UDI-DI 17290016586777UDI-DIDate4 Aug 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
triLift 2.0
Model / Reference
triLift 2.0 Body upgrade, 30020110
Primary DI / UDI-DI
17290016586777
Basic UDI-DI
B-17290016586777
EMDN Code
Z12040280 General medicine therapeutic treatment instruments - hardware accessories
Device Class
Class IIb
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
IL-MF-000031034
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Pollogen Ltd

See all devices from Pollogen Ltd →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No