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triLift

by Pollogen Ltd

Ref 30020100Model triLift

triLift (30020100) is a device classified as Class IIb in the EU and Class II in the US made by Pollogen Ltd, registered in EUDAMED on 4 Aug 2026 (Basic UDI-DI B-07290016586763) and listed in FDA GUDID since 2 Feb 2026 (UDI-DI 07290016586763), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-07290016586763 Basic UDI-DI 07290016586763UDI-DIDate4 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07290016586763 UDI-DI Date2 Feb 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-07290016586763 registered 4 Aug 2026 Active
  • FDA GUDID UDI-DI 07290016586763 listed 2 Feb 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07290016586763
  2. Registered EUDAMED B-07290016586763

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
triLift EUDAMED
triLift FACE GUDID
Generic name
Radio-frequency skin surface treatment system applicator
Device name
triLift 2.0
Model / Ref / Catalog
triLift, 30020100, triLift FACE
Primary DI / UDI-DI
07290016586763
Basic UDI-DI
B-07290016586763
FDA product code
GEI, NGX
EMDN code
Z12040299 General medicine therapeutic treatment instruments - other
GMDN term
Radio-frequency skin surface treatment system applicator
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.4400, 890.5850
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
triLift
30020100
GUDID
triLift FACE
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

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

Similar devices in this category

Other devices filed under GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - OTHER.

Other devices from Pollogen Ltd

See all devices from Pollogen Ltd →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)