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Legend Pro Plus, triLift

EUDAMED

Class IIb (EU MDR)

Ref 30020000, 30020000BKModel triLift

by Pollogen Ltd

Identity

Device Name
Legend Pro Plus, triLift EUDAMED
Model / Reference
triLift EUDAMED
30020000, 30020000BK EUDAMED

Identifiers

Primary DI / UDI-DI
07290016586183 EUDAMED
Basic UDI-DI
B-07290016586183 EUDAMED
EMDN Code
Z12040280,Z12040299 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Legend Pro Plus, triLift by Pollogen Ltd — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Pollogen Ltd
EUDAMED SRN
IL-MF-000031034
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 4d7eca9f-76ed-4f86-b8fc-9ce6af4bbc8d 61 fields · synced Jul 9, 2026
  • EUDAMED 4d7eca9f-76ed-4f86-b8fc-9ce6af4bbc8d-1 61 fields · synced Jun 10, 2026