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Divine Pro

EUDAMED

Class IIb (EU MDR)

Ref 35000200BK,35000500Model OptiLiftRef 35000200BK

by Pollogen Ltd

Identity

Device Name
Divine Pro EUDAMED
Model / Reference
OptiLift EUDAMED
35000200BK,35000500 EUDAMED
35000200BK EUDAMED

Identifiers

Primary DI / UDI-DI
07290016586473 EUDAMED
Basic UDI-DI
B-07290016586473 EUDAMED
EMDN Code
Z12040280,Z12040299 EUDAMED
Z12040299 GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - OTHER 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

Divine Pro 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 (3)

  • EUDAMED c3dae215-3601-4b11-b08f-9866fa241f23 61 fields · synced Sep 30, 2026
  • EUDAMED c3dae215-3601-4b11-b08f-9866fa241f23-1 61 fields · synced Jun 10, 2026
  • EUDAMED e4e9d7ce-bd63-4a7b-a920-de8ba66ef6e9 61 fields · synced Sep 30, 2026