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Octopus RF electrode

EUDAMED

Class IIb (EU MDR)

Ref 17-20P3040_V2-Duo

by STARmed Co., Ltd.

Identity

Trade Name
Octopus RF electrode EUDAMED
Device Name
Octopus RF electrode EUDAMED
Model / Reference
17-20P3040_V2-Duo EUDAMED

Identifiers

Primary DI / UDI-DI
08809306764836 EUDAMED
Basic UDI-DI
880930676Octopus_E9Z EUDAMED
EMDN Code
K0201010301 OPEN ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Octopus RF electrode by Starmed Co., Ltd — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
STARmed Co., Ltd.
EUDAMED SRN
KR-MF-000008605
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED c3b1fa79-774f-4a84-803b-1c533dcefed9 61 fields · synced Jun 18, 2026