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Monopolar J hook probe

EUDAMED

Class IIb (EU MDR)

Ref LM802

by Unimax Medical Systems Inc.

Identity

Device Name
Monopolar J hook probe EUDAMED
Model / Reference
LM802 EUDAMED

Identifiers

Primary DI / UDI-DI
15060289040304 EUDAMED
Basic UDI-DI
B-15060289040304 EUDAMED
EMDN Code
K0201010302 LAPAR AND THORACOSCOPIC ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

Yes

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

Monopolar J hook probe by Unimax Medical Systems Inc. — 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

EUDAMED SRN
TW-MF-000008895
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED cb3338ee-c10e-4605-87ef-e74719aa20ad 61 fields · synced Jun 20, 2026