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Abro

EUDAMED

Class IIb (EU MDR)

Ref SWF21VP22F

by Seawon Meditech Co., Ltd.

Identity

Trade Name
ABRO EUDAMED
Device Name
ABRO & Turtle Gun EUDAMED
Model / Reference
SWF21VP22F EUDAMED

Identifiers

Primary DI / UDI-DI
08809272560746 EUDAMED
Basic UDI-DI
B-08809272560746 EUDAMED
EMDN Code
K0201010301 OPEN ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy 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

Category: Open-surgery electrosurgical electrode, monopolar, single-use

Abro by Seawon Meditech Co., Ltd. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical electrode, monopolar, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
KR-MF-000007442
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 61faffc2-a8b5-407d-a664-d41b1a505263 61 fields · synced Jun 18, 2026