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Optimos™ Guidewire

EUDAMED

Class IIa (EU MDR)

Ref GW2-26SModel GW3-45S

by Taewoong Medical Co., Ltd.

Identity

Trade Name
Optimos™ Guidewire EUDAMED
Device Name
Optimos™ Guidewire EUDAMED
Model / Reference
GW3-45S EUDAMED
GW2-26S EUDAMED

Identifiers

Primary DI / UDI-DI
08809293839357 EUDAMED
Basic UDI-DI
880923433-GW-CH EUDAMED
EMDN Code
G0399 DIGESTIVE ENDOSCOPY DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium 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

Optimos™ Guidewire by Taewoong Medical Co., Ltd. — Class IIa — 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

EUDAMED SRN
KR-MF-000007515
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED a3276d6c-00bc-44bf-8bd9-1488cb6fc87f 61 fields · synced May 22, 2026