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Shun GS

EUDAMED

Class III (EU MDR)

Ref 626755

by Shunmei Medical Co., Ltd

Identity

Trade Name
Shun GS EUDAMED
Device Name
PTCA Guide Wire EUDAMED
Model / Reference
626755 EUDAMED

Identifiers

Primary DI / UDI-DI
06956014467558 EUDAMED
Basic UDI-DI
B-06956014467558 EUDAMED
EMDN Code
C04010101 CORONARY ARTERY DIAGNOSTIC GUIDEWIRES, HYDROPHILIC EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye 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

Shun GS by Shunmei Medical Co., Ltd — Class III — 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
CN-MF-000001160
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 21ca125a-ca2b-4742-af6a-63fee02a4207 61 fields · synced Sep 18, 2026