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Guidewire Syringe

EUDAMED

Class I (EU MDR)

Ref 251001Model 5mL

by Tianck Medical Co., Ltd.

Identity

Device Name
Guidewire Syringe EUDAMED
Model / Reference
5mL EUDAMED
251001 EUDAMED

Identifiers

Primary DI / UDI-DI
06971162816997 EUDAMED
Basic UDI-DI
B-06971162816997 EUDAMED
EMDN Code
C9080 CARDIOCIRCULATORY SYSTEM DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I 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

Guidewire Syringe by Tianck Medical Co., Ltd. — Class I — 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-000007451
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED be854022-42ea-4cca-bac3-38666e5c5c9f 61 fields · synced Oct 6, 2026