← Back to catalogue

Guidewires

EUDAMED

Class IIa (EU MDR)

Ref 155043Model Nitinol 0.025"x45cm(J)

by Tianck Medical Co., Ltd.

Identity

Device Name
Guidewires EUDAMED
Model / Reference
Nitinol 0.025"x45cm(J) EUDAMED
155043 EUDAMED

Identifiers

Primary DI / UDI-DI
06971162812869 EUDAMED
Basic UDI-DI
B-06971162812869 EUDAMED
EMDN Code
C04020102 PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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

Guidewires by Tianck Medical Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000007451
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED b513d64d-b43a-4297-90aa-4812a0e113e9 61 fields · synced Jun 19, 2026