← Back to catalogue

Guidewire

EUDAMED

Class IIa (EU MDR)

Ref 155010Model Straight tip, J tip, Angle tip

by Tianck Medical Co., Ltd.

Identity

Device Name
Guidewire EUDAMED
Model / Reference
Straight tip, J tip, Angle tip EUDAMED
155010 EUDAMED

Identifiers

Primary DI / UDI-DI
06971162812630 EUDAMED
Basic UDI-DI
697116281GW15GY EUDAMED
EMDN Code
C04020102 PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-HYDROPHILIC EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Guidewire by Tianck 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

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 d68e2a12-77a9-4888-92ca-320a617f5fad 61 fields · synced Jun 18, 2026