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VesTrek™

EUDAMED

Class III (EU MDR)

Ref TT-PTCA-OTW-BR-ENModel VesTrek™ OTW Balloon Catheter Series

by Dongguan TT Medical, Inc.

Identity

Trade Name
VesTrek™ EUDAMED
Device Name
VesTrek™ OTW Coronary Dilatation Balloon Catheters EUDAMED
Model / Reference
VesTrek™ OTW Balloon Catheter Series EUDAMED
TT-PTCA-OTW-BR-EN EUDAMED

Identifiers

Primary DI / UDI-DI
06934184018312 EUDAMED
Basic UDI-DI
069341840OTWLC EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS 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

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

Category: Coronary angioplasty balloon catheter, cutting/scoring

VesTrek™ by Dongguan Tt Medical, Inc. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000039087
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 7d7099a4-197f-46e8-8f9c-d292dc246f97 61 fields · synced Jun 19, 2026