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ZENFluxion

EUDAMED

Class III (EU MDR)

Ref ZY100030010035A

by Zylox-Tonbridge Medical Technology Co., Ltd.

Identity

Trade Name
ZENFluxion EUDAMED
Device Name
Drug-coated PTA Balloon Catheter EUDAMED
Model / Reference
ZY100030010035A EUDAMED

Identifiers

Primary DI / UDI-DI
06974042970840 EUDAMED
Basic UDI-DI
B-06974042970840 EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

ZENFluxion by Zylox-Tonbridge Medical Technology 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-000010626
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 9c1b525e-107d-41d4-bb97-1a245fd361af 61 fields · synced Jun 18, 2026