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ZENFlow

EUDAMED

Class IIa (EU MDR)

Ref ZW130020006018B

by Zylox-Tonbridge Medical Technology Co., Ltd.

Identity

Trade Name
ZENFlow EUDAMED
Device Name
PTA Balloon Catheter EUDAMED
Model / Reference
ZW130020006018B EUDAMED

Identifiers

Primary DI / UDI-DI
06970596422767 EUDAMED
Basic UDI-DI
B-06970596422767 EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

ZENFlow by Zylox-Tonbridge Medical Technology 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

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Manufacturer

EUDAMED SRN
CN-MF-000010626
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 97cf2130-5658-4643-9ead-071b8fb8d2b8 61 fields · synced Jun 19, 2026