Peripheral Vascular Guide Wire

by Tianjin Demax Medical Technology Co., Ltd. 2 variants

Ref DVGW14S182S

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697410893DVGWSSUH Basic UDI-DI 06974108939408UDI-DI	Date14 Sep 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Peripheral Vascular Guide Wire
Model / Reference: DVGW14S182S

Primary DI / UDI-DI: 06974108939408
Basic UDI-DI: 697410893DVGWSSUH
EMDN Code: C04020101 Peripheral vascular diagnostic guidewires, hydrophilic

Device Class: Class IIa
EU market of registration: Romania

Manufacturer details

EUDAMED SRN: CN-MF-000038936
Authorised representative: Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Tianjin Demax Medical Technology Co., Ltd.

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Peripheral Vascular Guide Wire

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Guiding Sheath

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Guiding Sheath

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Guiding Sheath

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Guiding Sheath

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See all devices from Tianjin Demax Medical Technology Co., Ltd. →

Properties

Sterile

Other properties (12)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No