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Single-use Urinary Guide Wire

EUDAMED

Class IIa (EU MDR)

Ref UW-S3515

by Anrei Medical (HZ) Co., Ltd.

Identity

Trade Name
Single-use Urinary Guide Wire EUDAMED
Device Name
Single-use Urinary Guide Wire EUDAMED
Model / Reference
UW-S3515 EUDAMED

Identifiers

Primary DI / UDI-DI
06926839811973 EUDAMED
Basic UDI-DI
694831892a008MK EUDAMED
Direct Marketing DI
06926839811973 EUDAMED
EMDN Code
U0601 UROLOGICAL GUIDEWIRES, HYDROPHILIC EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Single-use Urinary Guide Wire by Anrei Medical (HZ) 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

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Manufacturer

EUDAMED SRN
CN-MF-000009964
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED e84b9f9d-4896-4826-bf60-972a76016ba8 61 fields · synced Jun 19, 2026