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Uretero-Renoscope

EUDAMED

Class I (EU MDR)

Ref Y1340D 2HModel SN-I

by Hangzhou Hawk Optical Electronic Instruments Co., Ltd.

Identity

Device Name
Uretero-Renoscope EUDAMED
Model / Reference
SN-I EUDAMED
Y1340D 2H EUDAMED

Identifiers

Primary DI / UDI-DI
06947014624270 EUDAMED
Basic UDI-DI
69470146RJ00278810V9 EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

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: Flexible video ureteroscope, single-use

Uretero-Renoscope by Hangzhou Hawk Optical Electronic Instruments Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video ureteroscope, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000028791
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED d337ddd3-cc68-44f5-b899-1aa2eddf34dd 61 fields · synced Jul 22, 2026