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Video Ureterorenoscope

EUDAMED

Class IIa (EU MDR)

Ref DR025670B IModel DPG-V

by Hangzhou Hawk Optical Electronic Instruments Co., Ltd.

Identity

Device Name
Video Ureterorenoscope EUDAMED
Model / Reference
DPG-V EUDAMED
DR025670B I EUDAMED

Identifiers

Primary DI / UDI-DI
06947014620326 EUDAMED
Basic UDI-DI
69470146EJ00287410GY EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Video Ureterorenoscope by Hangzhou Hawk Optical Electronic Instruments Co., Ltd. — Class IIa — 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 4bfaa66f-c0a4-40f4-8cd0-c3e7e4e115f2 61 fields · synced Jul 31, 2026