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Single-use Flexible Video Ureterorenoscope

EUDAMED

Class IIa (EU MDR)

Ref DURS1-121PRSModel DURS1-121P, DURS1-121PR,DURS1-121PS,DURS1-121PRS,DURS1-120P,DURS1-120PR,DURS1-120PS,DURS1-120PRS

by Himaging Technology (Shanghai) Co., Ltd.

Identity

Trade Name
Single-use Flexible Video Ureterorenoscope EUDAMED
Device Name
Single-use Flexible Video Ureterorenoscope EUDAMED
Model / Reference
DURS1-121P, DURS1-121PR,DURS1-121PS,DURS1-121PRS,DURS1-120P,DURS1-120PR,DURS1-120PS,DURS1-120PRS EUDAMED
DURS1-121PRS EUDAMED

Identifiers

Primary DI / UDI-DI
06974235401120 EUDAMED
Basic UDI-DI
697423540DURSN4 EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium 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 Flexible Video Ureterorenoscope by Himaging Technology (Shanghai) 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-000028002
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 333bf71f-3709-420a-b001-1bc92203743d 61 fields · synced Jun 19, 2026