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Single-Use Video Flexible Ureterorenoscope

EUDAMED

Class IIa (EU MDR)

Ref RP-U-C0306FModel RP-U-C0306F, RP-U-C0307F, RP-U-C0306FS9, RP-U-C0307FS9

by Guangzhou Red Pine Medical Instrument Co., Ltd.

Identity

Trade Name
Single-Use Video Flexible Ureterorenoscope EUDAMED
Device Name
Single-Use Video Flexible Ureterorenoscope EUDAMED
Model / Reference
RP-U-C0306F, RP-U-C0307F, RP-U-C0306FS9, RP-U-C0307FS9 EUDAMED
RP-U-C0306F EUDAMED

Identifiers

Primary DI / UDI-DI
06972520300509 EUDAMED
Basic UDI-DI
697252030UREF02J8 EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa 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 Video Flexible Ureterorenoscope by Guangzhou Red Pine Medical Instrument Co., Ltd. — Class IIa — MDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000012833
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED fd230aec-463d-41d4-9200-761755413ce7 61 fields · synced May 23, 2026