← Back to catalogue

Single-Use Video Flexible Cysto-Nephroscope

EUDAMED

Class IIa (EU MDR)

Ref RP-U-C01ESModel RP-U-C01F, RP-U-C01FS

by Guangzhou Red Pine Medical Instrument Co., Ltd.

Identity

Trade Name
Single-Use Video Flexible Cysto-Nephroscope EUDAMED
Device Name
Single-Use Video Flexible Cysto-Nephroscope EUDAMED
Model / Reference
RP-U-C01F, RP-U-C01FS EUDAMED
RP-U-C01ES EUDAMED

Identifiers

Primary DI / UDI-DI
06972520303005 EUDAMED
Basic UDI-DI
697252030CYSF02GD EUDAMED
Direct Marketing DI
06972520303005 EUDAMED
EMDN Code
Z12020705 NEPHROSCOPES 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 Video Flexible Cysto-Nephroscope 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Guangzhou Red Pine Medical Instrument Co., Ltd.
EUDAMED SRN
CN-MF-000012833
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 8eb07a10-18f8-4071-a066-d4f8c0ed33c8 61 fields · synced Jun 18, 2026