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Single-Use Video Flexible Ureterorenoscope

EUDAMED

Class IIa (EU MDR)

Ref RP-U-C04S3Model RP-U-C03R9, RP-U-C03S9, RP-U-C03R3, RP-U-C03S3, RP-U-C04R9, RP-U-C04S9, RP-U-C04R3, RP-U-C04S3

by Guangzhou Red Pine Medical Instrument Co., Ltd.

Identity

Device Name
Single-Use Video Flexible Ureterorenoscope EUDAMED
Model / Reference
RP-U-C03R9, RP-U-C03S9, RP-U-C03R3, RP-U-C03S3, RP-U-C04R9, RP-U-C04S9, RP-U-C04R3, RP-U-C04S3 EUDAMED
RP-U-C04S3 EUDAMED

Identifiers

Primary DI / UDI-DI
06972520302077 EUDAMED
Basic UDI-DI
697252030UREF03JA EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES 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 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 3a948431-616f-4d28-b63c-710844436f93 61 fields · synced Oct 5, 2026