← Back to catalogue

Single-Use Video Hysteroscope

EUDAMED

Class IIa (EU MDR)

Ref RP-G-C0101BModel RP-G-C24, RP-G-C0101, RP-G-C0101B

by Guangzhou Red Pine Medical Instrument Co., Ltd.

Identity

Device Name
Single-Use Video Hysteroscope EUDAMED
Model / Reference
RP-G-C24, RP-G-C0101, RP-G-C0101B EUDAMED
RP-G-C0101B EUDAMED

Identifiers

Primary DI / UDI-DI
06972520302138 EUDAMED
Basic UDI-DI
697252030HYSR01L8 EUDAMED
EMDN Code
Z12020704 HYSTEROSCOPES 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 Hysteroscope by Guangzhou Red Pine Medical Instrument 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

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

Manufacturer

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

Sources (1)

  • EUDAMED 7840e243-f520-4e1e-9b32-9ca9de7b53d2 61 fields · synced Oct 7, 2026