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Flexible Ureterorenoscopes

EUDAMED

Class IIa (EU MDR)

Ref US33J-17-USModel US31D-12-US, US31D-12-EU and etc.

by Shanghai Anqing Medical Instrument Co., Ltd

Identity

Device Name
Flexible Ureterorenoscopes EUDAMED
Model / Reference
US31D-12-US, US31D-12-EU and etc. EUDAMED
US33J-17-US EUDAMED

Identifiers

Primary DI / UDI-DI
06970034211687 EUDAMED
Basic UDI-DI
697003421USWW EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Category: Flexible video ureteroscope, single-use

Flexible Ureterorenoscopes by Shanghai Anqing Medical Instrument Co., Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video ureteroscope, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000008487
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED e0f3f0f9-7de9-4d9b-aed6-90b27c70503a 61 fields · synced Jun 20, 2026