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Forceps

EUDAMED

Class I (EU MDR)

Ref N5173Model /

by Shenyang Shenda Endoscope Co., Ltd.

Identity

Device Name
Forceps EUDAMED
Model / Reference
/ EUDAMED
N5173 EUDAMED

Identifiers

Primary DI / UDI-DI
06971244210798 EUDAMED
Basic UDI-DI
697124421SSQ0002N6 EUDAMED
EMDN Code
L060403 ENDOSCOPIC UROLOGY FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Forceps by Shenyang Shenda Endoscope Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000030478
Authorised Representative
Lepu Medical (Europe) Cooperatief U.A. NL-AR-000000551

Sources (1)

  • EUDAMED b5af6ca5-7597-423d-924a-e3e8ea267ffe 61 fields · synced Jun 19, 2026