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Zange, verstärkt

EUDAMED

Class IIa (EU MDR)

Ref MP1318

by Shenzhen Edge Medical Co., Ltd.

Identity

Trade Name
Zange, verstärkt EUDAMED
Device Name
Non-Active Forceps EUDAMED
Model / Reference
MP1318 EUDAMED

Identifiers

Primary DI / UDI-DI
06942854300148 EUDAMED
Basic UDI-DI
697507099MF000GV EUDAMED
Direct Marketing DI
06942854300148 EUDAMED
EMDN Code
L1304 ROBOTIC SURGERY FORCEPS AND GRASPERS, REUSABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Zange, verstärkt by Shenzhen Edge Medical 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

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Manufacturer

EUDAMED SRN
CN-MF-000039045
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 495bc506-3bc7-46fc-878c-ef93c3f61b71 61 fields · synced Jul 29, 2026