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Disposable Grasping Forceps

EUDAMED

Class IIa (EU MDR)

Ref AG-5034-1812Model 5031 series~5036series、50310 series

by Hangzhou AGS MedTech Co., Ltd.

Identity

Device Name
Disposable Grasping Forceps EUDAMED
Model / Reference
5031 series~5036series、50310 series EUDAMED
AG-5034-1812 EUDAMED

Identifiers

Primary DI / UDI-DI
06959664906415 EUDAMED
Basic UDI-DI
6959664950310000139 EUDAMED
EMDN Code
G03080102 GASTROINTESTINAL ENDOSCOPY, EXTRACTION FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Disposable Grasping Forceps by Hangzhou AGS MedTech 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-000011718
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 7e511c70-733d-44dc-af89-6a99755e6e9e 61 fields · synced Jun 19, 2026