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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref AG-50110-2318

by Hangzhou AGS MedTech Co., Ltd.

Identity

Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
AG-50110-2318 EUDAMED

Identifiers

Primary DI / UDI-DI
06959664904831 EUDAMED
Basic UDI-DI
6959664950110000127 EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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 Biopsy 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 dd1b70dd-c96d-4545-88bc-0818f7c7b244 61 fields · synced Jun 19, 2026