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Disposable Swinging Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref AG-5021-1823Model 5021 series~50216series

by Hangzhou AGS MedTech Co., Ltd.

Identity

Device Name
Disposable Swinging Biopsy Forceps EUDAMED
Model / Reference
5021 series~50216series EUDAMED
AG-5021-1823 EUDAMED

Identifiers

Primary DI / UDI-DI
06959664900215 EUDAMED
Basic UDI-DI
695966495021000012Q EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY 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

Category: Flexible endoscopic biopsy forceps, single-use

Disposable Swinging Biopsy Forceps by Hangzhou AGS MedTech Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, 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-000011718
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 8c2c90e1-c33c-463f-a7a2-c277aa4aeafc 61 fields · synced Jun 19, 2026