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Disposable Non-electric Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref VDK-FB-23-160-O-O-A1

by Jiangsu Vedkang Medical Science and Technology Co., Ltd.

Identity

Trade Name
Disposable Non-electric Biopsy Forceps EUDAMED
Device Name
Disposable Non-electric Biopsy Forceps EUDAMED
Model / Reference
VDK-FB-23-160-O-O-A1 EUDAMED

Identifiers

Primary DI / UDI-DI
06970057574202 EUDAMED
Basic UDI-DI
697005757003HA 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 Non-electric Biopsy Forceps by Jiangsu Vedkang Medical Science and Technology Co., Ltd. — Class IIa — MDR — listed in EUDAMED

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-000008462
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED aea91ea5-1ae7-497c-a71d-0bb19ffc82b4 61 fields · synced Jun 19, 2026