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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref FST-FB-18-105-O-P-A1

by Foresight Technology Co., Ltd.

Identity

Trade Name
Disposable Biopsy Forceps EUDAMED
Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
FST-FB-18-105-O-P-A1 EUDAMED

Identifiers

Primary DI / UDI-DI
06957024907492 EUDAMED
Basic UDI-DI
695702493031JC EUDAMED
Direct Marketing DI
06957024907492 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

Category: Flexible endoscopic biopsy forceps, single-use

Disposable Biopsy Forceps by Foresight Technology 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-000009708
Authorised Representative
Creo Medical, S.L.U. ES-AR-000001355

Sources (1)

  • EUDAMED 63bd3bcb-f1b5-4042-bf29-5d816f6fe8ac 61 fields · synced Jun 18, 2026