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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref FST-FB-15-105-W-P

by Foresight Technology Co., Ltd.

Identity

Trade Name
Disposable Biopsy Forceps EUDAMED
Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
FST-FB-15-105-W-P EUDAMED

Identifiers

Primary DI / UDI-DI
06957024911291 EUDAMED
Basic UDI-DI
695702493025JH EUDAMED
Direct Marketing DI
06957024911291 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 Foresight Technology 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-000009708
Authorised Representative
Creo Medical, S.L.U. ES-AR-000001355

Sources (1)

  • EUDAMED 1dd4c685-4497-4487-9bf0-9768a8f7258e 61 fields · synced Jun 18, 2026