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Disposable Electric Biopsy Forceps

EUDAMED

Class IIb (EU MDR)

Ref FST-FD-23-ORef FST-FD-23-W

by Foresight Technology Co., Ltd.

Identity

Trade Name
Disposable Electric Biopsy Forceps EUDAMED
Device Name
Disposable Electric Biopsy Forceps EUDAMED
Model / Reference
FST-FD-23-O EUDAMED
FST-FD-23-W EUDAMED

Identifiers

Primary DI / UDI-DI
06957024907898 EUDAMED
06957024904835 EUDAMED
Basic UDI-DI
695702493702K8 EUDAMED
695702493701K6 EUDAMED
Direct Marketing DI
06957024907898 EUDAMED
06957024904835 EUDAMED
EMDN Code
G0308010102 GASTROINTESTINAL ENDOSCOPY, HOT BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain 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 Electric Biopsy Forceps by Foresight Technology Co., Ltd. — Class IIb — 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 (2)

  • EUDAMED 34301994-1a7d-4132-bc39-3f968de3854e 61 fields · synced Sep 18, 2026
  • EUDAMED 6000aefa-5bb8-4e9a-8385-a12f820ff855 61 fields · synced May 18, 2026