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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref 400106004Model 40010001

by Yangzhou Fartley Medical Instrument Technology Co., Ltd.

Identity

Trade Name
Disposable Biopsy Forceps EUDAMED
Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
40010001 EUDAMED
400106004 EUDAMED

Identifiers

Primary DI / UDI-DI
06970900853355 EUDAMED
Basic UDI-DI
69709008510137W EUDAMED
Direct Marketing DI
06970900853355 EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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 Yangzhou Fartley Medical Instrument 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-000009371
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED 4c186561-034a-4313-840a-fd5b730c1ad6 61 fields · synced Jun 19, 2026