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Biopsy forceps

EUDAMED

Class IIa (EU MDR)

Ref BP-40119Model 40010001

by Yangzhou Fartley Medical Instrument Technology Co., Ltd.

Identity

Trade Name
Biopsy forceps EUDAMED
Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
40010001 EUDAMED
BP-40119 EUDAMED

Identifiers

Primary DI / UDI-DI
06936603208144 EUDAMED
Basic UDI-DI
69709008510137W EUDAMED
Direct Marketing DI
06936603208144 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

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 42f363a6-ca8f-462b-b1c0-ca56e23e244e 61 fields · synced Jun 19, 2026