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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref EN ISO 13485:2016Model KLF-AΦ2.3×1000-BS

by Hangzhou Kangsheng Medical Equipment Co., Ltd

Identity

Trade Name
Disposable Biopsy Forceps EUDAMED
Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
KLF-AΦ2.3×1000-BS EUDAMED
EN ISO 13485:2016 EUDAMED

Identifiers

Primary DI / UDI-DI
16942599807084 EUDAMED
Basic UDI-DI
B-16942599807084 EUDAMED
EMDN Code
L03130402 FORCEPS FOR EXTERNAL BODIES, REUSABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Bronchoscopic biopsy curette, rigid

Disposable Biopsy Forceps by Hangzhou Kangsheng Medical Equipment Co., Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Bronchoscopic biopsy curette, rigid.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000049095
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 29bbe025-10ce-46ef-b52d-0bfae3d9ccf8 61 fields · synced Jun 19, 2026