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Single Use Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref MD-E-BF2420R

by Zhejiang Chuangxiang Medical Technology Co., LTD.

Identity

Trade Name
Single Use Biopsy Forceps EUDAMED
Device Name
Single Use Biopsy Forceps EUDAMED
Model / Reference
MD-E-BF2420R EUDAMED

Identifiers

Primary DI / UDI-DI
06936534341316 EUDAMED
Basic UDI-DI
69365343BFErespiratoryLL EUDAMED
EMDN Code
R0702010101 BRONCHOSCOPIC SURGERY COLD BIOPTIC 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

Single Use Biopsy Forceps by Zhejiang Chuangxiang Medical 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-000012417
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED a5cfca6f-8648-42a6-bd5d-45b9f84de54b 61 fields · synced May 29, 2026