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Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref HQ-2.3×1600-W-OModel HQ2.3

by Jiangsu BANA Medical Technology Co., Ltd.

Identity

Device Name
Biopsy Forceps EUDAMED
Model / Reference
HQ2.3 EUDAMED
HQ-2.3×1600-W-O EUDAMED

Identifiers

Primary DI / UDI-DI
06941173336487 EUDAMED
Basic UDI-DI
B-06941173336487 EUDAMED
EMDN Code
K01020104 MINIMALLY INVASIVE SURGERY 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

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

Biopsy Forceps by Jiangsu BANA Medical Technology Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000025963
Authorised Representative
Caretechion GmbH DE-AR-000005946

Sources (1)

  • EUDAMED 5cda3d7d-0e86-492a-ae0c-1c69d8aabaf7 61 fields · synced Jun 18, 2026