← Back to catalogue

Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref 1204Model ZRH-BFA-****-CZS ZRH-BFA-****-CZL ZRH-BFA-****-CWS ZRH-BFA-****-CWL ZRH-BFA-****-PZS ZRH-BFA-****-PZL ZRH-BFA-****-PWS ZRH-BFA-****-PWL(1812/,1816,1818,2416,2418,2423)

by Jiangxi ZhuoRuiHua Medical Instrument Co., Ltd.

Identity

Trade Name
Disposable Biopsy Forceps EUDAMED
Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
ZRH-BFA-****-CZS ZRH-BFA-****-CZL ZRH-BFA-****-CWS ZRH-BFA-****-CWL ZRH-BFA-****-PZS ZRH-BFA-****-PZL ZRH-BFA-****-PWS ZRH-BFA-****-PWL(1812/,1816,1818,2416,2418,2423) EUDAMED
1204 EUDAMED

Identifiers

Primary DI / UDI-DI
16972263484419 EUDAMED
Basic UDI-DI
B-16972263484419 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

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: Flexible endoscopic biopsy forceps, single-use

Disposable Biopsy Forceps by Jiangxi ZhuoRuiHua Medical Instrument Co., Ltd. — Class IIa — MDD — 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/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000027760
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED e284cb98-628b-4149-8db4-2589981a1015 61 fields · synced Oct 6, 2026