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Disposable Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref VTL/BFO2-18-120-R

by Jiangsu Ate Medical Technology Co., Ltd.

Identity

Device Name
Disposable Biopsy Forceps EUDAMED
Model / Reference
VTL/BFO2-18-120-R EUDAMED

Identifiers

Primary DI / UDI-DI
06937023078607 EUDAMED
Basic UDI-DI
69370230QYQ-CST EUDAMED
Direct Marketing DI
06937023078607 EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Disposable Biopsy Forceps by Jiangsu Ate Medical 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-000012853
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 6da261bd-c640-4d78-bea2-b412bbaeac5e 61 fields · synced Aug 2, 2026