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Single Use Biopsy Forceps

EUDAMED

Class IIa (EU MDR)

Ref BF0218120Model BF0118120

by Suzhou Lantex Medical Technology Company Limited

Identity

Device Name
Single Use Biopsy Forceps EUDAMED
Model / Reference
BF0118120 EUDAMED
BF0218120 EUDAMED

Identifiers

Primary DI / UDI-DI
06971062272961 EUDAMED
Basic UDI-DI
697106227BFWD EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

Single Use Biopsy Forceps by Suzhou Lantex Medical Technology Company Limited — 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-000039444
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 2d10d3bb-03b7-411a-bd4e-8d1a9dad680a 61 fields · synced Jun 19, 2026