← Back to catalogue

Biopsy forceps, Biopsiezange

EUDAMED

Class I (EU MDR)

Ref 302-605

by ELCON Medical Instruments GmbH

Identity

Device Name
Biopsy forceps, Biopsiezange EUDAMED
Model / Reference
302-605 EUDAMED

Identifiers

Primary DI / UDI-DI
04049113073484 EUDAMED
Basic UDI-DI
404911315001R002001001T8 EUDAMED
Direct Marketing DI
04049113073484 EUDAMED
EMDN Code
L05090301 GYNECOLOGICAL BIOPSY FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Biopsy forceps, Biopsiezange by ELCON Medical Instruments GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

EUDAMED SRN
DE-MF-000005908

Sources (1)

  • EUDAMED ecd694c7-fd54-4e3e-8f48-82bdee525dcb 61 fields · synced Jul 8, 2026