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Biopsy Forceps

EUDAMED

Class I (EU MDR)

Ref N&A

by Qureshi Manufacturing Corporation

Identity

Device Name
Biopsy Forceps EUDAMED
Model / Reference
N&A EUDAMED

Identifiers

Primary DI / UDI-DI
111823023271 EUDAMED
Basic UDI-DI
PP12633BIOPSYFORCEPS06 EUDAMED
Direct Marketing DI
111823023271 EUDAMED
EMDN Code
L031301 GENERAL SURGERY BIOPSY FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Bulgaria 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 by Qureshi Manufacturing Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PK-MF-000024744
Authorised Representative
AF Pharma Service Europe SL ES-AR-000018076

Sources (1)

  • EUDAMED 334025e7-ebde-40d6-8c5b-f47e3b391400 61 fields · synced Jul 30, 2026