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Core Biopsy Puncture Sheath V

EUDAMED

Class IIa (EU MDR)

Ref 170561-US

by Biopsybell Srl

Identity

Trade Name
CORE BIOPSY PUNCTURE SHEATH V EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
Model / Reference
170561-US EUDAMED

Identifiers

Primary DI / UDI-DI
08033860021993 EUDAMED
Basic UDI-DI
8033860BIOEFT01U5 EUDAMED
EMDN Code
A01020102 ASPIRATION FINE NEEDLES AND KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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: Diskectomy system, percutaneous, automatic

Core Biopsy Puncture Sheath V by Biopsybell Srl — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Diskectomy system, percutaneous, automatic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED 476d969c-a925-44a2-b497-759582e3104b 61 fields · synced Jun 19, 2026