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Gamma

EUDAMED

Class IIa (EU MDR)

Ref GM2310E

by Biopsybell Srl

Identity

Trade Name
GAMMA EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
Model / Reference
GM2310E EUDAMED

Identifiers

Primary DI / UDI-DI
08033860026172 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

Gamma by Biopsybell Srl — Class IIa — 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

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED f3576188-f3e7-47c2-9cfb-8eb4aa181d22 61 fields · synced Jun 18, 2026