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Gamma

EUDAMED

Class IIa (EU MDR)

Ref GM1915EC

by Biopsybell Srl

Identity

Trade Name
GAMMA EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
GAMMA EUDAMED
Model / Reference
GM1915EC EUDAMED

Identifiers

Primary DI / UDI-DI
08033860012434 EUDAMED
Basic UDI-DI
8033860BIOEFT01U5 EUDAMED
B-08033860012434 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 — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED ebda6058-2dab-42e4-b50c-9e2425536d74 61 fields · synced Aug 2, 2026
  • EUDAMED 42c0f79d-f94c-41d2-8a1a-f1ec518bd2aa 61 fields · synced May 17, 2026