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Gamma

EUDAMED

Class IIa (EU MDR)

Ref GM1810EC

by Biopsybell Srl

Identity

Trade Name
GAMMA EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
GAMMA EUDAMED
Model / Reference
GM1810EC EUDAMED

Identifiers

Primary DI / UDI-DI
08033860022587 EUDAMED
Basic UDI-DI
8033860BIOEFT01U5 EUDAMED
B-08033860022587 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

Gamma by Biopsybell Srl — Class IIa — MDD, 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/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 6e052e7c-0161-4957-acf5-1ea14c97639b 61 fields · synced Jul 14, 2026
  • EUDAMED 09dbc70c-730b-4cc6-8cb9-bdcd74c99ed0 61 fields · synced May 19, 2026