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Gamma

EUDAMED

Class IIa (EU MDR)

Ref GM2025E

by Biopsybell Srl

Identity

Trade Name
GAMMA EUDAMED
Device Name
GAMMA EUDAMED
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
Model / Reference
GM2025E EUDAMED

Identifiers

Primary DI / UDI-DI
08033860016906 EUDAMED
Basic UDI-DI
B-08033860016906 EUDAMED
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

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

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 8e5dc47c-6e5a-4073-a252-3b38f5a90fe2 61 fields · synced Jul 9, 2026
  • EUDAMED fc738d6a-80f8-4461-8739-3d0738aa6a58 61 fields · synced May 19, 2026