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Diskom

EUDAMED

Class IIa (EU MDR)

Ref DKR1716-SPA

by Biopsybell Srl

Identity

Trade Name
DISKOM EUDAMED
Device Name
DISCECTOMY SYSTEMS EUDAMED
DISKOM EUDAMED
Model / Reference
DKR1716-SPA EUDAMED

Identifiers

Primary DI / UDI-DI
08033860026738 EUDAMED
Basic UDI-DI
8033860DISCFT01D77 EUDAMED
B-08033860026738 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

Diskom 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 b225566b-f15e-4ead-aee8-bf02977a81a9 61 fields · synced Jul 16, 2026
  • EUDAMED 6df06ef7-c472-4f92-822b-df398f65c3ff 61 fields · synced Jun 20, 2026