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V-Disk

EUDAMED

Class IIa (EU MDR)

Ref 1716PDDCD

by Biopsybell Srl

Identity

Trade Name
V-DISK EUDAMED
Device Name
DISCECTOMY SYSTEMS EUDAMED
Model / Reference
1716PDDCD EUDAMED

Identifiers

Primary DI / UDI-DI
08033860039622 EUDAMED
Basic UDI-DI
8033860DISCFT01D77 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

V-Disk by Biopsybell Srl — Class IIa — 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/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED e92240fb-7caf-4de0-9d04-9b0bc1d3c92f 61 fields · synced Jul 23, 2026