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D-Pack

EUDAMED

Class IIa (EU MDR)

Ref D-PA1716CDRef D-PA1908CD

by Biopsybell Srl

Identity

Trade Name
D-PACK EUDAMED
Device Name
DISCECTOMY SYSTEMS EUDAMED
Model / Reference
D-PA1716CD EUDAMED
D-PA1908CD EUDAMED

Identifiers

Primary DI / UDI-DI
08033860036812 EUDAMED
08033860045715 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

D-Pack 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 (2)

  • EUDAMED 6e052cbb-e89b-4650-9a4f-9e24d31bb301 61 fields · synced Jul 24, 2026
  • EUDAMED 1942a896-d7cf-418c-85a6-792d9cfc6d6b 61 fields · synced May 17, 2026