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Vertebroneedle

EUDAMED

Class IIa (EU MDR)

Ref KMVT1112025C-A

by Biopsybell Srl

Identity

Trade Name
VERTEBRONEEDLE EUDAMED
Device Name
VERTEBROPLASTY SYSTEMS EUDAMED
VERTEBRONEEDLE EUDAMED
Model / Reference
KMVT1112025C-A EUDAMED

Identifiers

Primary DI / UDI-DI
08033860007775 EUDAMED
Basic UDI-DI
8033860VERTFT05CL EUDAMED
B-08033860007775 EUDAMED
EMDN Code
A019011 INTRAOSSEOUS INFUSION AND VERTEBROPLASTY INFUSION 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: Intraosseous infusion kit

Vertebroneedle by Biopsybell Srl — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intraosseous infusion kit.

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 45743b2c-5615-4367-bf21-0456e5089c66 61 fields · synced Jul 9, 2026
  • EUDAMED 4ffa3c80-ca25-4ff9-be0c-a51154d567c1 61 fields · synced May 19, 2026