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Vertebroneedle

EUDAMED

Class IIa (EU MDR)

Ref KMVT1310000C-A

by Biopsybell Srl

Identity

Trade Name
VERTEBRONEEDLE EUDAMED
Device Name
VERTEBROPLASTY SYSTEMS EUDAMED
VERTEBRONEEDLE EUDAMED
Model / Reference
KMVT1310000C-A EUDAMED

Identifiers

Primary DI / UDI-DI
08033860027582 EUDAMED
Basic UDI-DI
8033860VERTFT05CL EUDAMED
B-08033860027582 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

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

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 3f6a6dd4-a9f4-49be-b07b-27b848cdca37 61 fields · synced Aug 3, 2026
  • EUDAMED 9e7d608f-7203-4939-9eda-1154a0ccd140 61 fields · synced May 19, 2026