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Vertebrosteel

EUDAMED

Class IIa (EU MDR)

Ref KMFVT1310025C-A

by Biopsybell Srl

Identity

Trade Name
VERTEBROSTEEL EUDAMED
Device Name
VERTEBROSTEEL EUDAMED
VERTEBROPLASTY SYSTEMS EUDAMED
Model / Reference
KMFVT1310025C-A EUDAMED

Identifiers

Primary DI / UDI-DI
08033860002176 EUDAMED
Basic UDI-DI
B-08033860002176 EUDAMED
8033860VERTFT05CL 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

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED c065826f-59ca-45bc-ae0a-9e43aa4d6426 61 fields · synced Jul 15, 2026
  • EUDAMED 8cca8102-2160-454a-b332-b99bb11bd512 61 fields · synced May 18, 2026