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Vertebrosteel

EUDAMED

Class IIa (EU MDR)

Ref KMFVT1307025C-A

by Biopsybell Srl

Identity

Trade Name
VERTEBROSTEEL EUDAMED
Device Name
VERTEBROSTEEL EUDAMED
VERTEBROPLASTY SYSTEMS EUDAMED
Model / Reference
KMFVT1307025C-A EUDAMED

Identifiers

Primary DI / UDI-DI
08033860017668 EUDAMED
Basic UDI-DI
B-08033860017668 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 15a1baf2-227f-4438-b3ce-8369ed53ca33 61 fields · synced Sep 18, 2026
  • EUDAMED 433d47d2-8e4c-4939-ae6c-018781a52f7b 61 fields · synced May 19, 2026