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Vertebrosteel

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref KMFVT1112000C-A

by Biopsybell Srl

Identity

Trade Name
VERTEBROSTEEL EUDAMED
BIOPSYBELL FDA UDI
Generic Name
Orthopaedic cement preparation/delivery kit FDA UDI
Device Name
VERTEBROPLASTY SYSTEMS EUDAMED
VERTEBROSTEEL EUDAMED
Kyphoplasty/Vertebroplasty system FDA UDI
Model / Reference
KMFVT1112000C-A EUDAMED
VERTEBROSTEEL FDA UDI
Description
Kyphoplasty/Vertebroplasty system FDA UDI

Identifiers

Catalog Number
KMFVT1112000C-A FDA UDI
Primary DI / UDI-DI
08033860015435 EUDAMEDFDA UDI
Basic UDI-DI
8033860VERTFT05CL EUDAMED
B-08033860015435 EUDAMED
FDA Product Code
OAR FDA UDI
EMDN Code
A019011 INTRAOSSEOUS INFUSION AND VERTEBROPLASTY INFUSION NEEDLES AND KITS EUDAMED
GMDN Term
Orthopaedic cement preparation/delivery kit FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4200 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 11 Gauge FDA UDI

Category: Intraosseous infusion kit

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

Similar devices

Also classified as Intraosseous infusion kit.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (3)

  • EUDAMED 564fe8a3-b590-4b55-ab27-5293ff608caa 61 fields · synced Jun 19, 2026
  • EUDAMED efe982cb-8457-43e0-90fc-37e5964ee47c 61 fields · synced May 18, 2026
  • FDA UDI de05fd8e-3b10-403e-87c7-f78ee4bd298e 36 fields · synced May 30, 2026