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Kyphokit Vertebral Biopsy Needle

EUDAMED

Class IIa (EU MDR)

Ref KK11-FU

by Biopsybell Srl

Identity

Trade Name
KYPHOKIT VERTEBRAL BIOPSY NEEDLE EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
KYPHOKIT VERTEBRAL BIOPSY NEEDLE EUDAMED
Model / Reference
KK11-FU EUDAMED

Identifiers

Primary DI / UDI-DI
08033860033286 EUDAMED
Basic UDI-DI
8033860BIOEFT01U5 EUDAMED
B-08033860033286 EUDAMED
EMDN Code
A01020203 VERTEBRAL AND PARAVERTEBRAL BIOPSY 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

Kyphokit Vertebral Biopsy Needle 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 43d0d5e9-5505-4a5b-8516-6535728eb21e 61 fields · synced Sep 17, 2026
  • EUDAMED 08183ea9-d14e-4d42-a5e1-784a4b975599 61 fields · synced May 17, 2026