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Kyphokit Bone Filler

EUDAMED

Class IIa (EU MDR)

Ref KK08-FIL6

by Biopsybell Srl

Identity

Trade Name
KYPHOKIT BONE FILLER EUDAMED
Device Name
KYPHOKIT BONE FILLER EUDAMED
KYPHOPLASTY SYSTEMS EUDAMED
Model / Reference
KK08-FIL6 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860035211 EUDAMED
Basic UDI-DI
B-08033860035211 EUDAMED
8033860KYPFT05A9T 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

Category: Intraosseous infusion kit

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

Similar devices

Also classified as Intraosseous infusion kit.

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 29191047-8c1b-4ff4-9422-485d33996d46 61 fields · synced Jul 10, 2026
  • EUDAMED bde2c67c-cf66-483a-a26a-d42c78e54a3a 61 fields · synced May 19, 2026