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Renova Spine Bone Filler

EUDAMED

Class IIa (EU MDR)

Ref RESFIL1312C1

by Biopsybell Srl

Identity

Trade Name
RENOVA SPINE BONE FILLER EUDAMED
Device Name
RENOVA SPINE BONE FILLER EUDAMED
KYPHOPLASTY SYSTEMS EUDAMED
Model / Reference
RESFIL1312C1 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860030360 EUDAMED
Basic UDI-DI
B-08033860030360 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

Renova Spine 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 7e70c53c-4b44-4bfe-ab2d-d807863ce825 61 fields · synced Jul 20, 2026
  • EUDAMED 171b55b1-99bd-4abd-a7a7-5c522a21354a 61 fields · synced May 19, 2026