← Back to catalogue

Renova Spine Bone Filler

EUDAMED

Class IIa (EU MDR)

Ref RESFIL1515C1CH3

by Biopsybell Srl

Identity

Trade Name
RENOVA SPINE BONE FILLER EUDAMED
Device Name
KYPHOPLASTY SYSTEMS EUDAMED
RENOVA SPINE BONE FILLER EUDAMED
Model / Reference
RESFIL1515C1CH3 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860021443 EUDAMED
Basic UDI-DI
8033860KYPFT05A9T EUDAMED
B-08033860021443 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 — MDD, MDR — 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/MDD

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 9f68b232-a9af-484b-b270-8676d4aba5bb 61 fields · synced Jun 17, 2026
  • EUDAMED 8528dda9-e88c-44e8-869f-013bee120ef3 61 fields · synced Jun 11, 2026