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Renova Spine Bone Filler

EUDAMED

Class IIa (EU MDR)

Ref RESFIL0812C3

by Biopsybell Srl

Identity

Trade Name
RENOVA SPINE BONE FILLER EUDAMED
Device Name
RENOVA SPINE BONE FILLER EUDAMED
KYPHOPLASTY SYSTEMS EUDAMED
Model / Reference
RESFIL0812C3 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860018849 EUDAMED
Basic UDI-DI
B-08033860018849 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 8617c9bd-2fab-4b5a-8f1f-99d1dececdaa 61 fields · synced Aug 4, 2026
  • EUDAMED 80fb9496-5c0c-4e87-b897-5cebd8da396c 61 fields · synced May 19, 2026