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Renova Spine Bone Filler

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref RESFIL1114C1DTB

by Biopsybell Srl

Identity

Trade Name
RENOVA SPINE BONE FILLER EUDAMED
BIOPSYBELL FDA UDI
Generic Name
Vertebral body cement cannula FDA UDI
Device Name
KYPHOPLASTY SYSTEMS EUDAMED
RENOVA SPINE BONE FILLER EUDAMED
KYPHOPLASTY BONE FILLER KIT FDA UDI
Model / Reference
RESFIL1114C1DTB EUDAMED
RENOVA SPINE BONE FILLER FDA UDI
Description
KYPHOPLASTY BONE FILLER KIT FDA UDI

Identifiers

Catalog Number
RESFIL1114C1DTB FDA UDI
Primary DI / UDI-DI
08033860024550 EUDAMEDFDA UDI
Basic UDI-DI
8033860KYPFT05A9T EUDAMED
B-08033860024550 EUDAMED
FDA Product Code
OAR FDA UDI
EMDN Code
A019011 INTRAOSSEOUS INFUSION AND VERTEBROPLASTY INFUSION NEEDLES AND KITS EUDAMED
GMDN Term
Vertebral body cement cannula FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4200 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 11 Gauge FDA UDI
Length — 207 Millimeter FDA UDI

Category: Intraosseous infusion kit

Renova Spine Bone Filler by Biopsybell Srl — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraosseous infusion kit.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (3)

  • EUDAMED d4747146-ae2e-4552-9e30-00acd8c71601 61 fields · synced Jul 30, 2026
  • EUDAMED 28cfc09d-2af1-48e9-bef5-3ac91a8b3be7 61 fields · synced May 19, 2026
  • FDA UDI 037c4d09-7af4-4d56-8aed-2c7f26bad52a 36 fields · synced May 27, 2026