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Renova Spine Kyphoplasty Tool Kit
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref RES1312004V
Identity
- Trade Name
- RENOVA SPINE KYPHOPLASTY TOOL KIT EUDAMEDBIOPSYBELL SRL FDA UDI
- Generic Name
- Bone access channel kit FDA UDI
- Device Name
- KYPHOPLASTY SYSTEMS EUDAMEDKYPHOPLASTY TOOL KIT FDA UDI
- Model / Reference
- RES1312004V EUDAMEDRENOVA SPINE KYPHOPLASTY TOOL KIT FDA UDI
- Description
- KYPHOPLASTY TOOL KIT FDA UDI
Identifiers
- Catalog Number
- RES1312004V FDA UDI
- Primary DI / UDI-DI
- 08033860039240 EUDAMEDFDA UDI
- Basic UDI-DI
- 8033860KYPFT05A9T EUDAMED
- FDA Product Code
- OCJ FDA UDI
- EMDN Code
- A019011 INTRAOSSEOUS INFUSION AND VERTEBROPLASTY INFUSION NEEDLES AND KITS EUDAMED
- GMDN Term
- Bone access channel kit FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 888.4540 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 — 13 Gauge FDA UDILength — 120 Millimeter FDA UDI
Renova Spine Kyphoplasty Tool Kit by Biopsybell Srl — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8033860KYPFT05A9T | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Biopsybell Srl
- EUDAMED SRN
- IT-MF-000011601
Sources (2)
- EUDAMED ed7861a2-e15d-4546-9313-7be741f0e482 61 fields · synced Jun 17, 2026
- FDA UDI 7d103838-dc7d-4f59-974e-5cbcf44515ec 36 fields · synced May 30, 2026