Identity
- Trade Name
- V-Access FDA UDI
- Generic Name
- Vertebral body cement cannula FDA UDI
- Model / Reference
- VV 15 150 5 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08058964725448 FDA UDI
- FDA Product Code
- OCJ FDA UDI
- GMDN Term
- Vertebral body cement cannula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Category: Vertebral body cement cannula
V-Access by G21 Srl — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- G21 Srl
Sources (2)
- FDA UDI 742d12bc-fdb0-4c05-beec-f900ab715fee 32 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 2, 2026