Identity
- Trade Name
- Axis Spine Technologies ALIF System Instrument FDA UDI
- Generic Name
- Bone graft funnel FDA UDI
- Device Name
- GRAFT SYRINGE PLUNGER - MEDIUM FDA UDI
- Model / Reference
- AI-6012.2 FDA UDI
- Description
- GRAFT SYRINGE PLUNGER - MEDIUM FDA UDI
Identifiers
- Catalog Number
- AI-6012.2 FDA UDI
- Primary DI / UDI-DI
- 05056619801793 FDA UDI
- FDA Product Code
- OVD FDA UDI
- GMDN Term
- Bone graft funnel FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone graft funnel
Axis Spine Technologies ALIF System Instrument by Axis Spine Technologies Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Axis Spine Technologies Ltd
Sources (1)
- FDA UDI b2579fa0-a24a-4d6d-ae2a-820f21fbfa20 35 fields · synced May 30, 2026