Identity
- Trade Name
- Trial 16mm FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- Trial 16mm FDA UDI
- Model / Reference
- FPT2516 FDA UDI
- Description
- Trial 16mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- M739FPT2516 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Spinal implant trial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
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
Trial 16mm by Captiva Spine — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
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Manufacturer
- Manufacturer
- Captiva Spine
Sources (1)
- FDA UDI fb5424df-ccba-4c01-96ed-befb3d7c10f4 34 fields · synced May 30, 2026