Identity
- Trade Name
- ARIA FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- TRIAL, LORDOSIS FDA UDI
- Model / Reference
- 48759308 FDA UDI
- Description
- TRIAL, LORDOSIS FDA UDI
Identifiers
- Catalog Number
- 48759308 FDA UDI
- Primary DI / UDI-DI
- 07613327272352 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 60.0 Millimeter FDA UDIWidth — 18.0 Millimeter FDA UDIAngle — 8.0 degree FDA UDIHeight — 8.0 Millimeter FDA UDI
Aria by Stryker Corp. — 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
- Stryker Corp.
Sources (1)
- FDA UDI efe0cb53-08a8-4dc8-86d1-9d6189ae7094 36 fields · synced May 31, 2026