Identity
- Trade Name
- JULIET INSTRUMENTATION FDA UDI
- Generic Name
- Spinal implant trial FDA UDI
- Device Name
- Lateral Trial, 17mm,H12 FDA UDI
- Model / Reference
- JUL-IN 07 17-N FDA UDI
- Description
- Lateral Trial, 17mm,H12 FDA UDI
Identifiers
- Catalog Number
- JUL-IN 07 17-N FDA UDI
- Primary DI / UDI-DI
- 07640151110772 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Spinal implant trial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 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
No
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
Juliet Instrumentation by Spineart — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Spineart
Sources (1)
- FDA UDI 2f675d97-49f6-4ded-ab43-bc294df30fca 35 fields · synced May 31, 2026