Identity
- Trade Name
- JULIET ® INSTRUMENTATION FDA UDI
- Generic Name
- Bone distraction forceps FDA UDI
- Device Name
- SPREADER FDA UDI
- Model / Reference
- LIN-00 00 07-N FDA UDI
- Description
- SPREADER FDA UDI
Identifiers
- Catalog Number
- LIN-00 00 07-N FDA UDI
- Primary DI / UDI-DI
- 07640139343765 FDA UDI
- FDA Product Code
- HWN FDA UDI
- GMDN Term
- Bone distraction forceps 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
Juliet ® Instrumentation by Spineart — 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
- Spineart
Sources (1)
- FDA UDI fcfe8786-c519-4733-ac9d-c34e58f17b26 35 fields · synced Jun 1, 2026