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Small Bone Phantom Intramedullary Nail System
FDA UDIClass II (US FDA UDI)
by Paragon 28
Identity
- Trade Name
- Small Bone Phantom Intramedullary Nail System FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- Lapidus Nail, HX10 x 138mm Solid Driver FDA UDI
- Model / Reference
- P99-191-LT10 FDA UDI
- Description
- Lapidus Nail, HX10 x 138mm Solid Driver FDA UDI
Identifiers
- Catalog Number
- P99-191-LT10 FDA UDI
- Primary DI / UDI-DI
- 00889795041302 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 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
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
MR Unsafe FDA UDI
Category: Surgical screwdriver, reusable
Small Bone Phantom Intramedullary Nail System by Paragon 28 — 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
- Paragon 28
Sources (1)
- FDA UDI 9910992f-92f2-4ebe-bdf1-dad38e7d51d8 34 fields · synced Jun 1, 2026