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Centronail Titanium Universal Femoral Nailing System
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Centronail Titanium Universal Femoral Nailing System FDA UDI
- Generic Name
- Fluted surgical drill bit, single-use, non-sterile FDA UDI
- Device Name
- CANNULATED DRILL D. 6 MM FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- CANNULATED DRILL D. 6 MM FDA UDI
Identifiers
- Catalog Number
- 173285 FDA UDI
- Primary DI / UDI-DI
- 18032937167876 FDA UDI
- FDA Product Code
- JDS FDA UDI
- GMDN Term
- Fluted surgical drill bit, single-use, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 6 Millimeter FDA UDI
Category: Fluted surgical drill bit, single-use, non-sterile
Centronail Titanium Universal Femoral Nailing System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Fluted surgical drill bit, single-use, non-sterile.
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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
- Orthofix, Inc.
Sources (1)
- FDA UDI c1208202-7775-4ec7-83f3-b36c5b1df1aa 36 fields · synced May 30, 2026