Identity
- Trade Name
- VERONAIL TITANIUM TROCHANTERIC NAIL FDA UDI
- Generic Name
- Orthopaedic reamer handle FDA UDI
- Device Name
- UNIVERSAL CHUCK WITH T-HANDLE FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- UNIVERSAL CHUCK WITH T-HANDLE FDA UDI
Identifiers
- Catalog Number
- 17955 FDA UDI
- Primary DI / UDI-DI
- 18032937168880 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Orthopaedic reamer handle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic reamer handle
Veronail Titanium Trochanteric Nail by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic reamer handle.
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- MAKO — MAKO Surgical Corp. · Class II
- R3 — Smith & Nephew, Inc. · Class I
- R3 — Smith & Nephew, Inc. · Class I
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 bf419e39-d343-4d2c-a9fa-bea52c2ee9ef 35 fields · synced Jun 7, 2026