Identity
- Trade Name
- EAGLE SWIFT FDA UDI
- Generic Name
- Orthopaedic bone calliper FDA UDI
- Device Name
- EAGLE/SWIFT ANTERIOR CERVICAL PLATE SYSTEM CALIPER FDA UDI
- Model / Reference
- 286503000 FDA UDI
- Description
- EAGLE/SWIFT ANTERIOR CERVICAL PLATE SYSTEM CALIPER FDA UDI
Identifiers
- Catalog Number
- 286503000 FDA UDI
- Primary DI / UDI-DI
- 10705034212739 FDA UDI
- FDA Product Code
- KTZ FDA UDI
- GMDN Term
- Orthopaedic bone calliper FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4150 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Eagle Swift by Depuy Spine, Inc. — 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
- Depuy Spine, Inc.
Sources (1)
- FDA UDI f8a9123b-213e-42d7-b8b0-548b24ee8cc7 36 fields · synced Jun 7, 2026