Identity
- Trade Name
- LCS FDA UDI
- Generic Name
- Orthopaedic bone calliper FDA UDI
- Device Name
- LCS HIGH PERFORMANCE INSTRUMENTS FEMORAL SIZING CALIPER FDA UDI
- Model / Reference
- 2287-69-000 FDA UDI
- Description
- LCS HIGH PERFORMANCE INSTRUMENTS FEMORAL SIZING CALIPER FDA UDI
Identifiers
- Catalog Number
- 228769000 FDA UDI
- Primary DI / UDI-DI
- 10603295110347 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
- 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
No
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
Category: Orthopaedic bone calliper
Lcs by Depuy Orthopaedics, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Depuy Orthopaedics, Inc.
Sources (1)
- FDA UDI c13cd558-95b3-4ee8-8df9-201d9fc2c42e 35 fields · synced Jun 8, 2026