Identity
- Trade Name
- LCP FDA UDI
- Generic Name
- Surgical instrument/implant rack FDA UDI
- Device Name
- 3.5MM LCP TIBIAL PLATEAU INSTR AND IMPLANT SET GRAPHIC CASE FDA UDI
- Model / Reference
- 60.120.704 FDA UDI
- Description
- 3.5MM LCP TIBIAL PLATEAU INSTR AND IMPLANT SET GRAPHIC CASE FDA UDI
Identifiers
- Catalog Number
- 60120704 FDA UDI
- Primary DI / UDI-DI
- 10886982247766 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Surgical instrument/implant rack FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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: Surgical instrument/implant rack
Lcp by Synthes — 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
- Synthes
Sources (1)
- FDA UDI 41adc8a6-60c4-4f28-8d7c-47321d9d88ea 35 fields · synced May 30, 2026