Identity
- Trade Name
- LCP FDA UDI
- Generic Name
- Orthopaedic implant aiming arm FDA UDI
- Device Name
- SHORT PERIARTICULAR AIMING ARM FOR 4.5MM LCP PROX TIBIA PL-R FDA UDI
- Model / Reference
- SD03.120.001 FDA UDI
- Description
- SHORT PERIARTICULAR AIMING ARM FOR 4.5MM LCP PROX TIBIA PL-R FDA UDI
Identifiers
- Catalog Number
- SD03120001 FDA UDI
- Primary DI / UDI-DI
- 10886982002815 FDA UDI
- FDA Product Code
- FZX FDA UDI
- GMDN Term
- Orthopaedic implant aiming arm FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Lcp by Synthes (u.s.a.) Lp — 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
- Synthes (u.s.a.) Lp
Sources (1)
- FDA UDI 4eadaf1e-38f9-4d1c-a191-2d9c63625ad7 36 fields · synced Jun 1, 2026