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Anterolateral Distal Tibia Plate, Xl, 27-Hole, Left
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- ANTEROLATERAL DISTAL TIBIA PLATE, XL, 27-HOLE, LEFT FDA UDI
- Generic Name
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
- Model / Reference
- 3035-027 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00848665029130 FDA UDI
- FDA Product Code
- HRS FDA UDI
- GMDN Term
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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 fixation plate, non-bioabsorbable
Anterolateral Distal Tibia Plate, Xl, 27-Hole, Left by Advanced Orthopaedic Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID
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Also classified as Orthopaedic fixation plate, non-bioabsorbable.
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Advanced Orthopaedic Solutions, Inc.
Sources (1)
- FDA UDI 171d5b43-52c0-4c44-91ce-3cccac257752 33 fields · synced Jun 8, 2026