Identity
- Trade Name
- Advansys DLP/MLP FDA UDI
- Generic Name
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
- Device Name
- The Advansys Midfoof Complete set includes Lisfranc plates, Lapidus plates, screws, and instruments used to guide the implants, including K-wire. The Lisfranc Plate consists of an osteosynthesis plate designed to bridge the tarsometatarsal joints. It is available in different sizes and is implanted using the locking system fixation screws and washers. Lisfranc Plates are intended for fractures, fusions, osteotomies and replantation of small bones at the tarsometatarsal joints. The Lapidus Plate consists of an osteosynthesis plate designed to bridge the first tarometatarsal joint. FDA UDI
- Model / Reference
- ADVANMID FDA UDI
- Description
- The Advansys Midfoof Complete set includes Lisfranc plates, Lapidus plates, screws, and instruments used to guide the implants, including K-wire. The Lisfranc Plate consists of an osteosynthesis plate designed to bridge the tarsometatarsal joints. It is available in different sizes and is implanted using the locking system fixation screws and washers. Lisfranc Plates are intended for fractures, fusions, osteotomies and replantation of small bones at the tarsometatarsal joints. The Lapidus Plate consists of an osteosynthesis plate designed to bridge the first tarometatarsal joint. FDA UDI
Identifiers
- Catalog Number
- ADVANMID FDA UDI
- Primary DI / UDI-DI
- 10381780064374 FDA UDI
- FDA Product Code
- HRS FDA UDIHTY FDA UDI
- GMDN Term
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI888.3040 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Advansys DLP/MLP by Newdeal Sas — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Newdeal Sas
Sources (1)
- FDA UDI 5e5dece5-8720-40c6-8dba-c223ef3bf545 37 fields · synced Jun 8, 2026