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Paratrooper™ Plantar Plate Repair System
FDA UDIClass II (US FDA UDI)
by Paragon 28
Identity
- Trade Name
- Paratrooper™ Plantar Plate Repair System FDA UDI
- Generic Name
- Suturing unit, single-use FDA UDI
- Device Name
- Paratrooper Plantar Plate Weil Kit, Sterile FDA UDI
- Model / Reference
- P13-000-WEIL-SK FDA UDI
- Description
- Paratrooper Plantar Plate Weil Kit, Sterile FDA UDI
Identifiers
- Catalog Number
- P13-000-WEIL-SK FDA UDI
- Primary DI / UDI-DI
- 00889795103482 FDA UDI
- FDA Product Code
- MBI FDA UDI
- GMDN Term
- Suturing unit, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Suturing unit, single-use
Paratrooper™ Plantar Plate Repair System by Paragon 28 — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Paragon 28
Sources (1)
- FDA UDI a6998331-2a77-4125-a432-3aa1d650faa9 34 fields · synced Jun 1, 2026