Identity
- Trade Name
- PNP Tibia FDA UDI
- Generic Name
- Orthopaedic guidewire, single-use FDA UDI
- Device Name
- 3.2mm x 330mm K-Wire, Threaded, 316L FDA UDI
- Model / Reference
- 01-1510-0041-S FDA UDI
- Description
- 3.2mm x 330mm K-Wire, Threaded, 316L FDA UDI
Identifiers
- Catalog Number
- 01-1510-0041-S FDA UDI
- Primary DI / UDI-DI
- 00840194493895 FDA UDI
- FDA Product Code
- KIJ FDA UDI
- GMDN Term
- Orthopaedic guidewire, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthopaedic guidewire, single-use
PNP Tibia by Orthopediatrics Corp. — 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
- Orthopediatrics Corp.
Sources (1)
- FDA UDI 0e966f19-4a4c-47db-8f76-c939105ac090 35 fields · synced Jun 8, 2026