Identity
- Trade Name
- Self-Reinforced Technology FDA UDI
- Generic Name
- Orthopaedic bone pin, bioabsorbable FDA UDI
- Device Name
- 1.5 MM BONE FIXATION KIT, SELF-REINFORCED TECHNOLOGY, Ø1.5 X 25 MM FDA UDI
- Model / Reference
- BXS6225 FDA UDI
- Description
- 1.5 MM BONE FIXATION KIT, SELF-REINFORCED TECHNOLOGY, Ø1.5 X 25 MM FDA UDI
Identifiers
- Catalog Number
- BXS6225 FDA UDI
- Primary DI / UDI-DI
- 10845854017159 FDA UDI
- FDA Product Code
- HWC FDA UDIMAI FDA UDI
- GMDN Term
- Orthopaedic bone pin, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 25 Millimeter FDA UDIOuter Diameter — 1.5 Millimeter FDA UDI
Category: Orthopaedic bone pin, bioabsorbable
Self-Reinforced Technology by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic bone pin, bioabsorbable.
- ActivaNail™ — Bioretec Oy · Class II
- OSSIOfiber™ Hammertoe Fixation Implant — OSSIO LTD · Class II
- OSSIOfiber® Trimmable Fixation Nail System, Cannulated — OSSIO LTD · Class I
- AESCULAP — AESCULAP, INC. · Class II
- ActivaPin™ — Bioretec Oy · Class II
- OSSIOfiber® Trimmable Fixation Nail System — OSSIO LTD · Class I
- REUNITE SCREW SYSTEM — Biomet Orthopedics, Inc. · Class II
- Inion FreedomPin™ — Inion , Ltd. · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI 12bb0f5e-aca0-4167-9610-68ed741d180b 37 fields · synced May 31, 2026