FDA UDI
In Commercial Distribution
🇺🇸 United States
ILIZAROV SYSTEMS
DI: 28033201846890
·
Model: 102101
·
MEDICALPLASTIC SRL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12
Basic Information
- Brand Name
- ILIZAROV SYSTEMS
- Primary DI
- 28033201846890
- Version / Model
- 102101
- Catalog Number
- 102101
- Company Name
- MEDICALPLASTIC SRL
- Labeler DUNS
- 434581062
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 12
- Record Status
- Published
- Publish Date
- 2025-08-20
- Public Version
- 1
- Public Version Date
- 2025-08-28
- Public Version Status
- New
- Public Device Record Key
- 73339abf-1f77-4eb5-b343-bd5f5a952734
Device Description
1,5 MM DIA 300 MM LENGTH ST. STEEL ILIZAROV WIRE CORTICAL, BAYONET POINT
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- Yes
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- Yes
- Sterilization Methods
- Moist Heat or Steam Sterilization
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| JDW | Pin, Fixation, Threaded | Orthopedic | 888.3040 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 32854 | Orthopaedic bone pin, non-bioabsorbable | A thin, implantable rod intended to be used for the stabilization of a bone fracture or bone grafts, or for an osteotomy or arthrodesis (internal and/or external fixation). It is typically drilled into bone and may be smooth or threaded, solid or cannulated, and/or semi-flexible. Also known as a Kirschner-wire (K-wire), it may in addition be intended to assist with the introduction of a surgical instrument and/or implant; it is not intended for implantation into the intramedullary canal (i.e., not a nail). It is made of a non-bioabsorbable material (e.g., stainless steel). Some designs may have a break-off shank and/or be coated to improve long-term fixation. This is a single-use device. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Unit of Use | 08033201841716 | GS1 | ||||
| Primary | 28033201846890 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K994143 | 000 |