3.2mm Stabilizing K-wire
- Primary DI
- 00810097800281
- Brand
- 3.2mm Stabilizing K-wire
- Company
- SMV SCIENTIFIC LLC
- Model
- 1252-5103-000
- Catalog number
- 1252-5103-000
- Device description
- 3.2mm Stabilizing K-wire
- Published
- 2022-02-17
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Product Codes
| Code | Name |
|---|
| FZX | Guide, Surgical, Instrument |
| GFC | Driver, Surgical, Pin |
| OUR | Sacroiliac Joint Fixation |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| FZX | Guide, Surgical, Instrument | General, Plastic Surgery | 1 |
| GFC | Driver, Surgical, Pin | General, Plastic Surgery | 1 |
| OUR | Sacroiliac Joint Fixation | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00810097800281 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00810097800281 | 00810097800281 | 810097800281 | 0810097800281 |
GMDN Terms
| Term | Definition |
|---|
| Surgical drill guide, reusable | A manual surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue (e.g., bone); some types are also intended for guiding bone-coring instruments (e.g., keel punch). It is designed in a tubular form or with guiding holes and may have serrations at its distal end to enable firm placement on hard tissue surfaces (it is not bored into the tissue); it can have a handle or be held by another device (e.g., orthopaedic jig), and typically allows protection of the surrounding soft tissue during surgery. It is typically made of metal and may have graduations along its length; it is not custom-made for a specific patient. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|
| Outer Diameter | 3.2 | Millimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 089645059
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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