NA
- Primary DI
- 23596010082613
- Brand
- NA
- Company
- Smith & Nephew, Inc.
- Model
- 128054
- Catalog number
- 128054
- Device description
- K-WIRE DIAMOND POINT ROUND END .062 X 12
- Published
- 2015-08-29
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HTY | PIN, FIXATION, SMOOTH |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HTY | Pin, Fixation, Smooth | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 23596010082613 | Package | GS1 | 6 | In Commercial Distribution |
| 03596010082619 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 23596010082613 | 23596010082613 | |
| 03596010082619 | 03596010082619 | 3596010082619 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic bone wire | A wire intended for the fixation of bone fractures that may be implanted or used short-term (e.g., to hold a plate in the correct position during an intervention). It may be used: 1) as a cerclage wire to aid bone fixation; 2) in a loop or figure-of-eight configuration to reattach, e.g., the tip of the elbow (olecranon), tibial tubercle, or greater trochanter; 3) to augment bone screw/plate fixation; or 4) as a Kirschner wire or K-Wire to stiffen (arthrodese) a toe or finger. It is made of metal [e.g., stainless steel, cobalt-chrome (Co-Cr)], and may be malleable or rigid; some types include a nut designed to be attached to the wire to prevent wire migration. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 045483575
- Device count
- 6
- DM exempt
- true
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 03596010479235 | ECHELON | 71342011 | 71342011 | 2015-09-28 |
| 03596010479266 | ECHELON | 71342014 | 71342014 | 2015-09-28 |
| 03596010479273 | ECHELON | 71342015 | 71342015 | 2015-09-28 |
| 03596010479297 | ECHELON | 71342017 | 71342017 | 2015-09-28 |
| 03596010479303 | ECHELON | 71342018 | 71342018 | 2015-09-28 |
| 03596010479310 | ECHELON | 71342019 | 71342019 | 2015-09-28 |
| 03596010479341 | ECHELON | 71343012 | 71343012 | 2015-09-28 |
| 03596010459749 | SYNERGY | 71309109 | 71309109 | 2015-08-30 |
| 03596010459756 | SYNERGY | 71309110 | 71309110 | 2015-08-30 |
| 03596010459787 | SYNERGY | 71309113 | 71309113 | 2015-08-30 |
| 03596010459794 | SYNERGY | 71309114 | 71309114 | 2015-08-30 |
| 03596010459817 | SYNERGY | 71309116 | 71309116 | 2015-08-30 |
| 03596010459831 | SYNERGY | 71309118 | 71309118 | 2015-08-30 |
| 03596010479259 | ECHELON | 71342013 | 71342013 | 2015-09-28 |
| 03596010479280 | ECHELON | 71342016 | 71342016 | 2015-09-28 |
| 03596010479358 | ECHELON | 71343013 | 71343013 | 2015-09-28 |
| 03596010479365 | ECHELON | 71343014 | 71343014 | 2015-09-28 |
| 03596010479389 | ECHELON | 71343016 | 71343016 | 2015-09-28 |
| 03596010479396 | ECHELON | 71343017 | 71343017 | 2015-09-28 |
| 03596010479402 | ECHELON | 71343018 | 71343018 | 2015-09-28 |
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| 07649990202396 | Geomax Reamer Set | Surgical Fusion Technologies GmbH | HTY | 2025-10-01 |
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| 07630037863984 | APTUS | Medartis AG | HTY | 2025-07-31 |
| 07630037864011 | APTUS | Medartis AG | HTY | 2025-04-08 |
| 07630037864264 | APTUS | Medartis AG | HTY | 2025-04-08 |
| 07613327084191 | STEINMANN | Stryker GmbH | HTY | 2025-01-09 |
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