| Catalogue Number | Nominal Thickness (mm) | Nominal Width (cm) | Nominal Length (cm) |
|---|---|---|---|
| 1305010020E | 2 | 5 | 10 |
| 1305015020E | 2 | 5 | 15 |
| 1310015020E | 2 | 10 | 15 |
| 1315020020E | 2 | 15 | 20 |
| 1320030020E | 2 | 20 | 30 |
| 132603402AE | 2 | 26 | 34* |
| 1405010010E | 1 | 5 | 10 |
| 1405015010E | 1 | 5 | 15 |
| 1410015010E | 1 | 10 | 15 |
| 1415020010E | 1 | 15 | 20 |
| 1420030010E | 1 | 20 | 30 |
| 142603401AE | 1 | 26 | 34* |
* Oval
Sizing, availability and pricing varies by country.
Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly
INDICATIONS FOR USE IN EUROPE: The GORE-TEX® Soft Tissue Patch is indicated for use in the reconstruction of diaphragmatic hernias and chest wall soft tissue deficiencies. 1 mm and 2 mm thicknesses are available. For full thickness or segmental wall defects, use of the GORE-TEX® Soft Tissue Patch 2 mm should be considered.
CONTRAINDICATIONS: The GORE-TEX® Soft Tissue Patch is contraindicated for use in:
- Reconstruction of cardiovascular defects.
- Orthopedic defects, as the primary load bearing support for segmental replacement of tendons or ligaments.
- Passive biological membranes such as dura mater, pericardium or peritoneum.
Use of this product in applications other than those indicated has the potential for serious complications, such as aneurysm formation or undesired healing to surrounding tissues.