GORE® SYNECOR Intraperitoneal Biomaterial | |
|---|---|
| Catalogue Number | Size |
GKFC12 | 12 cm diameter* |
GKFV1015 | 10 cm x 15 cm† |
GKFV1520 | 15 cm x 20 cm† |
GKFR2025 | 20 cm x 25 cm |
GKFR2030 | 20 cm x 30 cm |
Trocar compatibility
GKFR2030 is designed to fit through a 12 mm trocar.
GORE® SYNECOR Preperitoneal Biomaterial | ||
|---|---|---|
| Catalogue Number | MORE SIZE OPTIONS Dimension (cm x cm) | Minimum Recommended Trocar or Trocar Incision Size |
GKWC09 | 9 cm diameter* Now available | 8 mm trocar |
GKWV1015 | 10 cm x 15 cm† | 10 mm trocar |
GKWR1215 | 12 cm x 15 cm | 11 mm trocar |
GKWV1520 | 15 cm x 20 cm† | 12 mm trocar |
GKWR2025 | 20 cm x 25 cm | 15 mm trocar |
GKWR2030 | 20 cm x 30 cm | 15 mm trocar‡ |
GKWR3030 | 30 cm x 30 cm Now available | 18 mm trocar incision |
GKWR3040 | 30 cm x 40 cm Now available | 18 mm trocar incision |
GKWR3535 | 35 cm x 35 cm Now available | 21 mm trocar incision |
GKWR4040 | 40 cm x 40 cm Now available | 24 mm trocar incision |
GKWR4050 | 40 cm x 50 cm Now available | 24 mm trocar incision |
* Circle.
† Oval.
‡ Wetting recommended.
G = Gore
K = Knit
F = Film
W = Web
V = Oval
R = Rectangle
C = Circle
Sizing, availability and pricing varies by country.
Please check with your Gore representative for availability.
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: The GORE® SYNECOR Intraperitoneal Biomaterial device is intended for use in the repair of hernias and abdominal wall or thoracic wall soft tissue deficiencies that may require the addition of a nonabsorbable reinforcing or bridging material.
CONTRAINDICATIONS: The GORE® SYNECOR Intraperitoneal Biomaterial is contraindicated for use in reconstruction of cardiovascular defects.
INDICATIONS FOR USE: The GORE® SYNECOR Preperitoneal Biomaterial device is intended for use in the repair of hernias and abdominal wall soft tissue deficiencies that may require the addition of a non-absorbable reinforcing or bridging material.
CONTRAINDICATIONS: The GORE® SYNECOR Preperitoneal Biomaterial is contraindicated for use in reconstruction of cardiovascular defects.
GORE® SYNECOR Biomaterial is not authorized for use in Canada.