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GORE® SYNECOR Biomaterial is not authorized for use in Canada.

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 available8 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 available18 mm trocar incision 
GKWR3040 30 cm x 40 cm Now available18 mm trocar incision 
GKWR3535 35 cm x 35 cm Now available21 mm trocar incision 
GKWR4040 40 cm x 40 cm  Now available24 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.

IFU Consult instructions

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.