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GORE®  TAG®  Thoracic Branch Endoprosthesis with 8 mm portal
Aortic component and aortic component delivery system 

Catalogue 

Number

Device 

Diameter (mm)

Intended Aortic 

Diameters (mm)

Internal Portal 

Diameter (mm)

Proximal Segment 

Length (mm)

Proximal Covered 

Length (mm)

Partially Uncovered 

Stent 

Length (mm)

Overall Device 

Length (mm)

GORE®  DRYSEAL Flex 

Introducer Sheath 

Size (Fr)

TAC082110E2116-19.58201731020
TAC082610E2619.5-248201641020
TAC082615E   2619.5-248201641520
TAC082810E  2822-268201641022
TAC082815E  2822-268201641522
TAC082820E  2822-268201642022
TAC083115E  3124-298201641522
TAC083120E  3124-298201642022
TAC083415E  3427-328201551524
TAC083420E  3427-328201552024
TAC083715E   3729-348252051524
TAC083720E   3729-348252052024
TAC084015E  4031-378251961526
TAC084020E  4031-378251962026
TAC084515E  4534-4282518.56.51526
TAC084520E  4534-4282518.56.52026

 

GORE®  TAG®  Thoracic Branch Endoprosthesis with 12 mm portal
Aortic component and aortic component delivery system 

Catalogue 

Number

Device 

Diameter (mm)

Intended Aortic 

Diameters (mm)

Internal Portal 

Diameter (mm)

Proximal Segment 

Length (mm)

Proximal Covered 

Length (mm)

Partially Uncovered 

Stent 

Length (mm)

Overall Device 

Length (cm)

GORE®  DRYSEAL Flex 

Introducer Sheath 

Size (Fr)

TAC123115E   3124-2912403641522
TAC123120E  3124-2912403642022
TAC123415E  3427-3212403551524
TAC123420E  3427-3212403552024
TAC123715E  3729-3412403551524
TAC123720E  3729-3412403552024
TAC124015E  4031-3712403461526
TAC124020E  4031-3712403462026
TAC124515E  4534-42124033.56.51526
TAC124520E  4534-42124033.56.52026

 

GORE®  TAG®  Thoracic Branch Endoprosthesis
Side branch component 

Catalogue 

Number

Device 

Diameter (mm)

Intended Branch 

Vessel 

Diameter (mm)

Portal Segment 

Diameter (mm)

Overall Device 

Length (cm)

Required Branch 

Vessel 

Length (cm)

TSB080806E  86-7.5863
TSB081006E  107.5-9863
TSB081206E  129-11863
TSB081506E  1511-13863
TSB081706E  1713-15863
TSB121506E  1511-131262.5
TSB121706E  1713-151262.5
TSB122006E  2015-181262.5

 

GORE®  TAG®  Thoracic Branch Endoprosthesis
Aortic Extender and Aortic Extender delivery system 

Catalogue 

Number

Device 

Diameter (mm)

Intended Aortic 

Diameters (mm)

Overall Device 

Length (cm) 

Partially Uncovered 

Stent 

Length (mm)

GORE®  DRYSEAL Flex 

Introducer Sheath 

Size (Fr)

TE2136E  2116-19.53.6320
TE2638E  2619.5-243.8420
TE2840E  2822-264422
TE3140E  3124-294422
TE3442E  3427-324.2524
TE3742E  3729-344.2524
TE4043E  4031-374.3626
TE4546E  4534-424.66.526


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 market where this product is available. RXOnly

INDICATIONS FOR USE IN EUROPE: The GORE® TAG® Thoracic Branch Endoprosthesis is intended for endovascular repair of all lesions of the descending thoracic aorta (including isolated lesions, such as aneurysm and traumatic transection, and Type B dissections) while maintaining flow into the left subclavian artery, in patients who have appropriate anatomy.

CONTRAINDICATIONS: The GORE® TAG® Thoracic Branch Endoprosthesis is contraindicated in:

  • Patients with known sensitivities or allergies to the device materials [ePTFE (polytetrafluoroethylene), FEP (fluoroethylpropylene), Nitinol (nickel, titanium), Gold, SB Component only - Heparin (CBAS® Heparin Surface)]
  • Patients who have a condition that threatens to infect the graft
  • Patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II 
Product may not be available in all countries. Please check with your Gore representative for availability.