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GORE® TAG® Conformable Thoracic Stent Graft with ACTIVE CONTROL System - 

Straight Devices

Catalogue NumberProximal  Diameter (mm)Distal  Diameter (mm)Endoprosthesis Length (cm)
TGM212110E 212110
TGM262610E 262610
TGM282810E 282810
TGM282815E 282815
TGMR313110E 313110
TGMR313115E 313115
TGMR313120E 313120
TGM343410E 343410
TGM343415E 343415
TGM343420E 343420
TGMR373710E 373710
TGMR373715E 373715
TGMR373720E 373720
TGMR404010E 404010
TGMR404015E 404015
TGMR404020E 404020
TGM454510E 454510
TGM454515E 454515
TGM454520E 454520

GORE® TAG® Conformable Thoracic Stent Graft with ACTIVE CONTROL System - 

Tapered Devices

Catalogue NumberProximal  Diameter (mm)Distal  Diameter (mm)Endoprosthesis Length (cm)
TGM262610E 262110
TGMR312610E 312610
TGM342815E342815
TGMR373115E373115
TGMR403415E 403415
TGM453715E453715


Sizing, availability, and pricing varies by country. 

 

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® Conformable Thoracic Stent Graft is indicated for endovascular repair of all lesions of the descending thoracic aorta, including isolated lesions, such as aneurysm and traumatic transection, and Type B dissections.

CONTRAINDICATIONS: The GORE® TAG® Conformable Thoracic Stent Graft is contraindicated in:

  • Patients with known sensitivities or allergies to the device materials  
  • Patients with a systemic infection who may be at risk of endovascular graft infection
Product may not be available in all countries. Please check with your Gore representative for availability.