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Straight devices and Taper devices

Catalogue

Number

Intended 
Aortic

Diameter (mm)

Proximal 
Diameter (mm)
Distal 
Diameter (mm)

Endoprosthesis

Length (cm)

Recommended GORE® DRYSEAL 
Flex Introducer Sheath Size (Fr)
Oversizing 
Range (%)
Partially Uncovered 
Stent Length (mm)
Straight Devices
TGM21211016–19.5212110188–313
TGM26261019.5–24262610208–334
TGM28281022–26282810208–274
TGM28281522–26282815208–274
TGMR31311024–29313110207–294
TGMR31311524–29313115207–294
TGMR31312024–29313120207–294
TGM34341027–32343410226–265
TGM34341527–32343415226–265
TGM34342027–32343420226–265
TGMR37371029–34373710229–285
TGMR37371529–34373715229–285
TGMR37372029–34373720229–285
TGMR40401031–37404010228–296
TGMR40401531–37404015228–296
TGMR40402031–37404020228–296
TGM45451034–42454510247–326.5
TGM45451534–42454515247–326.5
TGM45452034–42454520247–326.5
Taper Devices*
TGM26211019.5-24/16-19.5262110208–334
TGMR31261024-29/19.5-24312610207–334
TGM34281527-32/22-26342815226–275
TGMR37311529-34/24-29373115227–295
TGMR40341531-37/27-32403415226–296
TGM45371534-42/29-34453715247–326.5

* Some sizes not available in all markets.


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 IN THE U.S.: The GORE® TAG® Conformable Thoracic Stent Graft is intended for endovascular repair of all lesions of the descending thoracic aorta, including: isolated lesions in patients who have appropriate anatomy, including: adequate iliac/femoral access, aortic inner diameter in the range of 16-42 mm, ≥ 20 mm non-aneurysmal aorta proximal and distal to the lesion; Type B dissections in patients who have appropriate anatomy, including: adequate iliac/femoral access, ≥ 20 mm landing zone proximal to the primary entry tear; proximal extent of the landing zone must not be dissected, diameter at proximal extent of proximal landing zone in the range of 16-42 mm.

CONTRAINDICATIONS: Patients with known sensitivities or allergies to the device materials; patients who have a condition that threatens to infect the graft.