Catalogue numbers for Conformable GORE® TAG® Thoracic Endoprosthesis

Conformable GORE^® TAG^® Thoracic Endoprosthesis
Catalogue Number	Proximal Diameter (mm)	Distal Diameter (mm)	Endoprosthesis Length (cm)
TGU212110	21	21	10
TGU262110	26	21	10
TGU262610	26	26	10
TGU282810	28	28	10
TGU282815	28	28	15
TGU312610	31	26	10
TGU313110	31	31	10
TGU313115	31	31	15
TGU343410	34	34	10
TGU343415	34	34	15
TGU343420	34	34	20
TGU373710	37	37	10
TGU373715	37	37	15
TGU373720	37	37	20
TGU404010	40	40	10
TGU404015	40	40	15
TGU404020	40	40	20
TGU454510	45	45	10
TGU454515	45	45	15
TGU454520	45	45	20

Sizing, availability, and pricing varies by country.

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. R_XOnly

INDICATIONS FOR USE IN THE U.S.: The GORE^® TAG^® Thoracic Endoprosthesis 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: The GORE^® TAG^® Thoracic Endoprosthesis is contraindicated in: Patients with known sensitivities or allergies to the device materials (Table 1); Patients who have a condition that threatens to infect the graft.