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TASC-II aortoiliac lesion classification of modified class A, B, C, or D;\n3. Rutherford classification score of 2 to 5;\n4. Access site compatibility with the device delivery system;\n5. Compliance with the device's instructions for use (IFU);\n6. Patient availability for appropriate follow-up times for the duration of the study;\n7. Patient informed about the nature of the study, agreeing to its provisions, and signing the informed consent form.\n\nExclusion Criteria:\n\n1. Known hypersensitivity to heparin, contrast media, or stent components;\n2. Patient with blood dyscrasia;\n3. Pregnant or breastfeeding women;\n4. Patient currently participating in an investigational drug or device study;\n5. Patient undergoing chemotherapy or radiation therapy;\n6. Patient with a stent or graft located in the target limb;\n7. Patient who underwent angioplasty or bypass surgery within 30 days prior to inclusion in this study;\n8. Patient with a life expectancy of less than 12 months;\n9. 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