The purpose of this registry is to collect safety and performance data on all commercially available Terumo Aortic knitted and woven grafts, and cardiovascular patches in standard clinical practice.
Data will be collected both retrospectively and prospectively.
Patient meets the minimum age as per local regulations at time of consent
Patient requires treatment with study device(s) according to the IFU(s)
Patient is willing and able to comply with all SOC procedures and study visits
Patient or their legally authorised representative (LAR) has given written informed consent to participate in study, including consent to collect data retrospectively
Patient is unable or unwilling to comply with the SOC procedures or follow-up regime
Patient is contraindicated per the device IFU
Patient has any other medical, social or psychological problems that in the opinion of the investigator preclude them from receiving this treatment and the procedures and evaluations pre- and post-procedure