Background: To study the molding method for twenty fetal complex cardiovascular malformation models (CCMM) and its significance in prenatal diagnosis and teaching.Methods: The modified vascular anatomical molding method was used to cast the micro blood vessels and trachea of twenty specimens diagnosed with complex congenital heart disease. Subsequently, twenty abnormal vascular models of the fetal aorta, pulmonary artery and other branches were analyzed and compared with the prenatal ultrasound to summarize their characteristics and misdiagnosis. Results: It was observed that all twenty cases of the fetuses were confirmed with complex cardiac malformations. A total of 69 cardiac malformations were recorded, among which 7 cases were misdiagnosed using prenatal echocardiography (including 3 cases of the interrupted aortic arch (IAA) and 3 cases of double outlet right ventricle (DORV) with transposition of the great arteries (TGA) confirmed by CCMM, case 5.12.14.15.16.17.18), and 18 were missed by prenatal echocardiography (including 5 cases of abnormal ductus arteriosus, 1 case of infrahepatic interruption of the inferior vena cava (IIVC), 1 case of the right aortic arch with mirror-image branching (RAMI), and 3 cases of aberrant subclavian artery (ASA), All cases except 5.8). Conclusion: There are many different kinds of abnormalities in the fetal aorta, pulmonary artery and other branches, which are often complicated with intracardiac malformation and arterial/venous branch variation. Prenatal echocardiography has important diagnostic value; a vascular model can directly show its characteristic changes, which is helpful to improve the differential diagnosis of complex congenital heart disease. Our findings prove that CCMM can play an important role in the clinics, scientific research, teaching, and popular cardiovascular science. Furthermore, it can promote the development of fetal cardiac surgery and the diagnosis with medical imaging and the teaching of medical theory.