The inventive arrangement comprises a metallic stent (3), as a medical implant for the treatment of lesions in blood vessels, and a package (1), having an internal volume, is arranged in which the stent (3) protected. The stent (3) has a plurality of lands (33), which together form a tubular shape, and a proximal end (31) and a distal end (32), between which extends a stent lumen (34). The stent surface (35) has a hydrophilic property. Imports coming from the atmosphere molecular chemical contaminants, primarily hydrocarbon compounds are significantly reduced on the surface by a treatment, whereby the contact angle decreased as a measure of the hydrophilicity of the surface (35) seated water droplet relative to the contact angle before this treatment. The stent (3) is stored in an inert in the package (1). The treatment of the surface (35) to reduce the chemical contamination has occurred as a material removal or by material removal. In an extended configuration of the arrangement, a catheter (5) is arranged in the package (1) on which a stent (3) is mounted. The packaging (1) consists of a container (12) with a bottom (10) and a cover (11), of which at least one can be removed or at least an openable access (110), so that the stent (3) or on a catheter (5) mounted stent (3) together with the catheter (5) from the package (1) can be removed. Still further rounds can be integrated into the package (1), a crimping device (4).Mevcut buluş kan damarlarındaki lezyonları tedavi etmek üzere tıbbi implant olarak metal bir stentten ve bir ambalajdan oluşan bir düzeneğe ilişkindir. Stent ambalajın iç hacmi içinde korunaklı şekilde yer alır. Stent, birlikte bir tüp biçimi oluşturan birçok çubuğa sahiptir. Bunun distal ve proksimal ucu arasında stent uzunluğu ve geçit olarak stent lümeni 5 uzanır. Stent, dilate edilmiş yani serbest bırakılmış durumda uygun bir çapa ulaşır. Hemokompatibilitenin kolaylaştırılması için stent yüzeyi hidrofil yapıdadır.
