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Oferowany aparat USG musi:\na. stanowi\u0107 wyr\u00f3b medyczny w rozumieniu rozporz\u0105dzenia Parlamentu Europejskiego i Rady UE 2017/745 z dnia 5 kwietnia 2017 r. w sprawie wyrob\u00f3w medycznych oraz musi by\u0107 dopuszczony do obrotu i u\u017cywania zgodnie z obowi\u0105zuj\u0105cymi przepisami prawa,\nb. by\u0107 sprz\u0119tem fabrycznie nowym, kompletnym, nieu\u017cywanym, nierekondycjonowanym, niepowystawowym, w pe\u0142ni sprawnym oraz wyprodukowanym nie wcze\u015bniej ni\u017c w 2025 r.,\nc. spe\u0142nia\u0107 wymagania okre\u015blone przez Zamawiaj\u0105cego w Zapytaniu ofertowym, w szczeg\u00f3lno\u015bci warunki graniczne okre\u015blone w Opisie przedmiotu zam\u00f3wienia stanowi\u0105cym za\u0142\u0105cznik nr 1 do ZO;\nd. odpowiada\u0107 standardom jako\u015bciowym i technicznym wynikaj\u0105cym z jego funkcji i przeznaczenia;\ne. by\u0107 wolny od wad materia\u0142owych, konstrukcyjnych, fizycznych i prawnych;\nf. nie by\u0107 obci\u0105\u017cony prawami os\u00f3b trzecich;\ng. nie wymaga\u0107 do uruchomienia i prawid\u0142owego dzia\u0142ania zakupu dodatkowych element\u00f3w, akcesori\u00f3w ani licencji, poza standardowym osprz\u0119tem jednorazowym, je\u017celi taki osprz\u0119t jest typowo wymagany do eksploatacji;\nh. posiada\u0107 oznakowanie CE oraz aktualn\u0105 dokumentacj\u0119 zgodno\u015bci w\u0142a\u015bciw\u0105 dla statusu regulacyjnego oferowanego wyrobu;\n\n3. 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