Haiyan Kangyuan Medical Instrument Co., Ltd. adalandira bwino chiphaso cha European Union Medical Device Regulation 2017/745 (chotchedwa "MDR") CE certification pa Julayi 19, 2023, nambala ya satifiketi 6122159CE01, kuchuluka kwa certification ndi Urinary Catheters for Single Use Foley), Makamaka 2 njira silikoni foley catheter, 3 njira silikoni foley catheter, 2 njira silikoni foley catheter ndi tiemann nsonga ndi 3 njira silikoni foley catheter ndi coude nsonga.Pakali pano, Kangyuan Medical wadutsa mankhwala MDR:

Machubu a Endotracheal Ogwiritsidwa Ntchito Pamodzi;

Ma Catheters Osabala Omwe Amagwiritsidwa Ntchito Pamodzi;

Masks Oxygen Ogwiritsidwa Ntchito Pamodzi;

Ma Cannula Oxygen A M'mphuno Yogwiritsidwa Ntchito Pamodzi;

Guedel Airways kwa Single Ntchito;

Laryngeal Mask Airways;

Masks a Anesthesia Ogwiritsa Ntchito Pamodzi;

Zosefera Zopumira Zogwiritsa Ntchito Limodzi;

Madera Opumira Ogwiritsa Ntchito Limodzi;

Ma Catheters Ogwiritsa Ntchito Pamodzi (Foley).

Chitsimikizo cha EU MDR chikuwonetsa kuti mankhwala a Kangyuan Medical akukwaniritsa zofunikira za malamulo aposachedwa a EU 2017/745, ali ndi njira zamakono zopezera msika wa EU, ndipo akhoza kupitiliza kugulitsidwa mwalamulo m'misika yakunja yakunja, ndikuyika maziko olimba kulowanso msika waku Europe ndikulimbikitsa njira yolumikizirana mayiko.