Haiyan Kangyuan Medical Instrument Co., Ltd. yakabudirira kuwana European Union Medical Device Regulation 2017/745 (inonzi "MDR") CE certification musi waChikunguru 19, 2023, chitupa nhamba 6122159CE01, iyo certification scope ndeye Urinary Catheters yeKushandisa Kamwechete. Foley), Kunyanya inosanganisira 2 nzira silicone foley catheter, 3 nzira silicone foley catheter, 2 nzira silicone foley catheter ine tiemann tip uye 3 nzira silicone foley catheter ine coude tip.Parizvino, Kangyuan Medical yakapfuura MDR zvigadzirwa:

Endotracheal Tubes for single Use;

Sterile Suction Catheters Yekushandisa Kamwechete;

Oxygen Masks for single Use;

Nasal Oxygen Cannulas for Single Use;

Guedel Airways nokuda Single Use;

Laryngeal Mask Airways;

Anesthesia Masks eKushandisa Kamwechete;

Mafirita ekufema eKushandisa Imwe;

Kufema Circuits nokuda Single Use;

Urinary Catheters Yekushandisa Kamwechete (Foley).

Chitupa cheEU MDR chinoratidza kuti Kangyuan Medical zvigadzirwa zvinosangana nezvinodiwa zvezvino zvino EU zvekurapa mudziyo mutemo 2017/745, zvine mamiriro ekupedzisira emusika weEU, uye zvinogona kuramba zvichitengeswa zviri pamutemo mumisika yemhiri kwemakungwa, zvichiisa hwaro hwakasimba hwe. kuwedzera kupinda mumusika weEurope uye nekusimudzira maitiro ekudyidzana nedzimwe nyika.