中文Munguva pfupi yapfuura, Haiyan Kangyuan MedicalChimbo Co., Ltd. yakabudirira kuwana CE certification chitupa cheEU Medical Device Regulation 2017/745 (inonzi "MDR") yeimwe "open-t".ip weti catheter (inozivikanwawo se: nephrostomy chubhu)" chigadzirwa. Parizvino, Kangyuan Medical ine zvigadzirwa gumi nezvitatu zvakapasa MDR certification,sepazasi:
[Endotracheal Tubes for single Use];
[Sterle Suction Catheters for single Use];
[Masiki Okisijeni Ekushandisa Kamwechete];
[Nasal Oxygen Cannulas for single Use];
[Guedel Airways yeKushandisa Kamwechete];
[Laryngeal Mask Airways];
[Masiki eAnesthesia Ekushandisa Kamwechete];
[Masefa Ekufema Ekushandisa Kamwechete];
[Kufema Denderedzwa Kwekushandisa Kamwechete];
[Urinary Catheters Yekushandisa Kamwechete (Foley)];
[Latex Foley Catheters Yekushandisa Kamwechete];
[PVC Laryngeal Mask Airways];
[Suprapubic Catheters yeKushandisa Kamwechete]
Kuwana certification yeEU MDR hakungorevi kuti Kangyuan Medical yakunda "kupasa" kumusika weEU zvine mwero wakasimba, asi zvakare zvinoratidza kuti Kangyuan yasvika padanho repamusoro repasi rose mumunda wezvigadzirwa zvekurapa. Iyo EU MDR certification ine zvakanyanya kuomarara zvinodiwa zvemhando yechigadzirwa, kuchengetedza kuita, data rekiriniki uye zvimwe zvinhu. Kangyuan Medical kugona kupasa certification inoratidza simba rayo rehunyanzvi uye rakatanhamara chigadzirwa chemhando. Iyo MDR certification ichabatsira Kangyuan Medical kuvhura zvakanyanya musika weEU uye kuwedzera mukurumbira wepasi rose. Panguva imwecheteyo, inokurudzirawo Kangyuan Medical kuti irambe ichidzamisa manejimendi ekutevedza kwehunyanzvi, kukurumidza kuvandudza tekinoroji, uye kusimudzira marongero ayo epasi rose ane mwero wepamusoro, nokudaro kuvaka tambo yakasimba yekudzivirira yehutano nekuchengetedzeka kwevatengi vepasirese.
Nguva yekutumira: May-14-2025