中文Posachedwapa, Haiyan Kangyuan MedicalChida Co., Ltd. yapeza bwino satifiketi ya CE ya EU Medical Device Regulation 2017/745 (yotchedwa "MDR") ya "open-t" ina.ip catheter yamkodzo (yomwe imadziwikanso kuti: nephrostomy chubu)" mankhwala. Pakalipano, Kangyuan Medical ali ndi zinthu 13 zomwe zadutsa chiphaso cha MDR,monga pansipa:
[Endotracheal Tubes for single];
[Ma Catheters Osabala Omwe Amagwiritsidwa Ntchito Pamodzi];
[Masks Oxygen Ogwiritsidwa Ntchito Pamodzi];
[Ma Cannula a Oxygen a M'mphuno Ogwiritsa Ntchito Kamodzi];
[Guedel Airways for Single Use];
[Laryngeal Mask Airways];
[Masks a Anesthesia Ogwiritsa Ntchito Pamodzi];
[Zosefera Zopumira Zogwiritsa Ntchito Pamodzi];
[Magawo Opumira Ogwiritsa Ntchito Pamodzi];
[Ma Catheter a Mkodzo Ogwiritsa Ntchito Pamodzi (Foley)];
[Latex Foley Catheters Ogwiritsa Ntchito Pamodzi];
[PVC Laryngeal Mask Airways];
[Ma Catheter a Suprapubic Ogwiritsidwa Ntchito Pamodzi]
Kupeza chiphaso cha EU MDR sikungotanthauza kuti Kangyuan Medical wapambana "chiphaso" ku msika wa EU ndi mfundo zokhwima, komanso zimasonyeza kuti Kangyuan wafika pamtunda wotsogola padziko lonse m'munda wa zipangizo zamankhwala. Chitsimikizo cha EU MDR chili ndi zofunika kwambiri pamtundu wazinthu, magwiridwe antchito achitetezo, zidziwitso zachipatala ndi zina. Kangyuan Medical luso pochitika certification limasonyeza amphamvu luso mphamvu ndi apamwamba mankhwala khalidwe. Chitsimikizo cha MDR chidzathandiza Kangyuan Medical kutsegula kwambiri msika wa EU ndikuwonjezera mbiri yapadziko lonse lapansi. Pa nthawi yomweyo, amalimbikitsanso Kangyuan Medical mosalekeza kuzamitsa luso kasamalidwe kutsatira, imathandizira luso lamakono, ndi kulimbikitsa masanjidwe ake mayiko njira ndi mfundo zapamwamba, motero kumanga olimba mzere chitetezo kwa thanzi ndi chitetezo cha ogula padziko lonse.
Nthawi yotumiza: May-14-2025