Akuti Haiyan Kangyuan Medical Instrument Co., Ltd. adapeza bwino satifiketi ya CE ya EU Medical Device Regulation 2017/745 (yotchedwa "MDR") pazinthu ziwiri mwezi watha. Zogulitsazo ndi PVC Laryngeal Mask Airways ndi Latex Foley Catheters Zogwiritsa Ntchito Pamodzi. Pakali pano, mankhwala 12 a Kangyuan Medical adutsa satifiketi ya MDR, yomwe ili motere:

[Endotracheal Tubes for single];

[Ma Catheters Osabala Ogwiritsidwa 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]

 

Satifiketi ya EU MDR ikuwonetsa kuti mankhwala a Kangyuan Medical amakwaniritsa zofunikira za malamulo aposachedwa a zida zamankhwala ku EU 2017/745 ndipo ali ndi njira zaposachedwa zopezera msika wa EU. Izi si kuzindikira mkulu wa khalidwe, chitetezo ndi mphamvu ya mankhwala Kangyuan mankhwala, komanso chithunzi chofunika kwambiri cha mphamvu luso kampani ndi mpikisano msika. Kangyuan Medical atenga mwayi uwu kukulitsa msika ku Europe ndikupereka chithandizo chamankhwala apamwamba kwa odwala ambiri padziko lonse lapansi.