Talu ai nei, Haiyan Kangyuan MedicalMeafaigaluega Co., Ltd. ua manuia le mauaina o le tusi faamaonia o le CE o le EU Medical Device Regulation 2017/745 (faʻaigoaina o le "MDR") mo se isi "tatala-tip urinary catheter (lea e lauiloa foi: nephrostomy tube) "oloa. I le taimi nei, ua maua e Kangyuan Medical 13 oloa ua pasia le tusi faamaonia MDR,pei o lalo:
[Endotracheal Tubes mo le Fa'aoga Tasi];
[Sterile Suction Catheters mo le Fa'aoga Tasi];
[Masinisi Okesene mo le Fa'aoga Ta'atasi];
[Nasal Oxygen Cannulas mo le Fa'aoga Tasi];
[Guedel Airways mo le Fa'aoga Ta'atasi];
[Laryngeal Mask Airways];
[Mafu fa'ama'i mo le Fa'aaogā Ta'atasi];
[Fili Manava mo Fa'aoga Ta'itasi];
[Li'o Manava mo le Fa'aaogā Ta'atasi];
[Urinary Catheters mo le Fa'aoga Tasi (Foley)];
[Latex Foley Catheters mo le Fa'aoga Tasi];
[PVC Laryngeal Mask Airways];
[Suprapubic Catheters mo le Fa'aoga Tasi]
O le mauaina o le EU MDR certification e le gata o lona uiga o le Kangyuan Medical ua manumalo i le "pasese" i le maketi a le EU ma tulaga saʻo, ae o loʻo faʻaalia ai foi ua ausia e Kangyuan le tulaga taʻutaʻua faavaomalo i le tulaga o masini faafomaʻi. O le EU MDR certification o loʻo i ai ni manaʻoga faʻapitoa mo le lelei o oloa, faʻatinoga saogalemu, faʻamatalaga falemaʻi ma isi vaega. O le mafaia e le Kangyuan Medical e pasia le tusipasi e faʻaalia ai lona malosi faʻapitoa faʻapitoa ma tulaga lelei o oloa. O le MDR certification o le a fesoasoani ia Kangyuan Medical e matua tatalaina le maketi a le EU ma faʻaleleia le igoa faʻavaomalo faavaomalo. I le taimi lava e tasi, e faʻamalosia ai foʻi le Kangyuan Medical e faʻaauau pea ona faʻalauteleina lona faʻatautaia o le tausisia o tomai faʻapitoa, faʻavavevave le faʻafouina o tekonolosi, ma faʻalauiloa lona faʻatulagaina faʻavaomalo faʻatasi ma tulaga maualuga, ma fausia ai se laina puipuiga sili atu mo le soifua maloloina ma le saogalemu o tagata faʻatau lalolagi.
Taimi meli: Me-14-2025
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