MDD Thiab MDR Dab Tsi?

Jul 02, 2021 Tso lus

European Union Medical Device Directive (MDD) tau nyob hauv yuav luag 25 xyoo ua ntej nws tau hloov los ntawm European Union Medical Device Regulation (MDR) tshiab, tau tshaj tawm xyoo 2017. Cov lus qhia yav dhau los no tau tsim los rau EU lub hauv paus rau cov cuab yeej siv kho mob, tab sis nws tsis suav nrog hauv vitro cov cuab yeej siv tshuaj kho mob.

Txawm li cas los xij, nws tau txiav txim siab tias yuav tsum tau kho dua tshiab ntawm cov lus qhia no yog tsim nyog los tsim kom muaj kev ruaj khov dua, pob tshab, ruaj khov, thiab muaj peev xwm kwv yees tau. Lub hom phiaj yog txhawm rau txhim kho qib kev noj qab haus huv thiab kev nyab xeeb ntawm cov cuab yeej siv kho mob, thaum tseem txhawb nqa kev hloov pauv tshiab hauv kev lag luam.


Jinhua Huacheng Medical Appliance Co., Ltd.

Kev tsim cov khoom siv kho mob pov tseg:Electrosurgical mem hluav, phaj hauv av, tawv tawv thiab ECG electrode

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