CE/MDR ISO 13485 certificate

29-03-2022

CE/MDR, Pursuant to Regulation (EU) 2017/745 on Medical Devices, Annex XI Part A.


EN 1SO 13485:2016 is medical devices-Quality management systems-Requirements for regulatory purposes DIN EN ISO 13485:2016.


Hubei YI-YA got the updated CE/MDR and ISO 13485 cert on March, 22nd, 2022. 

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