求 CEN/TR 17223:2018 EN ISO 13485: 2016(用於法規目的之醫療器材品
求 CEN/TR 17223:2018 Guidance on the relationship between EN ISO 13485: 2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation求 CEN/TR 17223:2018 EN ISO 13485: 2016(用於法規目的之醫療器材品質系統要求)與歐盟醫療器材法規及體外診斷醫療器材法規之關聯性指引
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