MEDICAL DEVICE REPORTING的意思|示意

美 / / 英 / /

医疗器械报告

MEDICAL DEVICE REPORTING的网络常见释义

医疗器械报告 标识 LABELING 医疗器械报告 MEDICAL DEVICE REPORTING 医疗器械；改正与移动的报告 MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS ..

MEDICAL DEVICE REPORTING相关短语

1、 medical device reporting system 医疗器械报告系统

2、 mdr medical device reporting system 医疗器械报告系统

MEDICAL DEVICE REPORTING相关例句

These complaints shall be evaluated to determine whether or not they require reporting to FDA under 21 CFR part 804 or 803, Medical Device reporting.

应对这些投诉进行评估，并根据医疗器械报告制度(联邦法规21篇804或803部)要求决定它们是否需要向FDA报告。

These requirements include establishment registration, medical device listing, quality system, medical device reporting, premarket approval or clearance, labeling and U. s. agent requirements.

这些规定包括工厂的注册，医疗设备清单，质量系统，医疗设备报告，售前批准或者认可，商标及美国代理的要求。