803 医疗器械报告 MEDICAL DEVICE REPORTING 806 医疗器械;改正与移动的报告 MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS 807 对器械的制造者与首次进口者的机构登记与器械列表 ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES 808 对州和地方医疗器械要求的...
食品和药物. 第803部分:医疗器械报告. 第803.13节:我需要提交英文报告吗? Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.13:Do I need to submit reports in English? CFR 21-803.13-2014 发布历史 CFR 21-803.13-2014由US-CFR-file 发布于 2014-02-14,并于 2014-02-...
第803部分:医疗器械报告. 第803.52节:如果我是一个进口商,我必须在我个人的不良事件报告提交哪些资料? Food and Drugs. Part803:Medical device reporting; (Eff. Until 8-14-15). Section803.52:If I am a manufacturer, what information must I submit in my individual adverse event reports? 被代替 2014...
中文标准名称:CFR 21-803.53-2014 食品和药物. 第803部分:医疗器械报告. 第803.53节:如果我是一个制造商,在何种情况下,我必须提交一份为期5天的报告? 英文标准名称:Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.53:If I am a manufacturer, in which circumstances must I...
803 医疗器械报告 MEDICAL DEVICE REPORTING 806 医疗器械;改正与移动的报告 MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS 807 对器械的制造者与首次进口者的机构登记与器械列表 ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES 808 对州和地方医疗器械要求的...
(a),(c),and(f)).NOTETO§801.437:Paragraphs(f)and(g)arestayeduntilJune27,1999,asthoseregula-tionsrelatetodevicepackagingthatuses‘‘coldseal’’adhesives.[62FR51029,Sept.30,1997,asamendedat63FR46175,Aug.31,1998]PART803—MEDICALDEVICEREPORTINGSubpartA—GeneralProvisionsSec.803.1Whatdoesthispart...
(a),(c),and(f)).NOTETO§801.437:Paragraphs(f)and(g)arestayeduntilJune27,1999,asthoseregula-tionsrelatetodevicepackagingthatuses‘‘coldseal’’adhesives.[62FR51029,Sept.30,1997,asamendedat63FR46175,Aug.31,1998]PART803—MEDICALDEVICEREPORTINGSubpartA—GeneralProvisionsSec.803.1Whatdoesthispart...
第H分章―医疗器械(SUBCHAPTER H―MEDICAL DEVICES) 800 总则 GENERAL? ? 801 标识 LABELING? ? 803 医疗器械报告 MEDICAL DEVICE REPORTING? ? 806 医疗器械;改正与移动的报告 MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS? ? 807 对器械的制造者与首次进口者的机构登记与器械列表 ESTABLISHMENT ...
803 医疗器械报告 MEDICAL DEVICE REPORTING 806 医疗器械;改正与移动的报告 MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS 807 对器械的制造者与首次进口者的机构登记与器械列表 ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES ...