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- 欧洲议会和欧洲委员会体外诊断医疗器械指令Directive of the European Parliament and of the Council on in Vitro Diagnostic Medical Devices
- 实验室试验和体外诊断试验系统专业人员用体外诊断试验医疗器械厂商提供信息调整要求概要Clinical laboratory testing and in vitro diagnostic test systems - In vitro diagnostic medical devices for professional use - Summary of regulatory requirements for information supplied by the manufacturer
- 离体诊断医疗器械指令in vitro diagnostic medical device directive
- 体外诊断试剂in vitro diagnostic reagent
- 体外诊断用血库离心机Blood bank centrifuge for in vitro diagnostic use
- 基于核酸的体外诊断Nueleie acid-based IVDs
- 体外诊断用的强化培养基Potentiating media for in vitro diagnostic use
- 体外诊断试剂管理亟待加强Management of Diagnosis Regents should Strengthened
- 体外受孕vitro fertilization
- 体外诊断in vitro diagnosis(IVD)
- 体外标记in vitro labelling; labelled in vitro
- 体外测定in vitro assay
- 体外超滤extra-corporeal ultrafiltration
- 体外除颤external defibrillation
- 体外磁铁external magnet
- 体外复温external rewarming
- 体外灌注ECP; extracorporeal perfusion
- 体外活体supravital
- 体外计数in vitro counting; surface counting
- 体外接管extracorporeal tubing
