DIN 96073:2009 医疗器械.双面压舌钳
Medical instruments - Tongue depressor, double-ended
DIN 96073:2021 医疗器械. 双面压舌钳
The project defines dimensions and marking of double-ended tongue depressors, as used in surgery and public health service
Medical instruments - Tongue depressor, double-ended
ASTM F813-01 医疗器械材料直接接触细胞培养评估标准实践
1.1 This practice describes a reference method of direct contact cell culture testing which may be used in evaluating the cytotoxic potential
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
ASTM F813-83(1996)e1 医疗器械材料直接接触细胞培养评估标准实践
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
ASTM F813-20 医疗器械材料直接接触细胞培养评估标准实践
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
DIN 96115:2010 医疗器械.计量表型分析器
Medical instruments - Gauges type Lexer
DIN 58861:1976 医疗器械.Lambotte式平面凿子
Medical instruments; osteotomes type Lambotte Instruments médicaux; ciseaux de Lambotte
Medical instruments; osteotomes type Lambotte
YY/T 91051-1999 医疗器械行业标准体系表
System table for standard of medical devices
GOST ISO 14971-2011 医疗器械.医疗器械风险管理应用
Medical devices. Application of risk management to medical devices
DIN 13115:2006 医疗器械.平面弯曲指甲剪
The project defines dimensions and marking of nail scissors, curved on flat, as used in surgery, public health service or armed forces
Medical instruments - Nail scissors, curved on flat
YY/T 0316-2016 医疗器械 风险管理对医疗器械的应用
本标准为制造商规定了一个过程，以识别与医疗器械[包括体外诊断(IVD)医疗器械]有关的危险(源)，估计和评价相关的风险，控制这些风险，并监视控制的有效性。本标准的要求适用于医疗器械生命周期的所有阶段。本标准不用于临床决策。本标准不规定可接受的风险水平。本标准不要求制造商有一个适当的质量体系。然而
Medical devices.Application of risk management to medical devices
GB/T 42062-2022 医疗器械 风险管理对医疗器械的应用
Medical devices—Application of risk management to medical devices
YY/T 0316-2008 医疗器械.风险管理对医疗器械的应用
本标准为制造商规定了一个过程，以判定与医疗器械，包括体外诊断（IVD）医疗器械有关的危害，估计和评价相关的风险，控制这些风险，并监视控制的有效性。 本标准的要求适用于医疗器械生命周期的所有阶段。 本标准不用于临床决策。 本标准不规定可接受的风险水平。 本标准不要求制造商有一个适当的质量体系
Medical devices.Application of risk management to medical devices
BS EN 62366-1:2015 医疗器械. 医疗器械可用性工程应用
Medical devices. Application of usability engineering to medical devices
BS EN 62366-1:2015+A1:2020 医疗器械. 医疗器械可用性工程应用
Medical devices. Application of usability engineering to medical devices
DIN 96073:2009 医疗器械.双面压舌钳
Medical instruments - Tongue depressor, double-ended
DIN 96073:2021 医疗器械. 双面压舌钳
The project defines dimensions and marking of double-ended tongue depressors, as used in surgery and public health service
Medical instruments - Tongue depressor, double-ended
ASTM F813-01 医疗器械材料直接接触细胞培养评估标准实践
1.1 This practice describes a reference method of direct contact cell culture testing which may be used in evaluating the cytotoxic potential
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
ASTM F813-83(1996)e1 医疗器械材料直接接触细胞培养评估标准实践
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
ASTM F813-20 医疗器械材料直接接触细胞培养评估标准实践
Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
DIN 96115:2010 医疗器械.计量表型分析器
Medical instruments - Gauges type Lexer
DIN 58861:1976 医疗器械.Lambotte式平面凿子
Medical instruments; osteotomes type Lambotte Instruments médicaux; ciseaux de Lambotte
Medical instruments; osteotomes type Lambotte
YY/T 91051-1999 医疗器械行业标准体系表
System table for standard of medical devices
GOST ISO 14971-2011 医疗器械.医疗器械风险管理应用
Medical devices. Application of risk management to medical devices
DIN 13115:2006 医疗器械.平面弯曲指甲剪
The project defines dimensions and marking of nail scissors, curved on flat, as used in surgery, public health service or armed forces
Medical instruments - Nail scissors, curved on flat
YY/T 0316-2016 医疗器械 风险管理对医疗器械的应用
本标准为制造商规定了一个过程，以识别与医疗器械[包括体外诊断(IVD)医疗器械]有关的危险(源)，估计和评价相关的风险，控制这些风险，并监视控制的有效性。本标准的要求适用于医疗器械生命周期的所有阶段。本标准不用于临床决策。本标准不规定可接受的风险水平。本标准不要求制造商有一个适当的质量体系。然而
Medical devices.Application of risk management to medical devices
GB/T 42062-2022 医疗器械 风险管理对医疗器械的应用
Medical devices—Application of risk management to medical devices
YY/T 0316-2008 医疗器械.风险管理对医疗器械的应用
本标准为制造商规定了一个过程，以判定与医疗器械，包括体外诊断（IVD）医疗器械有关的危害，估计和评价相关的风险，控制这些风险，并监视控制的有效性。 本标准的要求适用于医疗器械生命周期的所有阶段。 本标准不用于临床决策。 本标准不规定可接受的风险水平。 本标准不要求制造商有一个适当的质量体系
Medical devices.Application of risk management to medical devices
BS EN 62366-1:2015 医疗器械. 医疗器械可用性工程应用
Medical devices. Application of usability engineering to medical devices
BS EN 62366-1:2015+A1:2020 医疗器械. 医疗器械可用性工程应用
Medical devices. Application of usability engineering to medical devices
编辑：北检院编辑部
