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表面接触医疗器械检测

发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22

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军工检测 其他检测

DIN 96073:2009 .双压舌钳

Medical instruments - Tongue depressor, double-ended

DIN 96073:2021 . 双压舌钳

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 材料直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 材料直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 材料直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 .计量型分析

Medical instruments - Gauges type Lexer

DIN 58861:1976 .Lambotte式平凿子

Medical instruments; osteotomes type Lambotte Instruments médicaux; ciseaux de Lambotte

Medical instruments; osteotomes type Lambotte

YY/T 91051-1999 行业标准体系

System table for standard of medical devices

GOST ISO 14971-2011 .风险管理应用

Medical devices. Application of risk management to medical devices

DIN 13115:2006 .平弯曲指甲剪

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 风险管理对的应用

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 风险管理对的应用

Medical devices—Application of risk management to medical devices

YY/T 0316-2008 .风险管理对的应用

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 . 可用性工程应用

Medical devices. Application of usability engineering to medical devices

BS EN 62366-1:2015+A1:2020 . 可用性工程应用

Medical devices. Application of usability engineering to medical devices

DIN 96073:2009 .双压舌钳

Medical instruments - Tongue depressor, double-ended

DIN 96073:2021 . 双压舌钳

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 材料直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 材料直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 材料直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 .计量型分析

Medical instruments - Gauges type Lexer

DIN 58861:1976 .Lambotte式平凿子

Medical instruments; osteotomes type Lambotte Instruments médicaux; ciseaux de Lambotte

Medical instruments; osteotomes type Lambotte

YY/T 91051-1999 行业标准体系

System table for standard of medical devices

GOST ISO 14971-2011 .风险管理应用

Medical devices. Application of risk management to medical devices

DIN 13115:2006 .平弯曲指甲剪

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 风险管理对的应用

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 风险管理对的应用

Medical devices—Application of risk management to medical devices

YY/T 0316-2008 .风险管理对的应用

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 . 可用性工程应用

Medical devices. Application of usability engineering to medical devices

BS EN 62366-1:2015+A1:2020 . 可用性工程应用

Medical devices. Application of usability engineering to medical devices

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