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This part of ISO 10993 provides general requirements for the design of tests in a simulated environment for identifying and quantifying degradation
Biological evaluation of medical devices. Part 13: Identification and quantification of degradation products from polymeric medical devices
GB/T16886的本部分为准备用于临床的成品聚合物医疗器械的降解产物的定性与定量试验设计提供了指南。 GB/T16886的本部分描述了两种生成降解产物的试验方法，一是作为筛选方法的加速降解试验，另一是实际时间降解试验。对在使用时方进行聚合的材料，试验时使用固化的聚合物。试验所得数
Biological evaluation of medical devices--Part 13:Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices—Part 13: Identification and quantification of degradation products from polymeric medical devices
Évaluation biologique des dispositifs médicaux - Partie 13 : identification et quantification de produits de dégradation de dispositifs médicaux à base de polymères
This part of ISO 10993 provides general requirements for the design of tests in a simulated environment for identifying and quantifying degradation
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
This part of ISO 10993 provides guidance on general requirements for the design of tests for identifying and quantifying degradation products from
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
이 규격은 임상용으로 준비된 고분자성 의료기기에서 나온 분해 산물의 확인 및 정량을 위한
Biological evaluation of medical devices－Part 13：Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices - Part 13 : identification and quantification of degradation products from polymeric medical devices
Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010); German version EN ISO 10993-13:2010
Biological Evaluation of Medical Devices - Part 13: Identification and Quantification of Degradation Products from Polymeric Medical Devices First Edition; ISO 10993-13: 1998
Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices / Note: To be replaced by GOST R ISO 10993-13 (2009).
This part of ISO 10993 provides general requirements for the design of tests in a simulated environment for identifying and quantifying degradation
Biological evaluation of medical devices. Part 13: Identification and quantification of degradation products from polymeric medical devices
GB/T16886的本部分为准备用于临床的成品聚合物医疗器械的降解产物的定性与定量试验设计提供了指南。 GB/T16886的本部分描述了两种生成降解产物的试验方法，一是作为筛选方法的加速降解试验，另一是实际时间降解试验。对在使用时方进行聚合的材料，试验时使用固化的聚合物。试验所得数
Biological evaluation of medical devices--Part 13:Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices—Part 13: Identification and quantification of degradation products from polymeric medical devices
Évaluation biologique des dispositifs médicaux - Partie 13 : identification et quantification de produits de dégradation de dispositifs médicaux à base de polymères
This part of ISO 10993 provides general requirements for the design of tests in a simulated environment for identifying and quantifying degradation
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
This part of ISO 10993 provides guidance on general requirements for the design of tests for identifying and quantifying degradation products from
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices
이 규격은 임상용으로 준비된 고분자성 의료기기에서 나온 분해 산물의 확인 및 정량을 위한
Biological evaluation of medical devices－Part 13：Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices - Part 13 : identification and quantification of degradation products from polymeric medical devices
Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010); German version EN ISO 10993-13:2010
Biological Evaluation of Medical Devices - Part 13: Identification and Quantification of Degradation Products from Polymeric Medical Devices First Edition; ISO 10993-13: 1998
Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices / Note: To be replaced by GOST R ISO 10993-13 (2009).
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