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医疗器械生物学评价 第11部分：全身毒性试验

Biological evaluation of medical devices Part 11 : Tests for systemic toxicity

医疗器械的生物评估.与血液相互作用的试验选择

Biological evaluation of medical devices. Selection of tests for interactions with blood

医疗应用冷大气压等离子体(CAP)产生用等离子体源的通用要求

General requirements for plasma sources for the generation of cold atmospheric pressure plasma (CAP) for medical applications

牙科 牙科器械材料 第2部分：聚合物

Dentistry - Materials for dental instruments - Part 2: Polymers

医疗器械生物学评价 第4部分：与血液相互作用医疗器械评价方法的选择（ISO 10993-4:2017）

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)

外科植入物 可吸收植入物 可吸收金属植入物评估的通用指南和要求

Implants for surgery — Absorbable implants — General guidelines and requirements for assessment of absorbable metallic implants

可吸收医疗器械的生物学评价 一般要求

Biological evaluation of absorbable medical devices. General requirements

医用美利体育官网首页网址的生物学评估 第16部分：降解产物和浸出物的毒性动力学研究设计（ISO 10993-16:2017）

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)

医疗保健应用中呼吸气体通路的生物相容性评估 第1部分：风险管理流程内的评估和测试 (ISO 18562-1:2017)

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1: Evaluation and testing within a risk management process (ISO 18562-1:2017)

医疗器械的生物学评估 第18部分：风险管理流程中医疗器械材料的化学特性

Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)