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医用级超高分子量聚乙烯纱标准规范

Standard Specification for Medical-Grade Ultra-High-Molecular-Weight Polyethylene Yarns

医用超高分子量聚乙烯纱线标准规范

Standard Specification for Medical-Grade Ultra-High-Molecular-Weight Polyethylene Yarns

用全身注射法评估材料提取物的急性全身毒性的标准实施规程 在老鼠身上

Standard Practice for Evaluating Acute Systemic Toxicity of Material Extracts by Systemic Injection in the Mouse

医疗器械用长期植入材料对肌肉和骨组织反应评估的标准实施规程

Standard Practice for Assessment of Muscle and Bone Tissue Responses to Long-Term Implantable Materials Used in Medical Devices

细胞培养测试方法

Cell culture test methods

医疗保健应用中呼吸气体通路的生物相容性评估 第4部分：冷凝水中可浸出物的测试

Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 4: Tests for leachables in condensate

医疗保健应用中呼吸气体通道的生物相容性评估 在风险管理流程中进行评估和测试

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Evaluation and testing within a risk management process

医疗器械的生物学评价 第2部分：动物福利要求（ISO 10993-2:2022）

Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)

医疗保健应用中呼吸气体通路的生物相容性评估 第3部分：挥发性有机化合物（VOC）排放测试（ISO 18562-3:2017）

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 3: Tests for emissions of volatile organic compounds (VOCs) (ISO 18562-3:2017)

医疗保健应用中呼吸气体路径的生物相容性评估 第4部分：冷凝水中可浸出物的测试

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 4: Tests for leachables in condensate (ISO/DIS 18562-4:2022); German and English version prEN ISO 18562-4:2022 / Note: Date of issue 2022-11-18*Intended as replacem...

牙科学.牙科用医疗器械生物相容性评价(ISO 7405-2008+Amd. 1-2013).德文版本DIN EN ISO 7405-2008+A1-2013

Dentistry - Evaluation of biocompatibility of medical devices used in dentistry (ISO 7405:2008 + Amd. 1:2013); German version EN ISO 7405:2008 + A1:2013

医疗器械生物学评价 第10部分：刺激与皮肤致敏试验

Biological evaluation of medical devices—Part 10: Tests for irritation and skin sensitization

医疗器械的生物学评价.第2部分:动物福利要求

Biological evaluation of medical devices — Part 2: Animal welfare requirements

医疗器械的生物学评价. 第6部分: 植入后的局部效果试验

Biological evaluation of medical devices - Part 6: Tests for local effects after implantation

医疗器械的生物学评价.第7部分:环氧乙烷灭菌残留物.勘误表1

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals; Technical Corrigendum 1

医疗保健应用中呼吸气体通路的生物相容性评估

Biocompatibility evaluation of breathing gas pathways in healthcare applications

医疗保健应用中呼吸气体通道的生物相容性评估. 第3部分: 挥发性有机化合物(VOC)排放试验

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 3: Tests for emissions of volatile organic compounds (VOCs)

医疗保健应用中呼吸气体通道的生物相容性评估. 第4部分: 冷凝物中的析出物试验

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 4: Tests for leachables in condensate

用于神经轴应用的导管系统 - 无菌和一次性导管及附件

Catheter systems for neuraxial application — Sterile and single-use catheters and accessories

麻醉和呼吸美利体育官网首页网址 麻醉储液袋

Anaesthetic and respiratory equipment – Anaesthetic reservoir bags

外科植入物.陶瓷材料.第2部分:含氧化锆增强的高纯氧化铝基复合材料

Implants for surgery — Ceramic materials — Part 2: Composite materials based on a high-purity alumina matrix with zirconia reinforcement

生物医学器械生物学评价 第2部分：动物福利要求（ISO 10993-2:2022）

Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)

牙科学 多功能手柄（ISO 22569:2020）

Dentistry - Multifunction handpieces (ISO 22569:2020)

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：风险管理过程中的评估和测试

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1 : evaluation and testing within a risk management process

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：风险管理过程中的评估和测试

Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1 : evaluation and testing within a risk management process

医疗器械生物学评价 - 第 2 部分：动物福利要求 (ISO 10993-2:2022)

Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)

医疗器械生物学评价 第2部分：动物福利要求

Biological evaluation of medical devices - Part 2: Animal welfare requirements