SS-EN ISO 10993-5:2009医疗器械生物学评价第5部分:体外细胞毒性试验(ISO10993-5:2009)UNE-EN ISO 10993-5:2009医疗器械的生物学评价第5部分:体外细胞毒性试验(ISO10993-5:2009)NS-EN ISO 10993-5:2009医疗器械的生物学评价第5部分:体外细胞毒性测试(ISO10993-5:2009)AENOR UNE-EN ISO 10993-5:2009医疗器...
BS EN ISO 10993-5:2009的仪器设备信息,ISO 10993 的这一部分描述了评估医疗器械体外细胞毒性的测试方法。 这些方法指定直接或通过扩散与装置和/或装置提取物接触的培养细胞的孵育。 这些方法旨在使用适当的生物参数确定哺乳动物细胞体外的生物反应。 This part of ISO 1099
BS EN ISO 10993-5:2009
BS EN ISO10993-15:2009ICS 11.100.20NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBRITISH STANDARDBiological evaluationof medical devicesPart 15: Identification andquantification of degradationproducts from metals and alloys (ISO10993-15:2000)...
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BSENISO10993-1:009ICS11.100.0NOCOPYINGWITHOUTBSIPERMISSIONEXCEPTASPERMITTEDBYCOPYRIGHTLAWBRITISHSTANDARDBiologicalevaluationofmedicaldevicesPart1:SamplepreparationandreferencematerialsISO10993-1:007
BS EN ISO10993-1:2009ICS 11.100.20NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBRITISH STANDARDBiological evaluationof medical devicesPart 1: Evaluation and testing (ISO10993-1:2003)Licensed copy: Vocational Trading Council, Vocational Training Council, Version correct as of ...
BS EN ISO 10993-1-2009 (2010) British Standard European Standard英国标准欧盟标准国际标准英文版电子版Part 2 下载积分: 1800 内容提示: ISO 10993-1:2009(E) 7 c) Breached or compromised surfaces ⎯ devices that contact breached or otherwise compromised body surfaces. EXAMPLES Dressings or healing ...
BS EN ISO 10993-17:2023 购买 正式版 本文件规定了医疗器械成分毒理学风险评估的流程和要求。还规定了用于评估接触某种成分是否不会造成明显危害的方法和标准。毒理学风险评估可以作为最终产品生物学评估的一部分,如 ISO 10993-1 所述。本文件中描述的过程适用于根据 ISO 10993-18 获得的化学特性信息。当需要对...
To reduce the likelihood of adverse reactions and ultimately to make medical devices safer, BS EN ISO 10993-10:2023 Biological evaluation of medical devices — Part 10: Tests for skin sensitization specifies procedures for assessing devices and their constituent materials for their potential to induce...