Purchaser’s right to repair medical equipment under COVID-19 pandemic

P. Likhter
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Abstract

The article discusses certain aspects of the buyers rights to repair medical equipment during and after the expiration of the warranty period. Today, increasingly, some manufacturers limit the possibility of independent repairs by unreasonably highly integrating parts, technically unjustified complication of components, creating an artificial scarcity of spare parts in the market, preventing the work of independent service organizations and other controversial marketing strategies. The objectives of the study is to assess the limitations of the buyers rights to repair for the proposal of law enforcement proposals for respecting the balance of interests of the Parties under the Agreement; the elimination of the possibility of distorting civil law principles of conscientiousness and transparency. The tasks are permitted through the formal legal, regulatory, systemic, logical, comparative and theoretical and prognostic methods. According to the results of the work, the conclusions are formulated about the need to adjust the current legislation, including in the scope of manufacturers for the use of software that limits the repair of goods; unreasonably high degree of integration of blocks; failure to submit service documentation, as well as for electronic blocking of diagnostics, maintenance and repair of goods.
买方在COVID-19大流行期间维修医疗设备的权利
本文论述了医疗器械保修期内及保修期后买方维修权的若干问题。今天,越来越多的制造商限制了独立维修的可能性,通过不合理的高度集成部件,技术上不合理的组件复杂性,在市场上人为地造成备件稀缺,阻止独立服务组织的工作和其他有争议的营销策略。这项研究的目的是评估买方修葺权的限制,以便为尊重《协定》下各方的利益平衡而提出执法建议;消除了歪曲民事法律的尽责性和透明性原则的可能性。这些任务是通过正式的法律、监管、系统、逻辑、比较、理论和预测方法来允许的。根据工作结果,制定了关于需要调整现行立法的结论,包括在制造商使用软件的范围内限制修理商品;块的集成度不合理;未能提交服务文件,以及电子阻塞诊断,维护和修理货物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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