发布时间：2024-05-27 17:49:26 - 更新时间：2024年06月29日 15:22
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This part 2-1 of EN 45502 specifies requirements that are applicable to those active implantable medical devices intended to treat bradyarrhytmias
Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (Cardiac pacemakers)
Active implantable medical devices -- Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
Active implantable medical devices -- Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
Implants for surgery—Active implantable medical devices—Part 2: Cardiac pacemakers
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
Implants for surgery－Active implantable medical devices－Part 4：Implantable infusion pumps
本文件规定了有源植入式循环支持器械的型式试验、动物实验研究及临床评价的基本要求。本文件适用于心室辅助装置包括左心辅助、右心辅助，全人工心脏，双心室辅助装置，经皮辅助装置，儿科辅助装置等有源植入式循环支持器械。本文件同样适用于有源植入式循环支持器械的部分非植入部件和附件。本文件不适用于生产过程中的常规
Active implantable medical devices -- Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
Implants for surgery－Active implantable medical devices－Part 5：Circulatory support devices
Implants for surgery－Active implantable medical devices－Part 3：Implantable neurostimulators
Implants for surgery — Active implantable medical devices —Part 3: Implantable neurostimulators
This Technical Specification contains test methods that are applicable to a broad class of active implantable medical devices (AIMDs) for the purpose
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
This part 2-1 of EN 45502 specifies requirements that are applicable to those active implantable medical devices intended to treat bradyarrhytmias
Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (Cardiac pacemakers)
Active implantable medical devices -- Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
Active implantable medical devices -- Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
Implants for surgery—Active implantable medical devices—Part 2: Cardiac pacemakers
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
Implants for surgery — Active implantable medical devices — Part 2: Cardiac pacemakers
Implants for surgery－Active implantable medical devices－Part 4：Implantable infusion pumps
本文件规定了有源植入式循环支持器械的型式试验、动物实验研究及临床评价的基本要求。本文件适用于心室辅助装置包括左心辅助、右心辅助，全人工心脏，双心室辅助装置，经皮辅助装置，儿科辅助装置等有源植入式循环支持器械。本文件同样适用于有源植入式循环支持器械的部分非植入部件和附件。本文件不适用于生产过程中的常规
Active implantable medical devices -- Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
Implants for surgery－Active implantable medical devices－Part 5：Circulatory support devices
Implants for surgery－Active implantable medical devices－Part 3：Implantable neurostimulators
Implants for surgery — Active implantable medical devices —Part 3: Implantable neurostimulators
This Technical Specification contains test methods that are applicable to a broad class of active implantable medical devices (AIMDs) for the purpose
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
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