Active implantable medical devices - Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators) Ingestion-build-115288 BS IEC 62243 defines formal

BS IEC 62243 defines formal specifications for supporting system diagnosis

The wedge tensile test and hardness test have been improved

BS EN 16571 has been prepared as part of the EU RFID Mandate M/436

The primary audience for this Guide is laboratory staff who are required to prepare and use materials for specific in-house quality control applications

is used to prevent the entry of dust which might otherwise lead to the formation of a combustible mixture within enclosures that do not contain a source of combustible dust

Active implantable medical devices - Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators) Ingestion-build-115288 BS IEC 62243 defines formal1 Scope This Part 2 2 of EN 45502 specifies requirements that are applicable to implantable cardioverter defibrillators and the functions of active implantable medical devices intended to treat tachyarrhythmia. The tests that are specified in EN 45502 are type tests and are to be carried out on samples of a device to show compliance. This part of EN 45502 is also applicable to some non implantable parts and accessories of the devices (see Note 1). The