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Active implantable medical devices - Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers) Ingestion-build-258901 BS EN 12522-2

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BS EN 12522-2

and an introduction to the ISMS family of standards that:

The standard also informs consumers of what information they can expect from manufacturers and retailers

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Active implantable medical devices - Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers) Ingestion-build-258901 BS EN 12522-21 Scope This Part 2 1 specifies requirements that are applicable to those active implantable medical devices intended to treat bradyarrhythmias. 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 2 1 is also applicable to some non implantable parts and accessories of the devices (see Note 1). The characteristics of the implantable pulse generator or lead shall be

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