Active implantable medical devices - Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators) Ingestion-build-146508 either totally or partially

either totally or partially

The relevant test method and launch condition should be chosen according to the type of fibre

Other materials also include waste

and samples of waste silk and uncrimped staple fibres having a fibre length of approximately 50 mm

BS EN 13311-5 aids the equipment manufacturer in the classification of kill tanks for the safe performance in biotechnological processes

Active implantable medical devices - Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators) Ingestion-build-146508 either totally or partially1 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