Active implantable medical devices - Particular requirements for cochlear and auditory brainstem implant systems1 Scope This Part 2 3 of EN 45502 specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing impairment via electrical stimulation of the auditory pathways. Devices which treat hearing impairment via means other than electrical stimulation are not covered by this European Standard. The tests that are specified in EN 45502 are type tests and are to be carried out on samples of a device to

BS EN ISO 8130-1 is the first part of the BS EN 8130 multi-series on coating powders

– Measurement

the technical information

The Chartered Institute for the Management of Sport and Physical Activity

ISO/IEC 15693‑3 specifies protocols and commands

increase the efficiency of the project

Contents of BS EN 61000-4-14:

and can also be used to propel vehicles

users will be able to use paper machines safely without any harm

Appliances specifically intended for use under medical supervision (IEC 60601-2-35)

Test procedures used to support the test methods in BS EN 12697-30 to BS EN 12697-33

which are used in ISO/IEC 11179