Our response is that it applies to all hearing loop system products (existing and new products) but we understand there is a transitional 12 months until 13 June 2017 in which equipment complying with the older R&TTE Directive can be placed on the market. We are waiting for official confirmation of this.
Our response was that the equipment had been incorrectly described by the shippers and that exports to the USA should be careful about the wording used and to avoid the SIV designation ‘assistive medical devices’. One suggestion from a member experienced with US importing is to use the description ‘communications equipment’. We also now have […]