I don't think that your product falls under category specific installation. These usually apply to large fixed installation which can't be easily moved to other location. In your case you first have to determine if your product falls under product specific standards (i.e. medical device directive , If not then your product falls under the EMC directive and in that case EN61000 is applicable. Your product has to pass emission (radiated and conducted) and immunity (radiated, EFT, ESD, Surge, voltage dips etc etc) tests. The cable length also determines which tests are applicable or not! In Europe EMC is based on self certification i.e. you need only to perform the EMC tests/measurements at a certified lab. The report is then sufficient proof that your product meets the EMC directive