Medical devices of all classes, active implantable devices and procedure packs and kits sold in Italy to the Public Sector must be registered in an Italian database ("Repertorio"), administered by the Ministry of Health through its new system, NSIS. This requirement is a national regulation with no relation to the fact that the product might already be CE marked. Medes Limited is qualified and experienced in this registration and can carry out all the activities required to complete the process.

For immediate assistance with your product registration with the NSIS, please fill out the following form.  We offer a one week standard or an expedited overnight registration process.

For more information, please submit your inquiry or chose to consult our online experts right now.