RECOPS became mandatory on 15 June 2026, just over a month ago.
This is the new IT application that replaces the previous CCPS and RPS systems.
Key points about RECOPS:
- It makes it possible to register and identify the devices marketed in Spain, together with their instructions for use and labelling
- From 15 June, economic operators marketing devices in Spanish territory must submit the communication to RECOPS within a period of no more than six months from the notification of the device to Eudamed
- To submit the communication in RECOPS, the device must be notified and visible in the Eudamed database, since the device data will be downloaded from Eudamed
At MeDev Consulting we provide end-to-end management of all your regulatory procedures: registration in Eudamed, obtaining the AEMPS manufacturing licence and registration in RECOPS. Our specialised team ensures that your devices comply with the applicable requirements and are correctly communicated on the required platforms within the established deadlines, guaranteeing a fast, secure process free of administrative complications.