The production of medical devices is a sector that is strictly subject to numerous regulations that prescribe unavoidable product requirements. The aim is to ensure the production and placing on the market of medical devices that are safe and fit for their intended purpose. RI.MOS. is certified according to the ISO 13485 standard, which is the most effective and authoritative way to meet all the quality requirements of a medical device manufacturing system. ISO 13485 is an internationally recognised standard which, although voluntary, is required by national legislation in many countries as part of the approval and market introduction process for devices.
RI.MOS. is also very careful to meet the requirements defined by the regulations in force at European level, in particular DIR 93/42/EEC and EU REG. 2017/745. This activity guarantees the protection of the safety of patients and healthcare professionals and the quality of its products.
