2023: The PulsePen instrument was certified according to the Medical Device Regulation (EU) 2017/745 - MDR and the ISO 13485 Quality Management System of DiaTecne s.r.l. was renewed. 2021 - 2022: The PulsePen Sync interface has been introduced, which allows synchronization with DAQ devices in case you want to set up a multi-parameter system. 2019 - 2020: The PulsePen Holder was released allowing for stable signals capture - operator-independent. New features were added to the software. Radio disturbances from other devices were virtually eliminated 2017 - 2018: The PulsePen software was further improved. Comparative studies with invasive method were carried out with excellent results 2016: The Quality Management System of DiaTecne s.r.l. was certified according to ISO 13485 Standard. Full Quality Assurance System Approval Certificate was obtained for the PulsePen system according to the Directive 93/42/EEC, Annex II 2015: The PulsePen wireless system was certified according to the Directive 93/42/EEC, Annex VI 2014: PulsePen and PulsePenLab software were enhanced with new functions 2013: Final PulsePen wireless device was implemented 2012: The PulsePen wireless prototype was unveiled for the first time during the Artery 12 meeting in Vienna 2011: Start of development of the PulsePen wireless system including software redesign 2010: First studies on rats in France with the PulsePenLab 2009: The PulsePenLab prototype was developed and tested in the laboratory 2006 - 2008: Many research studies were carried out using the PulsePen 2005: The first model of PulsePen device was introduced in the market 2004: DiaTecne was established in Milan - Italy. The founders of the Company started with their high valued knowledge of tonometry and design of electromedical equipment and focused the main activities towards the research field of tonometry and the development of dedicated hardware devices and software applications