Specifically, the request signed by Eng. Vanessa Biavati concerns the update of certain designation codes in order to reduce the limitations previously in place:
- Code MDA 0306: only active devices for extracorporeal circulation are formally excluded
- Code MDA 0313: only active non-implantable prostheses are excluded
- Code MDA 0317: expansion to all active non-implantable devices and to devices for cleaning, disinfection, and sterilization (including moist heat and dry heat sterilizers).
This monitoring activity ensures that ECM’s scope of designation is always accurately reflected at an international level, providing operational certainty to our industrial partners.
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30 Jun 2026
UPDATED THE LIST OF FAKE/FORGED DOCUMENTS
ECM – Ente Certificazione Macchine is informed of the existence of fakes/counterfeit certificates/laboratory test reports/other ECM documents relating to certain European Directives or International Standards. No one has permission to issue certificates or other documents in our name and on our behalf, so ECM will take action against any companies that issue certificates/documents without authorization.
25 Jun 2026
UPDATED LIST OF IMPROPER USES OF THE NAME ENTE CERTIFICAZIONE MACCHINE SRL AND/OR THE ECM NUMBER OF NOTIFIED BODY 1282
To consult the updated list of reports of misuse of the name Ente Certificazione Macchine srl and/or the notified body number 1282, click here.
22 Jun 2026
The voices of the Memorandum of Understanding (MoU) with the Korea Total Healthcare Ecosystem Association (KoTHEA): Gianluca Baldoni – Internationalization of the regional production system (Emilia-Romagna Region)
As part of the signing of the Memorandum of Understanding (MoU) on May 15, 2026, between ECM – Ente Certificazione Macchine and KoTHEA (Korea Total Healthcare Ecosystem Association), we continue to gather testimonials from the institutions and key partners supporting this important strategic bridge between Italy and South Korea. Today we feature the contribution of Dr. Gianluca Baldoni (Internationalization of the Regional Production System – Attractiveness, Internationalization, and Research Sector; Export and Trade Fair System Area of the Emilia-Romagna Region), who participated in the institutional event held in the presence of local authorities and the Consul General of the Republic of Korea in Milan.
19 Jun 2026
EUDAMED: The Regulatory Turning Point for Medical Devices
May 28, 2026, marked a watershed moment for medical devices in Europe. As of this date, full EUDAMED registration became mandatory for all devices undergoing certification under the MDR and IVDR regulations. The database becomes the operational hub of the single market. This is not a bureaucratic formality, but a binding requirement to maintain market access.
19 Jun 2026
The voices of the Memorandum of Understanding (MoU) with the Korea Total Healthcare Ecosystem Association (KoTHEA): Choi Taeho – Consul General of the Republic of Korea
International ties and strategic development prospects are strengthening around the crucial Memorandum of Understanding (MoU) signed at the Valsamoggia headquarters between the Korea Total Healthcare Ecosystem Association (KoTHEA) and the European notified body Ente Certificazione Macchine (ECM). The official ceremony was graced by the prestigious participation and institutional support of Choi Taeho, Consul General of the Republic of Korea, who emphasized the high political and economic value of this agreement. The agreement represents not only a technical milestone but also a genuine turning point in industrial and regulatory relations along the Seoul-Rome axis, fitting into a rapidly evolving global macroeconomic framework.
18 Jun 2026
New Machinery Regulation, the entry into force approaches: what’s new for Manufacturers
The European regulatory landscape is undergoing a crucial transformation with the introduction of Regulation (EU) 2023/1230, which will permanently phase out the historic Machinery Directive 2006/42/EC. One of the most impactful changes concerns the obligation to integrate cybersecurity as an essential element of product safety.
18 Jun 2026
IMPORTANT NOTICE: Immediate suspension of the use of the product “Hyperbaric chamber”
We would like to inform all our valued customers and business partners of an urgent measure that requires the utmost attention and timely cooperation from all users.