2024 Tüyap Fair

As UDEM Inc., with over twenty years of experience, we are positioned as one of the leading and pioneering organizations in the industry. Our company, which embraces quality, impartiality, and independence as indispensable values, provides conformity assessment services to medical device manufacturers under the Medical Devices Regulation (EU) 2017/745 as a Notified Body (Notified Body 2292).

Last week, we had the opportunity to participate in the Expomed Eurasia Fair held at the Tüyap Fair and Congress Center. At this event, which serves as a meeting point for medical product and medical device manufacturers, we had the opportunity to share information about conformity assessment and introduce our services to manufacturers seeking access to the European market as UDEM Inc.

Our goal is to provide quality and timely services to all medical device manufacturers in compliance with the current regulations, primarily in Turkey, as well as in the European Union and globally. In this regard, we have expanded our expert team and completed comprehensive training programs.

Until the official deadline for the transition to the Medical Devices Regulation (MDR) on May 26, 2024, all medical device manufacturers can contact us via email (mdr@udem.com.tr) or phone to obtain information and/or apply for MDR conformity assessment processes.

As part of the Medical Device sector, we hope for the industry to achieve many successful organizations and contribute to the health of our country and the world.