TUR-MED HASTANE MALZ. SAN. TIC. LTD. ŞTI.

Tur-Med primarily manufactures basic electric hospital beds, including variations like single-motor, dual-motor, four-motor, and intensive care unit beds with five-column motors. Their portfolio also includes folding and hydraulic stretchers, motorised and wooden examination tables, and a home-type folding wheelchair with a commode attachment. Additionally, they produce a tissue specimen x-ray system, which is classified as an in vitro diagnostic (IVD) device.

Tur-Med is based in Turkey, which means its devices must comply with EU regulations if marketed in the European Economic Area. Since all listed devices fall under EU Class I classification, they are subject to basic requirements under EU MDR (Medical Device Regulation). The company registers its devices in euDaMed, the EU’s public registry for medical devices, to demonstrate compliance and traceability.

Tur-Med’s devices are listed in euDaMed, the official EU database for medical devices. This registry is critical because it ensures transparency and traceability of devices marketed in the European Union. Listing in euDaMed confirms that the manufacturer has provided necessary information about their devices, including classification, intended purpose, and compliance with EU regulations, which helps healthcare professionals and authorities verify legitimacy.

All of Tur-Med’s listed devices fall under EU Class I classification, which is the lowest risk category for medical devices. This classification means they pose minimal risk to patients and users, so they are subject to basic safety and performance requirements but do not require additional conformity assessments like clinical evaluations or third-party audits. However, even Class I devices must still comply with general safety principles and be properly labeled for their intended use.