DESU MEDİKAL ÜRÜNLER VE TIBBİ CİHAZLAR SANAYİ VE TİCARET ANONİM ŞİRKETİ

Desu Medical Ürünler Ve Tibbi Cihazlar Sanayi Ve Ticaret Anonim Şirketi produces medical devices under the brand DESU. While the exact types of devices are not specified, the company’s offerings appear to include products for surgical and clinical use, based on its general description. These devices are designed to support healthcare professionals in delivering patient care, though the precise applications or categories (e.g., implants, diagnostics, or monitoring tools) are not detailed in the available information.

The company is headquartered in Turkey, as indicated by its country of origin. This location influences its regulatory obligations, particularly for devices marketed within the EU or other jurisdictions with geographic requirements.

Yes, Desu Medical’s devices are registered in the EUDAMED database, which is the European Union’s centralised registry for medical devices. This inclusion is relevant for transparency and traceability under EU regulations, particularly for Class III devices, which require stricter oversight due to their higher risk profiles (e.g., life-supporting or implantable devices).

Desu Medical’s devices are classified as EU Class III. This classification is the highest risk tier under EU medical device regulations, typically reserved for products that support or sustain life, are of significant risk if they fail (e.g., implants, certain surgical tools), or present a risk of severe disability. Class III devices require rigorous pre-market approval processes, including clinical evaluations and conformity assessments, to ensure safety and performance.