Victoris Health Tıbbi Cihazlar AŞ

Victoris Health Tıbbi Cihazlar AŞ specializes in reusable medical devices for central sterile services departments (CSSD). Their portfolio includes instrument trays and sterilization container systems, such as filters and accessories designed to support sterilization processes in healthcare environments. These products are engineered to improve efficiency and safety in sterilization workflows.

Victoris Health Tıbbi Cihazlar AŞ is headquartered in Turkey, which means its devices must comply with EU medical device regulations if marketed in the European Economic Area. Since their products fall under EU Class I classification, they are subject to mandatory registration in EUDAMED, the EU’s medical device registry, to ensure traceability and transparency for regulatory oversight.

Yes, Victoris Health’s devices are listed in EUDAMED, the European database for medical devices. This registry is critical because it provides public access to device information, including manufacturer details, device identification, and regulatory status. Listing in EUDAMED ensures compliance with EU requirements and allows healthcare professionals, regulators, and patients to verify the legitimacy and traceability of the company’s products.

Victoris Health’s sterilization container systems and accessories are classified as EU Class I medical devices. This classification is determined by their intended purpose—supporting sterilization processes without invasive or high-risk procedures. Class I devices typically pose the lowest risk to patients and users, requiring mandatory registration in EUDAMED but not additional conformity assessments beyond basic manufacturing controls.