ABOUT US

OKUMAN Medical Systems started its commercial life in 2010 in Ankara on sleep and respiratory disorders. It became the fastest growing home care company in our country with its trained and experienced sales, marketing, clinical support and technical service personnel. OKUMAN is among the biggest companies in Turkey about Sleep Diagnostic and Therapy Devices, Operating Room, Intensive Care, Neonatology and Cardiology. OKUMAN manufactures the first design and production of many medical devices in our country, especially Anesthesia Devices, Baby Incubators and Phototherapy Devices in its factory located in Ivedik Organize Sanayi Bolgesi with ISO 9001, ISO 13485, CE and Domestic Manufacturing Certificates. In addition to its own products, OKUMAN is a distributor of the PMLS product group of NDD, MEC, Enmind and Mindray. OKUMAN has accomplished many hospital projects in Turkey and abroad with its CE and TSE quality certified products, successfully completed the installation of the products in the hospital, and performed After Sales and Technical Services. OKUMAN MEDIKAL SISTEMLER A.S. is a Turkey distributor which are the world leader in its field and the most respected brands, and brings their products to consumers at our country and abroad.

OUR QUALITY POLICY

At Okuman Medikal, we are committed to acting in full compliance with national and international regulations, particularly the European Union Medical Device Regulation (MDR 2017/745), and all other relevant regulatory requirements. Our approach is based on the health and safety of individuals, patient and user safety, employee safety, and environmental sensitivity. In line with the ISO 13485 and ISO 9001 quality management system standards, we are dedicated to providing safe, performance-validated products that meet the applicable requirements, continuously improving the effectiveness of our quality management system, and systematically meeting customer expectations.

Within this framework, we plan, implement, and ensure the continuity of risk management, clinical evaluation, traceability, post-market surveillance (PMS), and vigilance processes integrated into our quality management system. We regularly monitor, measure, and improve process performance with our competent human resources and effective supplier management.

In accordance with this policy, we are committed to:

• Ensuring sustainable compliance with regulations, standards, and regulatory requirements,
• Managing product safety and performance with a risk-based approach,
• Monitoring, analyzing customer feedback, and turning the results into improvement actions,
• Measuring process performance and maintaining a data-driven continuous improvement culture at the corporate level,
• Managing the supply chain based on evaluation, monitoring, and development principles,
• Supporting competence, training, and employee engagement to strengthen quality awareness and culture.