What kinds of medical devices does VOSS VİTALİS work on?
Our scope covers diagnostic, treatment and monitoring devices, laboratory devices and kits, medical consumables, prostheses, orthoses and implants, and wearable health devices.
We design, develop, manufacture and distribute medical and biomedical products, building an integrated structure that also covers maintenance, repair and technical service.
In medical devices we handle the whole life cycle of a product within one structure: defining the clinical need, design and prototyping, pilot production, serial production and market launch. After-sales maintenance, repair and technical service are part of the same cycle.
Medical devices are tightly regulated in Türkiye and in international markets. The EU Medical Device Regulation (MDR 2017/745) applies in the European Union, and Türkiye applies a harmonised Medical Device Regulation. We develop our products against these frameworks and quality management standards such as ISO 13485.
Our scope covers diagnostic, treatment and monitoring devices, laboratory devices and kits, medical consumables, prostheses, orthoses and implants, and wearable health devices.
No. No product that requires a permit, registration or certification is placed on the market before those processes are complete. This rule applies to all of our business areas.
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