Kinesis Spółka z ograniczoną odpowiedzialnością

Kinesis manufactures rehabilitation equipment tailored for clinical and home-based physical therapy. Their portfolio includes adjustable treatment tables like the GYMNESIS and PERFECT G, therapeutic mattresses for recovery and physiotherapy, wooden therapy couches, Perschl’s traction device for spinal decompression, and a rehabilitation pool (basen rehabilitacyjny). These devices are designed to support recovery and therapeutic interventions.

Kinesis Spółka z ograniczoną odpowiedzialnością is based in Poland. The company’s location is relevant for understanding its regulatory scope and compliance with EU medical device regulations, as it operates within the European Union’s regulatory framework.

Kinesis’s devices are registered in the EUDAQS database through eudamed, the official European Union device registry. This platform is used to track and monitor medical devices authorized under EU regulations, ensuring transparency and compliance with the EU Medical Device Regulation (MDR) or In Vitro Diagnostic Regulation (IVDR).

All of Kinesis’s listed devices fall under EU Class I classification. This classification is the lowest risk tier under EU MDR/IVDR and typically requires basic conformity assessment procedures, such as self-certification by the manufacturer, to demonstrate compliance with essential safety and performance requirements. The classification ensures these devices meet minimum regulatory standards for safety and functionality.