Safety is Hipertech’s top priority. As a medical device producer, Hipertech follows European and Global regulations, for instance, CE-Mark is approved by commercial associations under the norms of Medical Devices regulations: EN14931, 93/42/EEC, 2017/745 MDR (EU), ASME PVHO, Pressure Equipment Directive PED/2014/68/EU standards. With its modern project management approach, HBOT technology research and development and advanced production technologies implementation; Hipertech Ltd. designs and creates the latest technology Multiplace Omega Hyperbaric Chambers.

Hipertech has developed Quadro Chambers, featuring spacious, rectangular rooms designed for patient care, known as Quadro Care. These chambers incorporate all the features and conditions found in both Omega and Circular Chambers, while adhering to all relevant Medical Devices regulations. These regulations include EN14931, 93/42/EEC, 2017/745 MDR (EU), ASME PVHO, the Pressure Equipment Directive PED/2014/68/EU, and the standards required for the CE Mark.

Hipertech produces full and semi-acrylic Monoplace Chambers designed according to ASME PVHO and EN14931, 93/42/EEC, 2017/745 MDR (EU), EN ISO 13485:2016, Pressure Equipment Directive PED/2014/68/EU and the CE Mark standards. With their wide interior design and safety precautions, Our Monoplace Chambers comply all global standards for your medical centers with high-end technology.