Oxygen therapy hyperbaric chamber Omega

multiplace

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. Features Medical Device Quality Management Systems EN ISO 13485:2016 Modern Design TurnKey HBO Center Project Development Wide, Comfortable and Ergonomic Interior Design 3 Different Fire Supression Systems (EN16081, NFPA99) Sophisticated HiperSoft Software System (Customized Automation Option) Medical Device Addition Air Condition