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Multiplace Omega Chamber

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.

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Medical Device Quality Management Systems EN ISO 13485:2016

Modern Design

TurnKey HBO Center Project Development

Wide, Comfortable and Ergonomic Interior Design

3 Phased Fire Supression Systems (EN16081, NFPA99)

Sophisticated HiperSoft Software System (Customized Automation Option)

Medical Device Addition

Air Condition

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