Pressure Regulators and Flowmeters, all medical gases
The supply of all medical gases through measurement devices requires accuracy and experience in manufacturing and development, so we underline once more that all these devices are made in full compliance with European standards and technical regulations, as well as requirements of Regulation (EU) MDR 2017/745 and the approval criteria set by national and international certified bodies.
All regulators and flowmeters are rigorously tested, both in flow-meter™ own quality-assurance laboratories and by independent validated laboratories, to ensure that the products meet all the requirements of the medical applications in any foreseeable therapeutic condition.
The CE marking procedure is carried out according to the requirements of a complete EN ISO 13485 quality system.
In compliance with the New Guidelines of the Italian Ministry of Health of 28/03/2013 regarding health advertising concerning medical devices, in vitro medical diagnostic devices and medical surgical facilities, we caution that the information contained in this website is exclusively directed at professional practitioners. All contents are of an informational nature and do not have advertising purposes.