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Pressure regulators for medical devices
A pressure regulator is a device that lowers the outlet pressure to a safe level. It works by reducing the inlet pressure to reduce the outlet's pressure. There are several types of pressure regulators, but they all have similar uses. The type of use for a regulator will determine its size, weight, and port sizes. The design will also depend on its components. A pressure reducing element, such as a diaphragm, springs, or valve, will determine how much it weighs.
Generally, pressure regulators are designed to be fitted to refillable cylinders, whose working pressure is between 0.07 and 30000 kPa. The device can be equipped with flow controls and measurements. In addition, a pressure gauge is available to help the user set the desired pressure. A safety gauge will allow users to know how much air to add or remove at a time. This information is necessary to ensure patient safety and quality.
The safety of pressure regulators is critical. A regulator is designed to work safely. The valve itself is made of brass and has a membrane inside. This enables accurate setting of the outlet pressure. Each model includes a mechanical safety valve that prevents high-pressure gas from exiting the regulator. Additionally, each pressure-regulating device has sinter filters on the inlet for added safety. The valves on the regulators are designed to prevent any high-pressure gas from entering the system.
A pressure regulator is an important piece of equipment for medical professionals. It's essential for the safety of the patient. The device must meet the safety and effectiveness standards of ASTM G175-03 and special controls guidance. The manufacturer should consider this information carefully before implementing a product design. You can read more about pressure regulators on the FDA website. It's also helpful to understand the history of the device to ensure its safety. In addition to safety, it may also improve the quality of life.
The FDA has also proposed to reclassify pressure regulators that are used with medical oxygen as class II medical devices. The devices are already classified as class II medical devices. In addition to the safety requirements, the FDA has received reports of adverse events involving oxygen pressure regulators. Some of these incidents were so severe that they injured emergency medical personnel and patients. Hence, the safety standards are necessary. The NFPA safety guidelines are an important part of healthcare and are intended to protect patients.
Its design is compact, silent, and energy-saving. It's compatible with most medical gases, and features a piezo ceramic construction that is easy to clean. The piezo valves are also energy-efficient, and they do not produce heat. They can be used in any temperature and for any application. This is an important consideration for any medical application. If you're a healthcare professional, pressure regulators should be approved by the FDA.