Healthshine Oxygen Bullnose Flow Regulator Full Set

The Healthshine Oxygen Bullnose Flow Regulator Full Set is engineered to precisely manage oxygen delivery from high-pressure cylinders to patients. This essential medical device functions by reducing the high pressure of oxygen from a cylinder to safe, usable levels for medical oxygen therapy. It is designed to regulate the flow rate from an oxygen supply system, ensuring consistent and stable oxygen output for various clinical applications.

This regulator features a maximum inlet pressure of 3000 psi and delivers a controlled outlet pressure of 50 psi, facilitating accurate oxygen administration. For enhanced patient and user safety, the unit incorporates an integrated safety relief valve designed to release pressure if it reaches dangerous levels within the oxygen tank. A calibrated pressure gauge provides precise readings of the oxygen tank's contents, allowing for effective monitoring. Additionally, a metal filter at the inlet connection helps restrict dust from entering the system, contributing to cleaner oxygen delivery.

The Healthshine Oxygen Bullnose Flow Regulator Full Set is equipped with a bullnose fitting, ensuring a secure and leak-free connection to standard oxygen cylinders. It also includes a connection port for the quick attachment and detachment of auxiliary medical devices. As a medical gas pressure regulator, this device is classified by the FDA as a Class I medical device, with exemptions from premarket notification requirements when conforming to recognized standards such as ASTM G175-03.

Key Features : 

Enables precise pressure reduction and controlled oxygen delivery from high-pressure cylinders for medical therapy.
Manages oxygen flow rates to ensure consistent and stable output for patient administration.
Incorporates integrated safety features, including a safety relief valve and a calibrated pressure gauge, for secure operation.
Designed with a bullnose fitting for reliable connection to standard oxygen cylinders and a port for auxiliary device integration.
Classified as an FDA Class I medical device, adhering to established regulatory guidelines.