SPM-D is a device for testing pulmonary function, combining with professional pulmonary function software, it is used to test the patient's respiratory function and lung status; it adopts differential pressure collection principle to measure FVC, SVC, MVV, MV and relative parameters, real-time displays respiratory waveform, which is applicable for diagnosis and response evaluation of lung diseases such as asthma, COPD, pulmonary fibrosis and cough, etc. , preoperative safety evaluation and routine physical examination, etc.
It can be widely used in many scenarios, such as respiratory medicine, thoracic, anesthesiology, surgery, prevention and control institutions of occupational disease, physical examination institutions, etc. 1Measure and display over 100 parameters related to FVC, SVC, MVV and MV functions. 2Display trend chart and respiratory waveform tested, recommend the optimal test curve intelligently. 3With management functions of user information and case data. 4Built-in multiple predicted values, which can be set manually.5BTPS self-correction function, measure environment parameters automatically. 8With calibration function and quality control, ensure the test accuracy. 9With quality control function, recommend the test curve with high acceptability intelligently.
10With report generation, editing and printing functions. Volume range: 0 10 L. Flow range: 0 L/s 16 L/s. Volume accuracy: ± 3 % or ± 0.05 L (whichever is greater).Flow accuracy: ± 5 % or ± 0.17 L/s (whichever is greater). Dimension: 143 mm (L) × 84 mm (W) × 41 mm (H). 1Collect the data by a differential pressure sensor, more accurate in results and more sensitive in response.
2Compact and portable in design, light in weight. 3Convenient to disassemble, easy to clean, disinfect and replace components. 4With multiple functions, and it can measure many parameters. 6With information indicator, which is used to indicate the operating status of the probe.ComIndex code:on the box. Food and Drug Administration and state and local regulatory agencies. The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE, TUV of Europe. The Fingertip Pulse Oximeter that is FDA 510K Approved. 100% satisfaction is our goal! We are looking forward to establishing a successful business relationship with you.
Only english user guide, if you need any other language, please contact me. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Spirometers & Peak Flow Meters".
The seller is "joywang011" and is located in this country: CN. This item can be shipped worldwide.