Medical Device Class Class IIA
Sensor Technology Ultrasonic Flow Measurement
Flow Range 0-14 L/s
Maximum Volume Measured 10 L
Volume Accuracy 2.00 % or 50 mL, Whichever is greater
Dynamic Resistance at 14 L/s 120 Pa*s/L
Quality / Medical Devices / Electrical Safety Standard ISO 13485, ISO 26782, ISO 10993-1, ISO 14971, ISO 15223- 1, EN 60601-1, EN 60601-1-2, EN 60601-1-6, EN 60601-1-11
Test Modes Full Loop Test, Exhalation Only Test, SVC, MVV
Parameters FVC, FEV0.75, FEV1, FEV3, FEV6, FEV0.75/FVC,FEV1/FVC, FEV3/FVC, FEV6/FVC, PEF, MMEF, FEF25, FEF50, FEF75, FEF25-75, FIV1(L), FIVC(L), PIF (L/s),FIF25-75 (L/s), MET25-75(s), FEV0.75/FEV6 (%), FEV1/FEV6, FEF50/FVC, MMEF/FVC, FIV1/FIVC (%), R50 (FEF50/FIF50) (%), FET, BEV, VC(L), VCin, VCex, ERV (L), IRV (L), IC (L), VT(L), MVV (L/min), MVV6 (L/min), VT (L), MVVtime (s), RF (1/min)
Power Supply 2 x 1.5V AA Alkaline Batteries
Dimensions 150 x 77 x 42 mm
Weight (With batteries) 230 g
Wireless Connection BLE 4.2
Use Environment Office, Clinic, Occupational Health, Ambulance, Primary Care, Hospital
Mouthpiece Adaptable with Bacterial Filters SpiroWay Pro
Predicted Values Quanjer 2012 (GLI), NHANES III 1999 (Hankinson), ERS 1993 (ECS, EGKS, Quanjer), Crapo 1981, Knudson 1976
Interface Device iOS Tablets, Android Tablets, Windows 10 PC
Calibration No routine calibration required
Pre - Post Test Yes
Data Storage EHR Integration / Cloud system / Unlimited Patient Records
ATS Error Codes Complies With Latest 2019 Spirometry Standard Update
Lower Limits of Normal (LLN) & Zscore Implementation Yes
SDK / API Integration Yes