| Product | In2itive Handheld Spirometer |
| Model Number | 2120 |
| Subjects | Automatic population of database from Spirotrac. Name, ID; Age, Height, Gender; Smoking status, Body Mass Index and more depending on model. Storage of up to 10,000 subjects |
| Environmental Data | Selectable: Temperature (built in sensors), Barometric pressure, altitude, humidity |
| Test types | Single breath tests, flow/volume loops, multi-breath testing, tidal breathing and combined VC/FVC type test methods supported |
| Selectable Parameters (depending on model) | VC; IVC; IC; VT (TV); TLC; RV; IRV; ERV; FRC; FVC; FIVC; FEV1; FEV3; FEV6; FVC; FEV1/VC; FEV1/FVC; FEV3/VC; FEV3/FVC; FEV1/FEV6; FEF75; FEF50; FEF25; FEF25-75; FEF25-75/FVC; FIV1; PIF, FIV1/FIVC, FIF25, FIF50, FIF75, FEF50/FIF50, FET, MVVind, FEV1 Ratio; FEV0.5; PEF L/min; PEF L/s; FEF 0.2-1.2; FEF 75-85%; FEF25%; FEF50%; FEF75%; FMFT; FIF25%; FIF50%; FIF75%; PIF; FEV0.75; Lung Age and more |
| Predicted Values Selectable (depending on model) | ERS/ECCS; NHANES, Polgar, Pereira, Berglund, Forsche, Gutierrez, Hedenström, Taiwan; Knudson, Crapo; Hsu; KNLW; Viljanen; SEPAR; Gulsvik; SBPT; Tamura; Ip; Quanjer; Wang; Dockery and more |
| Suggested Interpretation | User selectable |
| Flow Technology | Fleisch Pneumotachograph (No3 size) |
| Resolution | 10 mL volume; 0.01 L/s flow |
| Data Storage | Stores up to 10,000 subjects and hundreds of test sessions |
| Accuracy when in Operating Range | Volumes: Better than ± 3% (Max 10L / Min 0L); Flows: Better than ± 10% (Max 16L/s / Min 0.02L/s); Linearity: ± 5% in range 0.1 L/s to 16 L/s PowerSAFE: Input 100 - 240V AC 50-60Hz, output 5V DC |
| Battery Pack | Rechargeable Lithium Polymer 3.7v 2000mAH |
| Dimensions | Device: 160mm x 100mm x 45mm (with flowhead attached) |
| Net Weight | Device: 230g |
| Gross Weight and Size (Packed) | Weight: 1.5kg, Packed Size: 213mm x 199mm x 158mm |
| Storage Humidity | 10% to 95% |
| Storage Temperature | 0°C to 50°C |
| Recommended Operating Temperature Range | 17 to 37°C; Design Limits 10-40°C |
| Ambient Humidity | 0% to 99% |
| Connectivity | USB 2 |
| Max Test Duration | 20s FVC; 30s VC |
| Performance Standards | ISO 26782:2009 ISO 23747:2007 ATS/ERS 2005 |
| Safety Standards | IEC 60601-1:2005 |
| Medical Safety Standard | Medical Devices Directive 2007/47/EC |
| Designed & Manufactured Under | ISO 13485:2003 FDA 21CFR820 CMDR |