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Vitalograph Lung Monitor USB Respiratory Monitor
For the home monitoring of FEV1, FEV6 & the ratio with electronic & hard copy reports
The lung monitor USB combines all of the features of the lung monitor with the ability to link to your PC. Session data and device ID may be transmitted to Vitalograph Reports or an API developers' kit is available for providers of e-Diary, home hub and telemedicine solutions.
Features:
- BMI calculated
- Blow quality and number of blows indicated
- Ability to add comments to the report
- Information presented in tabular and graphical form
- Report headers can be customised
- Automatically names the pdf file using subject name and date
Reports include:
- Subject ID and name
- Age, height, gender, and weight fields optional
- Best FEV1, FEV6 and ratio automatically populated
- Personal best FEV1 set in the lung monitor
- Device ID and time/date fields
- Automatically populated
Technical Specification
Brand - Vitalograph
Detailed Technical Information -
Product | Vitalograph lung monitor usb |
Model Number | 4000 |
Part Number | 40500, 40400, 40750, 40950 |
Description | Vitalograph lung monitor, Vitalograph lung monitor usb, Vitalograph lung monitor bluetooth, Vitalograph lung monitor serial |
Parameters Displayed | FEV1, FEV6 , FEV1/FEV6 ratio and FEF |
Memory | FEV1, FEV6 , FEV1/FEV6 ratio and FEF |
Quality of Blow Indicator | Yes |
Accuracy | Better than +/- 3% |
Range | 0 - 9.99 L BTPS |
Sensor | Stator rotor |
Flow Impedance | Better than 0.15 kPa/L/s at 14 L/s |
Power Supply | AAA batteries |
Display | Custom liquid crystal display |
Size | 113 x 63 x 48mm |
Weight | 55g net |
Performance standards | ISO 26782:2009 ISO 23747:2007 ATS/ERS Guidelines 2005 |
Operating Temperature Range | 17 - 37°C |
Management Zones | Factory set 3 zones Green/Yellow threshold 95% Yellow/Red threshold 90% Zones may be changed by the user And number of zones increased to 4 |
Safety Standards | IEC 60601-1:2005 |
Medical Safety Standard | Medical Devices Directive 93/42/EEC |
Designed and manufactured to following QA/GMP standards | ISO 13485:2003 FDA 21CFR820 CMDR |