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Vitalograph copd-6 usb

Vitalograph copd-6 USB

For copd screening compatible with Vitalograph Reports Software

The copd-6 usb identifies those at risk of copd at the pre-symptomatic stage to allow early medical intervention and facilitate better clinical outcomes.

This pioneering device screens out those whose FEV1 is normal, and who therefore do not have copd,without the risk of false copd negatives.

By linking to your PC the copd-6 usb produces electronic & hard copy reports.

Virtual Demonstration

  • Predicted values, 3 test results, best test, % predicted and lung age automatically tabulated
  • Obstructive index, copd (GOLD) Classification indicator
  • BMI calculated
  • Blow quality indicator
  • Interpretation of results
  • Interpretation of results

Reports include:

  • Single page record for screening or monitoring
  • Various report options
  • Optional subject ID and name fields (weight field optional)
  • Ability to add comments to the report
  • Age, height, gender, device ID, time/date fields automatically populated
  • Can automatically name the PDF file
  • Ability to add comments to the report

Vitalograph copd-6 USB

Technical Data
Product Vitalograph copd-6 USB
Model Number 4000
Part Number 40200, 40450, 40350, 40850
Description Vitalograph copd-6, Vitalograph copd-6 usb, Vitalograph copd-6 bluetooth, Vitalograph copd-6 serial
Parameters Displayed FEV1/FEV6/ratio and % predicted
Quality of Blow Indicator Yes
Obstructive Index Mild, Moderate, Severe (FEV1% predicted)
copd Classification Normal (not copd); Stage I, II, III & IV (FEV1% predicted)
Lung Age Indicator Yes
Flow Impedance Better than 0.15 kPa/L/s at 14 L/s
Operating Temperature Range 17 - 37°C
Sensor Stator rotor
Accuracy Better than +/- 3%
Range 0 - 9.99 L BTPS
Size 113 x 63 x 48mm
Weight 55g net
Display Custom Liquid Crystal Display
Power AAA batteries
Performance Standards ISO 26782:2009
ISO 23747:2007
ATS/ERS 2005
Safety Standards IEC 60601-1:2005
Medical Safety Standard Medical Devices 93/42/EEC (as amended)
Designed and manufactured to following QA/GMP standards ISO 13485:2003
FDA 21CFR820