Vitalograph 40200 Electronic COPD Screener COPD-6

40200 Vitalograph Electronic COPD (Chronic Obstructive Pulmonary Disease) Screener COPD-6 The Vitalograph copd-6 is designed for rapid screening of at-risk groups to assess whether full spirometry is appropriate.

Vitalograph COPD (Chronic Obstructive Pulmonary Disease) screener provides classification of COPD, the stage of the disease and information on the degree of the obstruction clearly and simply.

Features:

• The Vitalograph copd-6 measures FEV1 and FEV6 and gives the FEV1% of predicted.
• Identifies those at risk of COPD at the pre-symptomatic stage to allow early medical intervention and facilitate better clinical outcomes
• Screens out those who’s FEV1 is normal, who therefore do not have COPD,without the risk of false negatives
• Diagnostic spirometry resources can be focused on those most likely to be diagnosed with COPD
• Displays the key parameters for clinical interpretation including obstructive index and COPD classification (stage I - IV)
• Displays FEV1, FEV6, ratio and % predicted, obstructive index, COPD classification and lung age
• Detachable flowhead makes cleaning simple
• Easy to use by non-respiratory specialists
• Built-in quality of blow indicator
• Designed for multi-subject use
• Large, easy to read display

Technical Data:

• Size: 100 x 65 x 32mm
• Weight: 55g net
• Displays: FEV1 and % Predicted , FEV6 and % Predicted, Ratio and % Predicted, Degree of obstruction, COPD Classification 
• Operating Temperature Range: 17 - 37° C
• Flow Detection Principle: Stator/rotor mass flow meter
• Volume Detection: Mass flow count
• Accuracy when operated in operating temperature range conditions:
• Better than +/- 3%
• Maximum Displayed Volume: 9.99 Litres
• Maximum Test Duration: 30 seconds
• Display: LCD
• Battery Type: AAA
• Battery Operating Life: 6 months typical
• Performance Standards: ATS/ERS :2005 Guidelines All COPD Guidelines 
• Safety Standards: EN60601-1-2, EN13826:2003
• Designed and manufactured to following QA/GMP standards: CE 0086, ISO 13485:2003, FDA 21CFR820