Operating Conditions
Applied norms
Humidity: MIN 10% RH; MAX 95%RH
Temperature: MIN + 10 °C, MAX + 40 °C
Humidity: MIN 10% RH, MAX 95%RH
Electrical Safety Standard EN 60601
Electro Magnetic Compatibility EN 60601
About 10 years.
Life expectancy
Storing of parameters, Flow/Volume and Volume/time curves. The number of tests cannot be precisely defined as it depends on the set up made by the individual user.
Display:
spirolab
III B/W: Graphic LCD passive type FSTN 320x240 Pixel
spirolab
III colour: Graphic LCD 16 colour passive type FSTN 320x240 Pixel
Keyboard:
Silicon rubber keyboard
07 Hardware function keys, with symbols
15 Software function keys, with symbols
05 Arrow keys with symbols (right, left, up, down, enter)
02 Gender identification with appropriate symbols
10 Number keys
29 International alphabet keys.
WARNING
This device is a Class IIa medical device, according to the European Directive
93/42/EEC, annez IX, rule 10.
1.6
TECHNICAL SPECIFICATIONS
1.6.1 Features of the spirometer
Measured parameters:
SYMBOL
*FVC
*FEV1
*PEF
Best FVC
Best FEV1
Best PEF
*FEV1/FVC Best FEV1/FVC
FVC
FEV1
FEV1/FVC
FEV1/VC
PEF
FEF2575
FEF25
FEF50
DESCRIPTION
Forced Vital Capacity
Volume expired in the 1 st
second of the test
FEV1/FVC x 100
FEV1 / best between EVC and IVC x 100
Peak expiratory flow
Average flow between 25% and 75% of the FVC
Forced Expiratory Flow at 25% of FVC
Forced Expiratory Flow at 50% of FVC
L
L
%
%
L
L
L/s
L/s
L/s
L/s
L/s
Units
spirolab
III – User Manual Code MIR 980067 REV 2.0 Page 17 / 74
