17
Gima S.p.A. cannot be held liable for accidental or indirect damage resulting
from alterations of the device, repairs and/or unauthorized technical interventions, or
damage to any of its part due to accident, misuse and/or abuse.
Any unauthorized intervention on the device, even the slightest one, will imme-
diately invalidate the warranty and does not ensure the compliance with the techni-
cal and safety requirements provided by Directive MDD 93/42/EEC (and subsequent
amendments) and by the related reference standards.
PRODUCT SPECIFICATIONS
TYPE (Directive 93/42/EEC)
Medical device Class IIa
MODEL
Corsia
POWER SUPPLY
230V~ / 50Hz
ABSORBED POWER
170 VA
FUSE
F 1 x 1.6A L 250V
MAXIMUM PRESSURE
250 kPa (2.5 Bar)
MAXIMUM FLOW (in the compressor)
16 l/min
OPERATING PRESSURE
130 kPa (1.30 Bar)
OPERATIONAL FLOW
5.2 l/min a 130 kPa
ATOMIZATION
0.50 ml/min (with 4ml solution NaCl 0.9%)
MMAD (measured in accordance
with EN 13544-1)
3.25
GSD
3.45
WEIGHT
2.20 Kg
SIZE
255 x 190 x 165 (h) mm
MAXIMUM NOISE LEVEL
~ 57 dB (A)
FUNCTIONING
Continuous
MINIMUM NEBULIZER VOLUME LEVEL
2ml
MAXIMUM NEBULIZER VOLUME LEVEL 6ml
OPERATING CONDITIONS
Room temperature: 10 ÷ 40°C
Percentage of humidity in the environment:
20 ÷ 85% RH
Atmospheric pressure: 800 ÷ 1060 hPa
Altitude: 0 ÷ 2000m above s.l.
STORAGE AND TRANSPORT
CONDITIONS
Room temperature: -25÷ 70°C
Percentage of humidity in the environment:
10 ÷ 95% RH
Atmospheric pressure: 500 ÷ 1060 hPa
ENGLISH
