17
introduce any solution and do not inhale. Contact the technical service, specifying the
methods of use and the type of drug used.
17. Remember to:
- use this appliance only with medicines prescribed by your doctor;
- perform the treatment by using only the accessory instructed by your doctor accord-
ing to the disease.
Under certain fault conditions, the packaging temperature can raise and there might
be risk of burns if the user comes into contact with such parts. In any event, the temper-
atures do not exceed the limit of 105°C [221°F] (ref. Interpretation Sheet IEC 60601-1).
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
Mistral
POWER SUPPLY
230V~ / 50Hz
ABSORBED POWER
170 VA
FUSE
F 1 x 2A L 250V
MAXIMUM PRESSURE
250 kPa (2.5 Bar)
MAXIMUM FLOW (in the compressor)
14 L/min
OPERATING PRESSURE
110 kPa (1.10 Bar)
OPERATIONAL FLOW
5.0 L/min at 110 kPa
ATOMIZATION
0.35 ml/min (with 4ml solution NaCl 0.9%)
MMAD (measured in accordance
with EN 13544-1)
2.44
GSD
2.87
WEIGHT
1.10 Kg
SIZE
130 (L) x 89 (H) x 146 (P) mm
MAXIMUM NOISE LEVEL
60 dB (A)
FUNCTIONING
Ton: 20min / Toff: 40min
MINIMUM NEBULIZER VOLUME LEVEL
2ml
MAXIMUM NEBULIZER VOLUME LEVEL 6ml
ENGLISH
