Product Specifications; Maximum Pressure - Gima 28102 Guía De Uso

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)
MODEL
POWER SUPPLY
ABSORBED POWER
FUSE

MAXIMUM PRESSURE

MAXIMUM FLOW (in the compressor)
OPERATING PRESSURE
OPERATIONAL FLOW
ATOMIZATION
MMAD (measured in accordance
with EN 13544-1)
GSD
WEIGHT
SIZE
MAXIMUM NOISE LEVEL
FUNCTIONING
MINIMUM NEBULIZER VOLUME LEVEL
MAXIMUM NEBULIZER VOLUME LEVEL
ENGLISH
Medical device Class IIa
Mistral
230V~ / 50Hz
170 VA
F 1 x 2A L 250V
250 kPa (2.5 Bar)
14 L/min
110 kPa (1.10 Bar)
5.0 L/min at 110 kPa
0.35 ml/min (with 4ml solution NaCl 0.9%)
2.44
2.87
1.10 Kg
130 (L) x 89 (H) x 146 (P) mm
60 dB (A)
Ton: 20min / Toff: 40min
2ml
6ml