Possible Problems And How To Solve Them; Technical Specifications; Maintenance And Repairs; Ambient Conditions - Medel mebby NEBULBABY Manual De Instrucciones

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man NEBULBABY 13/22 uk
19-10-2004
UK

POSSIBLE PROBLEMS AND HOW TO SOLVE THEM

The device does not switch on:
1.
Make sure the plug is firmly fitted to the wall socket;
2.
Make sure that the device has been operating within operating limits indi-
cated in this instructions manual (30 min. ON/30 min. OFF).
The device does not nebulize, or it nebulizes very weakly:
1.
Make sure that the ends of the air tubing are fitted tightly onto the main
unit and onto the nebulizer;
2.
Check whether the nebulizer is empty from medication or full of an exces-
sive medication quantity (MAX. 5ml);
3.
Check whether the nebulizer nozzle is obstructed;
4.
Check whether the air conduction cone is inserted (pic. C).
Should the device not start working properly again, address to an authori-
zed technical service centre or to MEDEL CUSTOMER SERVICE.

MAINTENANCE AND REPAIRS

In case of failure, address to qualified personnel authorized by Medel S.p.A..
Never open the device. There are no user-serviceable parts within. The com-
pressor requires no lubrication or maintenance.
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18

TECHNICAL SPECIFICATIONS

Model:
Nebulbaby
Electricity supply:
see rating label on the device bottom
Nebulization rate:
0,23 ml/min.
Particle size:
MMAD 1,83 µm (NaCl 0,9%) - API AEROSIZER
MMD 4,27 µm - INSITEC MALVERN
Compressor max. pressure:
230 kPa (2,30 bar)
Weight:
1,5 kg
Size:
(H) 167 x (L) 145 x (P) 97 mm
Noise Level:
55 dBA
Class II Device (Double Safety Insulation).
Type B Device (device with specific protection against electrical hazards).
Device not protected against sprinkles.
Device not suitable for use in presence of anaesthetic substances inflammable
with air, oxygen or nitrogen protoxide.
Device not suitable for use in anaesthesia or lung ventilation systems.
Technical modifications reserved!
Reference to Standards:
Electric Safety Standards CEI EN 60601.1
Electromagnetic Compatibility according to
CEI EN 60601.1.2
Class IIa Medical Device according to
93/42/EEC "Medical Device" Directive.

AMBIENT CONDITIONS

Storage Condition
Temperature:
MIN -25°C-MAX 70°C
Humidity:
MIN 10%RH-MAX 95%RH
Operating Conditions
Temperature:
MIN 10°C-MAX 40°C
Humidity:
MIN 10%RH-MAX 95%RH
Altitude:
from 0 to 2000m above sea level
19
UK
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