Technical Specifications - EMS EMSER Nebuliser Compact IH 55 Instrucciones De Uso

Operation with mains part
The mains part must only be connected to the mains volt-
age that is specified on the type plate.
• Power supply: 100–240 V~; 50–60 Hz; 0.15 A
• Insert the mains part connector plug
(A) into the provided connector sock-
et (B) and fully insert the mains part
into a suitable socket.
Note
• Ensure that there is a mains socket close to the set-
up area.
• Arrange the mains cable so that no-one will trip over it.
• To disconnect the device from the mains after inhala-
tion, first switch the device off and then pull the mains
plug out of the socket.
• The batteries do not need to be removed during oper-
ation with the mains part.
• The mains part cannot be used for charging batteries.

11. Technical specifications

Model: Emser Nebuliser Compact
Type: IH 55
Dimensions
(L×W×H) 146 × 51 × 85 mm
Weight 228 g incl. batteries
Battery-operated 4 × 1.5 V type AA, Mignon (LR6)
Expected product
life cycle 5 years
Filling volume Max. 10 ml
Medication flow rate > 0.25 ml/min
Vibration frequency 100 kHz
Housing material ABS
Operating condi- Temperature: +10 °C to +40 °C
tions Relative humidity:
< 93% non-condensing
Atmospheric pressure:
860 to 1060 hPa
Storage and trans- Temperature: -20 °C to +70 °C
portation conditions Relative humidity:
< 93% non-condensing
Atmospheric pressure:
860 to 1060 hPa
The serial number is located on the device or in the bat-
tery compartment.
Subject to technical changes. Wearing parts are excluded
from the guarantee.
B
Particle size diagram
A
Measurements were performed using a sodium fluoride
solution with a "Next Generation Impactor" (NGI).
The diagram may therefore not be applicable to suspen-
sions or highly viscous medications. You can obtain more
detailed information from the manufacturer of your med-
ication.
If the device is not used according to the instructions
specified, perfect functionality cannot be guaranteed! We
reserve the right to make technical changes to improve
and develop the product.
This device and its accessories comply with the Euro-
pean standards EN60601-1, EN60601-1-2 (In accord-
ance with IEC61000-3-2, IEC61000-3-3, IEC61000-4-2,
IEC61000-4-3,
IEC61000-4-6, IEC61000-4-11) and EN13544-1 and are
subject to particular precautions with regard to electro-
magnetic compatibility. This device meets the require-
ments of European Directive 93/42/EEC for medical devic-
es, as well as those of the Medizinproduktegesetz (German
Medical Devices Act).
21
Note
IEC61000-4-4,
Notes on electromagnetic compatibility
IEC61000-4-5,