English En - Philips InnoSpire Go Manual

Cumulative drug deposition – Salbutamol
100.0
90.0
80.0
70.0
60.0
50.0
40.0
30.0
20.0
10.0
0.0
0.1 1
Upper aerodynamic diameter (µm)
Performance information provided as required by EN 13544-1:2007 may not apply for medications in
suspension or high viscosity form. In such cases information should be sought from the medication supplier.
Performance may vary based on atmospheric pressure depending on altitude above sea level, barometric
pressure, and temperature.
Nebulizer performances are based upon testing that utilizes adult ventilatory patterns and are likely to be
different from those stated for pediatric infant populations.
Electromagnetic information: The InnoSpire Go needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided in this document. Portable and
mobile RF communications equipment can affect medical electrical equipment.
The CE mark on the product denotes compliance with all applicable EU Directives. Note that the Notified Body
number does not apply to the RoHS (restriction of the use of certain hazardous substances in electrical and
electronic equipment) Directive.
Expected service life: Nebulizer handset, battery and mask adapter, 3 years from date of purchase
Symbol glossary
l
ON (power)
O
OFF (power)
Serial number
Follow instructions for use
Complies with RTCA/DO-160F
section 21, category M
IP22
Ingress Protection rating
1128271R02_InnoSpireGo_Euro2_Spreads_IFU_10B_FINAL.indd 13
10
Mouthpiece assembly, 1 year from date of first use
Masks, 1 year from date of first use
CAUTION
Alternating current
Separate collection
Atmospheric pressure
Manufacturer
Type BF applied parts
100
ENGLISH
Class II internally powered
device, double insulated
Direct current
Temperature limitation
Humidity
Date of manufacture
13
11/8/17 5:07 PM