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SYMBOLS ON DEVICE OR PACKAGING
Medical CE marking ref. regula-
tion 2017/745 EU and subsequent
updates
Class II device
Before use: Caution check instruc-
tions for use
When you shut off the de-
Switch
vice, the switch will inter-
"ON"
rupt the compressor func-
tion only on one of the two
Switch
"OFF"
power phases
Phthalate- and bisphenol-free
Model number
Temperature limits
Atmospheric pressure limits
Batch Code
Quality mark
INFORMATION ON RESTRICTIONS OR INCOMPATIBILITIES WITH CER-
TAIN SUBSTANCES
• Interactions: The materials used in the device are biocompatible materials and comply with statutory
regulations, however possible allergic reactions cannot be completely excluded.
• Use the medicine as soon as possible once it has been opened and avoid leaving it in the nebuliser;
once therapy has ended, do not leave the medicine inside the nebuliser and proceed with hygienic
preparation.
COMPRESSOR UNIT SPECIFICATIONS
Model:
P0211EM F400
Power supply:
Max. pressure:
Air flow to compressor:
Noise level (at 1 m):
Operation:
Dimension:
Serial number of the device
Manufacturer
Type BF applied part
Alternating current
Attention
See instructions for use
Medical device
Moisture limits
Production date
Unique device identifier
Protection rating of the envelope: IP21.
(Protected against solid bodies larger than 12
IP21
mm. Protected against access with a finger;
Protected against vertically falling drops of
water).
230V~ 50Hz 130VA
1.8 ± 0.3 bar
9 l/min approx
54 dB (A) approx
Continued
13.5(L) x 15.5(W) x 11(H) cm
17
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