FLAEM NebulFlaem 4.0 Bedienungsanleitung Seite 8

SYMBOLS ON DEVICE OR PACKAGING
Medical CE marking ref. regulation
2017/745 EU and subsequent updates
Class II device
Before use: Caution check instructions for
use
Function switch o
Function switch on
Phthalate- and bisphenol-free
Model number
Temperature limits
Atmospheric pressure limits
Batch Code
Protection rating of the envelope: IP21.
IP21
(Protected against solid bodies larger than 12
mm. Protected against access with a nger; Pro-
tected against vertically falling drops of water).
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: CONDOR F2000
Power supply:
Max. pressure:
Air ow to compressor:
Noise level (at 1 m):
Operation:
Dimension:
NEBULIZER TECHNICAL SPECIFICATIONS
Model: RF9-1
RF9 Nebuliser
Minimum drug capacity:
Maximum drug capacity:
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 identi er
230V~ 50Hz 210VA
3.5 ± 0.5 bar
14 l/min approx
55 dB (A) approx
Continued
20(L) x 29,5(D) x 10(H) cm
2 ml
8 ml
8
TECH
Model
Operat
APPLI
Type B
Weigh
ENVI