FLAEM Suction Pump Bedienungsanleitung Seite 10

UNIT TECHNICAL FEATURES
Mod. SUCTION PUMP
Voltage:
In conformity with EEC directive 93/42
Adjustable vacuum level:
Compressor air output:
Dimensions:
Weight:
Sound level (at 1 m):
Continuous use
Operating conditions:
Storage conditions:
Operating/storage atmospheric pressure: min. 690 hPa; max. 1060 hPa P
APPLIED PARTS
Type BF applied parts include:
SYMBOLS
Class II unit
Type BF unit
Attention: check the instructions for use
Switch "OFF"
When you shut off the device, the switch will interrupt the
compressor function only on one of the two power phases
Switch "ON"
Alternate current
Hazard: electrocution.
Consequence: Death.
Do not use device while taking a bath or shower
Disposable
Sterilisation by means of ethylene oxide
Latex Free
In compliance with European standard EN 10993-1 Biological evaluation
of medical devices and 93/42/EEC Medical Devices Directive
Serial number of device
Manufacturer
Keep dry
Disposal: In conformity with Directive 2012/19/EC, the symbol shown on the appliance to be disposed of indicates that this
is considered as waste and must therefore undergo "sorted waste collection". The user must therefore take (or have taken)
the above waste to a pre-sorted waste collection centre set up by the local authorities, or else give it back to the dealer when
purchasing a new appliance of the same type. Pre-sorted waste collection and the subsequent treatment, recovery and disposal operations
favour the production of appliances made of recycled materials and limit the negative effects of any incorrect waste management on the
environment and public health. The unlawful disposal of the product by the user could result in administrative fines as provided by the
laws transposing Directive 2012/19/EC of the European member state in which the product is disposed of.
Electromagnetic compatibility This device has been designed to satisfy requirements currently required for electromagnetic compatibility
(EN 60 601-1-2:2007). Electrical medical devices require special care. During installation and use with respect to EMC requirements,
it therefore required that they be installed and/or used according to the manufacturer's specification. Potential risk of electromagnetic
interference with other devices, in particular with other devices for analysis and treatment. Radio and mobile telecommunications
devices or portable RF (mobile phones or wireless connections) may interfere with the operation of electrical medical devices. For further
information visit www.flaemnuova.it. Flaem reserves the right to make technical and functional changes to the product without notice.
230V ~ 50Hz 140VA / 115V ~ 60Hz / 220V ~ 60Hz
from 0 to -0.4 bar approx.
11 l/min. approx.
22x17x17 cm
2.100 kg
60 dB (A) approx
Temperature: min. 10°C; max. 40°C
Air humidity: min. 10%; max. 95% RH
Temperature: min. -25°C; max. 70°C
Air humidity: min. 10%; max. 95% RH
patient accessories (C4)
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