Technical Specifications; Electromagnetic Compatibility; Device Disposal - FLAEM Latty P0117EM Mode D'emploi

TECHNICAL SPECIFICATIONS

Mod. P0117EM
Power supply:
Maximum vacuum in the pump in expression mode:
Noise (at 1 m):
Operation:
Operating conditions:
Temperature:
Air humidity:
Atmospheric pressure:
Storage conditions:
Temperature:
Air humidity:
Atmospheric pressure:
Safety approvals:
Dimensions:
Weight:
APPLIED PARTS
Type BF applied parts are:

ELECTROMAGNETIC COMPATIBILITY

This device was designed to meet the current requirements for electromagnetic compatibility (EN 60 601-1-2). Electro-
medical devices require particular care during installation and use relative to EMC requirements. Users are therefore
required to install and/or use these devices following the manufacturer's specifications. There is a risk of potential
electromagnetic interference with other devices, in particular with other test and treatment devices. RF mobile or
portable radio and telecommunications devices (mobile telephones or wireless connections) might interfere with the
operation of electro-medical devices. For additional information please go to www.flaem.it. The Medical Device may be
subject to electromagnetic interference if there are other devices used for specific diagnosis or treatments.
Flaem reserves the right to make technical and functional modifications to the product with no prior warning.

DEVICE DISPOSAL

In compliance with Directive 2012/19/EC, the symbol printed on the device shows that the device to be
disposed of is considered waste and must therefore be "collected separately". Consequently, the user must take
said waste (or have it taken) to the designated collection facilities arranged by the local authorities, or hand
it to the retailer when purchasing an equivalent new device. Separate waste collection and the subsequent
treatment, recycling and disposal procedures promote the production of devices made with recycled materials and
limit the negative effects on the environment and on health caused by any waste mismanagement. Illegal disposal of
the product by the user entails administrative penalties according to the transposition laws of directive 2012/19/EC of
the member state or country where the product is disposed of.
230V ~ 50Hz 140VA
-0.50 bar approx
< 60 dB (A) approx.
Continuous
min 5°C; max 40°C
min 10%; max 95%
min 69KPa; max 106KPa
min -25°C; max 70°C
min 10%; max 95%
min 69KPa; max 106KPa
26(W) x 12(D) x 23.5(H) cm
2.100 Kg
patient accessories (C2, C3, C4)
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