Inhoudsopgave
Advertenties
Beschikbare talen
Beschikbare talen
12.2 Symbols
Safety instructions / warnings
Read and follow the instructions for use
Compliance with valid European regulations for
medical devices
0123
Manufacturer
Applied part BF type
The device is subject to the provisions of the
WEEE Directive 2002/96/EC
Protection class
Setting for the vacuum (suction level)
Vacuum
Medical device
MEDICAL — GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL
HAZARDS ONLY IN ACCORDANCE WITH ANSI/AAMI ES60601-1:2005 / ( R ) 2012 and A1:2012, C1:2009
( R ) 2012 and A2:2010 ( R ) 2012, CSA CAN/CSA-C22.2 NO. 60601-1:14, IEC 60601-1-6:2010/ AMD1:2013,
CSA CAN/CSA-C22.2 NO. 60601-1-6:11 AMD 1, ANSI/AAMI HA60601-1-11:2015, CSA CAN/CSA-C22.2 NO.
E358823
60601-1-11:15
13
Disposal
The device can be returned to the manufacturer or be dismantled and recycled in an environmentally responsible manner by
a recycling company specialising in electric devices. There are no special or increased risk factors. Waste must be disposed of
in compliance with local regulations.
14
Electromagnetic compatibility
The Ardo Alyssa breastpump meets all the relevant requirements for the applicable standards relating to interference emis-
sions and immunity for operation in medical and domestic environments.
More information about electromagnetic tests is given in the section 'Emission and Immunity Tests' (page 78).
Alternating current
Direct current
Temperature
Air pressure
Relative humidity
Store protected from sunlight
Keep the packaging away from moisture
Setting for the cycles (suction frequency)
Cycles
Device corresponds to the requirements
(Part 15) of the Federal Communications
Commission (FCC)
en
11
Advertenties
Inhoudsopgave
