Medela Freestyle Flex Mode D'emploi page 47

Symbols on the motor unit (cont.)
Indicates that this device contains Bluetooth wireless technology. (Trademarks of Bluetooth
Special Interest Group (SIG))
The Regulatory Compliance Mark indicates the compliance with Australian EMC and radio
transmission requirements.*
The CE mark indicates conformity with the European low voltage and electromagnetic
compatibility directive.*
Indicates direct current.
Symbols on the power adaptor
Indicates alternating current.
Indicates direct current.
Indicates the polarity of the USB power output.
Indicates that the device is a Class II electrical appliance (double insulated).
Indicates that the device is for indoor use only.
Indicates the efficiency level for external power supplies.
The UL LISTED mark indicates that the product is manufactured in compliance with UL safety
requirements for USA and Canada (USA: UL60950-1, CAN: CSA C22.2 NO. 60950-1).
Indicates the compliance with the requirements of the Federal Communications Commission.
The NOM (Norma Oficial Mexicana) mark indicates that the product is found to be in
compliance with the applicable Mexican requirements.
References
6 ISO 15223-1, Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied, Part 1: General requirements,
Clause 5.1.1 Manufacturer
7 ISO 15223-1, Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied, Part 1: General requirements,
Clause 5.1.3 Manufacturing Date / ISO 7000-2497, Graphical symbols for use on equipment, Date of manufacture
8 ISO 15223-1, Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied, Part 1: General requirements,
Clause 5.1.6 Article number / ISO 7000- 2493, Graphical symbols for use on equipment, Catalogue number
9 ISO 15223-1, Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied, Part 1: General requirements,
Clause 5.1.7 Serial number / ISO 7000-2498, Graphical symbols for use on equipment, Serial number
10 IEC 60601-1, Medical electrical equipment – Part 1: General Requirements for basic safety and essential performance, Table D.3 Symbol 2 IP Code IEC
60529:1989+A1:1999+A2:2013, Degrees of protection provided by enclosures (IP Code)
11 IEC 60601-1, Medical electrical equipment – Part 1: General Requirements for basic safety and essential performance, Table D.1 Symbol 20 Type BF
applied parts
12 EN 50419, Marking of Electrical and Electronic Equipment in accordance with Article 11(2) of Directive 2002/96/EC (WEEE).
13 TÜV (Technical Inspection Association) mark indicates that the product is manufactured in compliance with UL safety requirements for USA and Canada
(USA: UL60950-1, CAN: CSA C22.2 NO. 60950-1).
14 IEC 60601-1, Medical electrical equipment – Part 1: General requirements for basic safety and essential performance, Table D.2 Symbol 10 Refer to
instruction manual/booklet
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