Philips AVENT SCF394/52 Manual página 34

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Idiomas disponibles

English
34
Symbol
Explanation
Indicates the relative humidity upper limits to which the device can be safely exposed: up to
18
90 %.
Indicates the storage and transportation temperature limits to which the medical device can
be safely exposed: ‑20 °C to 45 °C/‑4 °F to 113 °F.
Indicates the Forest Stewardship Council (FSC).
Indicates that the breast pump must be kept out of direct sunlight.
Indicates that the breast pump must be kept dry.
Indicates the operating pressure range: 700 to 1060 hPa.
Indicates that this device contains a rechargeable battery which must be disposed of properly.
See chapter 'Disposal' for more information.
Indicates that the adapter is certified by Intertek.
1 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
2 ISO 15223-1, Medical devices – Symbols to be used with medical device labels, labelling and information
to be supplied, Part 1: General requirements, Clause 5.4.4 Caution
3 This symbol is not contained in a standard that is recognized by the FDA
4 ISO/IEC 16022, Information technology - Automatic identification and data capture technologies - Data
Matrix barcode symbology specification
5 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
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 5.1.3 Date of manufacture
7 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
8 IEC 60601-1, Medical electrical equipment – Part 1: General Requirements for basic safety and essential
performance, Table D.1 Symbol 9 Class II equipment
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 5.1.6 Catalogue number
10 IEC 60601-1, Medical electrical equipment – Part 1: General Requirements for basic safety and essential
performance, Table D.1 Symbol 1 Direct current
11 IEC 60601-1, Medical electrical equipment – Part 1: General Requirements for basic safety and essential
performance, Table D.1 Symbol 4 Alternating current
12 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)
13 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)
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Este manual también es adecuado para:

Avent scf394/62Avent scf392/62