Starck Sefam S.Box Duo S, Руководство для пациента

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S.Box Duo S and S.Box Duo ST Technical characteristics  37
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CEI 60601-1-2:2014 + A1:2020: Medical electrical equipment – Part 1-2: General requirements for
basic safety and essential performance – Collateral Standard: Electromagnetic disturbances –
Requirements and tests.

IEC 60601-1-6:2010: Medical electrical equipment - Part 1-6: General requirements for basic safety
and essential performance - Collateral standard: Usability

ISO 80601-2-70:2015: Medical electrical equipment -- Part 2-70: Particular requirements for basic
safety and essential performance of sleep apnea breathing therapy equipment.

ISO 80601-2-74:2017: Respiratory tract humidifiers for medical use -- Particular requirements for
respiratory humidification systems.

ISO 80601-2-79:2018: Medical electrical equipment -- Part 2-79: Particular requirements for basic
safety and essential performance of ventilatory support equipment for ventilatory impairment.
End-of-life disposal of the device
In European Union this device has to be considered as an electrical and electronic piece of equipment
as defined in Directive 2012/19/EU, and must be collected and processed separately from household
waste for disposal as indicated by the symbol of the crossed out garbage bin (see "Definition of
symbols" page 8).
In other countries, this device must be processed following local regulation.
Unsuitable disposal of the device at the end of its life could harm the environment.
Contact your home care provider.