36
Technical characteristics
S.Box Duo S and S.Box Duo ST
Power supply
Power supply class II:
Input voltage:
100 – 240 VAC, 50 - 60 Hz
Power supply provided:
MDS-090BAS24 A (outlet depending on the
country)
Input current:
2 - 1 A
Output voltage:
24 V
WARNING:
Use only the plug-in power supply provided with the device
The power supply is not intended to be repaired. In case of a breakdown, please contact your home care
provider for a replacement.
The 24 V
DC
input is protected against voltage reversals.
Physical characteristics
Dimensions (L x W x H):
245 x 140 x 110 mm with side cover
245 x 185 x 110 mm with humidifier
Carrying bag dimensions (L x W x H):
305 x 245 x 180 mm
Carrying case dimensions (L x W x H):
350 x 310 x 190 mm
Weight (without power supply):
1.4 kg with side cover
1.7 kg with humidifier
Power supply weight:
0.5 kg
Operational volume (minimum volume of gas
in the humidifier chamber):
730 ml
Usable volume of water in humidifier chamber 350 ml
Maximum liquid level:
Indicated by
on humidifier chamber
CE marking
Date of CE marking of S.Box Duo S: 2021
Date of CE marking of S.Box Duo ST: 2021
Regulatory Requirements
Risks concerning this medical device are evaluated according to the ISO 14971:2019 standard,
specifically with regard to global residual risk.
Risks concerning this medical device are evaluated according to the ISO 14971 standard, specifically
with regard to global residual risk.
The S.Box Duo S or S.Box Duo ST complies with the following Directives and standards:
Directive 93/42/EEC of the European Parliament and of the Council concerning medical devices,
modified by the European Directive 2007/47/CE.
Directive 2014/53/EU of the European Parliament and of the Council on the harmonization of the
laws of the Member States relating to the making available on the market of radio equipment.
Directive 2011/65/EU of the European Parliament and of the Council on the restriction of the use of
certain hazardous substances in electrical and electronic equipment (RoHS).
Directive 2012/19/EU of the European Parliament and of the Council on waste electrical and
electronic equipment (WEEE).
Federal Aviation Administration RTCA/DO-160G section 21 category M.
CEI 60601-1:2005 + A1:2012: Medical electrical equipment. Part 1: General requirements for basic
safety and essential performance.
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