en GB – 38
DreamStar Intro, Info, Auto patient manual
Transportation and storage conditions
Pressure range:
500 hPa to 1060 hPa
Temperature:
-20°C to +60°C (-4 °F to +140 °F)
Relative humidity:
Up to 95% without condensation
Device electrical characteristics
Universal internal electrical power with the detachable electrical power cord (which varies by country).
Input voltage (auto-ranging):
100 - 240 VAC (-15%, +10%), at 50 or 60Hz
Maximum power consumption:
100VA at maximum setting.*
Current consumed at 20cmH
2
O with a 4mm leak:
130 mA eff. at 230 VAC
DC power supply (13 V)
Voltage range allowed: 13V (-15%, +25%).
*Power consumption is based on the type of model. The DreamStar™ Auto™ Evolve with heated humidification
enabled is the highest-consumption device.
Physical characteristics
Dimensions (D x W x H):
200 x 230 x 120 mm (7.8 x 9.0 x 4.7 in) approximately
with water chamber
Carrying case Dimensions (D x W x H):
260 x 350 x 150 mm (10.2 x 13.7 x 5.9 in)
approximately
Weight:
1.5 kg (3.3 lbs) approximately with water chamber
1.4 kg (3.1 lbs) approximately with cover
Operational volume (minimal gas volume in water
chamber):
811 ml
Useful volume of water chamber:
300 ml
Maximum liquid fill level:
Indicated on water chamber
CE marking
DreamStar™ Intro, DreamStar™ Intro Evolve : 2011
DreamStar™ Info, DreamStar™ Info Evolve : 2011
DreamStar™ Auto, DreamStar™ Auto Evolve : 2011.
Standards compliance
Risks pertaining to this medical equipment were assessed in accordance with the ISO 14971:2007 standard,
specifically with reference to global residual risk.
The DreamStar™ product range device complies with the following standards.
•
CEI 60601-1:2005 + AC1:2006 + AC2:2007 + Amd1:2012: Medical electrical equipment. Part 1: General
requirements for basic safety and essential performance.
•
CEI 60 601-1-2:2007: Medical electrical equipment. Part 1: General requirements for safety. Collateral
standard: Electromagnetic compatibility – Requirements and tests.
•
EN ISO 17510-1:2009: Sleep Apnea Breathing Therapy Devices.
•
EN ISO 8185:2009: Respiratory tract humidifiers for medical use -- Particular requirements for
respiratory humidification systems.
•
Directive 93/42/EC of the Council concerning medical devices.
•
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).
Содержание DreamStar Auto
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