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D9U001SW0-0101_02
Staff:
►
Hospital staff (nurses, doctors) who studied at a high school specialised in healthcare, or at university (EU) and
who have completed training in operating the system.
Use:
►
The system is designed for application environments 1, 2, 3 and 5, pursuant to Czech Technical Standard EN
60601-2-52.
3.3 Contraindications
The SafetyMonitor system is contraindicated for the following use:
►
Use for any bed other than Eleganza 5 with scales or Eleganza 4 with scales.
►
The SafetyMonitor system is not designed to monitor patients weighing less than 35 kg.
NOTE:
The system is designed for hospital or care facilities. The electrical installation must conform to local
standards.
3.4 Ambient Conditions
The SafetyMonitor system must be used and stored under the following conditions:
Ambient temperature
10 °C – 35 °C
Relative humidity
30% to 75%
Atmospheric pressure
795 – 1060 hPa
Environmental conditions
2011/65/EU (RoHS), 2002/96/EC (WEEE)
Electromagnetic compatibility
CISPR 11:2015
Ambient sound pressure level
54 dBA (minimum volume of Bed Exit Alarm signal is 60
dBA)
The system is not suitable for:
►
Environments containing fl ammable gases (except oxygen).
3.5 Storage Conditions
1 week
-20 °C – 45 °C
1 month
-20°C – 35°C
3.6 Supported Beds
The SafetyMonitor system can be used only with the following beds:
►
Eleganza 5
►
Eleganza 4
NOTE:
The SafetyMonitor system can be used only in EMR beds with an integration module.
NOTE:
This list is current as of the publication date of these Instructions. Please contact Customer Services
for an up-to-date list.
3.7 Compatible mattress
The mattress dimensions must be as specifi ed in the Instructions for Use for Eleganza 5 bed or for Eleganza 4 bed.
Avoid improper adjustment of the mattress by compressing it.
