V2.1 UQ1399A P168A Quickstart for standard systems.doc Page 7 of 8
Plesio Pager Specification
Power:
1.3mm 9V DC
Weight:
144g
Material:
White ABS Anti-microbial
Dimensions (mm):
120 x 70 x 20 (HxWxD)
Batteries:
2x AA (HR6) Ni-MH Rechargeable 2500mAh
Battery Life:
80 hours (100 typical)
Charging time:
12 hours
The system complies with 93/42/EEC as a Class 1 Medical Device for use in a Home Heathcare
environment
The system complies with EN60601 for Class 2 Electrical Safety and does not need a protective earth
and Group 1 Class B for EMC in a Home Healthcare environment
The system has a Class 2 radio receiver compliant to EN300-220 operating at 434.075MHz wideband
Safety info
This symbol indicates there are warnings and precautions associated with
the use of this equipment. This instruction manual should be carefully read
and understood before using the equipment.
1.
Only the recommended power supply shall be used as it is certified to provide two
means of patient protection to EN60601-1
2.
Ensure the power cable is routed to avoid a trip hazard
3.
Regularly check the power supplies for damage and potential shock risks
4.
Clean and disinfect each item regularly in accordance with information on page 7
5.
Ensure, by testing, that the alarm is annunciated at the carer's location(s)
6.
Use only the power supply and batteries recommended
7.
Operate power supply and charge pager away from direct heat and uncovered.
8.
As with all medical electronic equipment there is potential for the equipment to
interfere with or be effected by interference from other electrical or electronic
devices. For this reason avoid placing the monitor, sensor or connecting cable in
close proximity to sensitive electronic devices or devices which produce strong
electromagnetic fields such as radio transmitters, mobile phones or power cables.
9.
Only use the monitor with accessories approved for use with this product and only
in accordance with instructions.
10.
If the equipment is modified in any way, appropriate inspection and testing must
be conducted to ensure continued safe use of the equipment.
11.
The carer must conduct a risk assessment to determine if the level of reliability
offered by the monitor is sufficient or if additional monitoring is needed. Contact
the manufacture for assistance with Risk Evaluation Tools.
