1 Safety
1.1 Instructions for safe operations
Check the main unit and all accessories periodically to make sure that there is no visible damage that
may affect patient's safety and monitoring performance about cables and transducers. It is
recommended that the device should be inspected once a week at least. When there is obvious
damage, stop using the device. In addition ,the overall check of monitor, including the safety check
such as the leakage current ,should be performed only by qualified personnel once every 12 months.
Necessary maintenance must be performed by qualified service engineers ONLY.
There are no user serviceable parts and users are not permitted to maintain it by
themselves.
The oximeter cannot be used together with devices not specified in User's Manual.
Only the accessory that appointed or recommendatory by manufacture can be used
with this device.
This product is calibrated before leaving factory.
1.2 Warning
Explosive hazard—DO NOT use the oximeter in environment with inflammable
gas such as some ignitable anesthetic agents.
Ensure that the environment in which the device is operated is not subject to any
sources of strong electromagnetic interference, such as radio transmitters, mobile
telephones, etc. Keep them far away High level electromagnetic radiation emitted
from such devices may greatly affect the monitor performance.
DO NOT use the oximeter while the testee measured by MRI and CT.
Be careful with the use of the lanyard cord. Improper use of the lanyard cord will cause device
damage not covered under the manufacturer's warranty. Swinging the device by the lanyard
cord will void the warranty. Please do not use lanyard cord if allergic to lanyard cord.
The person who is allergic to rubber cannot use this device.
The disposal of scrap instrument and its accessories and packing's (including
battery, plastic bags, foams and paper boxes) should follow the local laws and
regulations.
Please check the packing before use to make sure the device and accessories are
totally in accordance with the packing list, or else the device may have the
possibility of working abnormally.
Please choose the accessories and probe which are approved or manufactured by
the manufacturer, or else it may damage the device.
Please don't measure this device with functional tester for the device's related information.
When uploading, do keep the patient form touching the USB port. The computer used when
uploading must be in accordance with EN60950.We recommended to use Lenovo Qitian
M320,etc,in addition, when the data line connected to a computer, the medical electrical
systems should be in accordance with IEC60601-1-1.
CMS-50D Plus
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