20
WARNING
•
Do not apply the cuff over a wound, otherwise it can cause further injury.
•
Do not inflate the cuff on the same limb which other monitoring ME
EQUIPMENT is applied around simultaneously, because this could cause
temporary loss of function of those simultaneously-used monitoring
ME EQUIPMENT. Using it in case to result in prolonged impairment of the
circulation of the blood of the PATIENT.
•
Don’t kink the connection tube, otherwise, the cuff pressure may
continuously increase which can prevent blood flow and result in harmful
injury to the PATIENT.
•
The device has been evaluated clinically used manual cuff/stethoscope
auscultations the reference. Blood pressure measurements determined
with this device are equivalent to those obtained by a trained observer
using the cuff/stethoscope auscultatory method, within the limits prescribed
by the “American National Standard, Manual, electronic or automated
sphygmomanometers”.
•
The patient is an intended operator. The patient can measure under
normal circumstances and maintain the device and its accessories
according to the user manual.
•
The blood pressure monitor, and the cuff are suitable for use within the
patient environment. If you are allergic to dacron or plastic, please don’t
use this device.
•
Please keep the unit out of reach of infants, children or pets, since
inhalation or swallowing of small parts is dangerous or even fatal.
•
If Luer lock connectors are used in the construction of tubing, there is a
possibility that they might be inadvertently connected to intravascular fluid
systems, allowing air to be pumped into a blood vessel.
•
The device is not suitable for public use.
•
The device is not intended for PATIENT transport outside a healthcare
facility.
•
This device cannot be used with HF surgical equipment at the same time.
•
Be careful to strangulation due to cables and hoses, particularly due to
excessive length.
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