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• Warning: No servicing/maintenance while the ME
equipment is in use.
• The patient is an intended operator.
• The patient can measure data and change batteriesunder
normal circumstances and maintain the device and its
accessories according to the user manual.
• To avoid measurement errors, please avoid the condition
of strong electromagnetic field radiated interference signal
or electrical fast transient/burst signal.
• The blood pressure monitor and the cuff are suitable for
use within the patient environment. If you are allergic to
polyester, nylon or plastic, please don't use this device.
• During use, the patient will be in contact with the cuff.
The materials of the cuff have been tested and found to
comply with requirements of ISO 10993-5:2009 and ISO
10993-10:2010. It will not cause any potential sensization
or irritation reaction.
• If you experience discomfort during a measurement,
such as pain in the arm or other complaints, press the
START/STOP button to release the air immediately from the
cuff. Loosen the cuff and remove it from your arm.
• If the cuff pressure reaches 40 kPa (300 mmHg), the
unit will automatically deflate. Should the cuff not deflate
when pressures reaches 40 kPa (300 mmHg), detach the
cuff from the arm and press the START/STOP button to
stop inflation.
• Before use, make sure the device functions safely and is
in proper working condition. Check the device, do not use
the device if it is damaged in any way. The continuous use
of a damaged unit may cause injury, improper results, or
serious danger.
• Do not wash the cuff in a washing machine or
dishwasher!
• The service life of the cuff may vary by the frequency
of washing, skin condition, and storage state. The typical
service life is 10000 times.
• It is recommended that the performance should be
checked every 2 years and after maintenance and repair,
by retesting at least the requirements in limits of the error
of the cuff pressure indication and air leakage (testing at
least at 50mmHg and 200mmHg).
• Please dispose of ACCESSORIES, detachable parts, and
the ME EQUIPMENT according to the local guidelines.
• Manufacturer will make available on request circuit
diagrams, component part lists, descriptions, calibration
instructions,etc., to assist to service personnel in parts
repair.
• The operator shall not touch output of batteries and the
patient simultaneously.
• Cleaning: Dust environment may affect the performance
of the unit. Please use the soft cloth to clean the whole
unit before and after use. Don’t use any abrasive or volatile
cleaners.
• The device doesn’t need to be calibrated within two years
of reliable service.
• If you have any problems with this device, such as
setting up, maintaining or using, please contact the
SERVICE PERSONNEL of Salter. Don’t open or repair the
device by yourself in the event of malfunctions. The device
must only be serviced, repaired and opened by individuals
at authorized sales/service centers.
• Please report to Salter if any unexpected operation or
events occur.
• Keep the unit out of reach of infants, young children or
pets to avoid inhalation or swallowing of small parts. It is
dangerous or even fatal.
• Be careful to strangulation due to cables and hoses,
particularly due to excessive length.
• At least 30 min required for ME equipment to warm from
the minimum storage temperature between uses until it
is ready for intended use. At least 30 min required for ME
equipment to cool from the maximum storage temperature
between uses until it is ready for intended use.
• This equipment needs to be installed and put into
service in accordance with the information provided in the
ACCOMPANYING DOCUMENTS;
• Wireless communications equipment such as wireless
home network devices, mobile phones, cordless telephones
and their base stations, walkie-talkies can affect this
equipment and should be kept at least a distance d away
from the equipment. The distance d is caculated by the
MANUFACTURER from the 80 MHz to 5.8 GHz column of
Table 4 and Table 9 of IEC 60601-1-2:2014, as appropriate.
• Please use ACCESSORIES and detachable parts specified/
authorised by MANUFACTURER. Otherwise, it may cause
damage to the unit or danger to the user/patients.
• There is no luer lock connectors used in the construction
of tubing, there is no possibility that they might be
inadvertently connected to intravascular fluid systems,
allowing air to be pumped into a blood vessel.
• Please use the device under the environment which was
provided in the user manual. Otherwise, the performance
and lifetime of the device will be impacted and reduced.
