HoMedics Salter Instructions And Guarantee - page 3
GB
3
CAUTION
• This device is intended for adult use only.
• This device is intended for non-invasive measuring and monitoring of arterial blood pressure. It is not intended for
use on extremities other than the arm or for functions other than obtaining a blood pressure measurement.
• Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood pressure. Do not
begin or end medical treatment, relay solely on a doctor for treatment advice.
• If you are taking medication,consult your physician to determine the most appropriate time to measure your blood
pressure. Never change a prescribed medication without consulting your physician.
• This unit is not suitable for continuous monitoring during medical emergencies or operations.
• If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the cuff not deflate
when pressures exceeds 40 kPa (300 mmHg), detach the cuff from the arm and press the any button to stop
inflation.
• To avoid measurement errors, carefully read this manual before using the product.
• The equipment is not AP/APG equipment and not suitable for use in the presence of a flammable anesthetic mixture
with air of with oxygen or nitrous oxide.
• The operator shall not touch output of AC adapter and the patient simultaneously.
• To avoid measurement errors, please avoid strong electromagnetic field radiated interference signal or electrical
fast transient/burst signals when using the AC adaptor.
• The user must check that the equipment functions safely and see that it is in proper working condition before being
used.
• Please note that Luer lock connectors are not used on the product and please DO NOT change any provided
connectors. Do not wind the air tube round the neck.
• Please use ACCESSORIES and detachable parts specified/ authorised by MANUFACTURER.
• Otherwise, it may cause damage to the unit or danger to the user/patients.
• Manufacturer will make available on request circuit diagrams, component parts list etc.
• After the cuff inflated long time, the patient’s arm and fingers will is insufficient, anaesthesia, destending pain and
ecchymosis.
• Please use the device under the environment which was provided in the user manual, otherwise, the performance
and lifetime of the device will been impacted and reduced.
• During use, the patient will 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 alergic reaction or
contact injury.
• At least two years of reliable service, without need for calibration.
• Please dispose of ACCESSORIES, detachable parts, and the EQUIPMENT according to the local guidelines.
• When the device is used to measure patients who have common arrhythmias such as atrial or ventricular
premature beats or artrial fibrillation, results may vary. Please consult your physician about the result.
• This device is contraindicated for any female subject who may be suspected of, or is pregnant. Besides provided
inaccurate readings, the affects of this device on the fetus are unknown.