MDS4003 | MEDLINE 7
* When in use, please avoid compression or restriction of the connection tubing.
* The device cannot be used with HF surgical equipment at the same time.
* The accompanying document shall disclose that the sphygmomanometer was
clinically investigated according to the requirements of ISO 81060-2:2013.
* To verify the calibration of the automated sphygmomanometer, please contact
the manufacturer.
* This device is contraindicated for any female who may be suspected of, or is pregnant.
Besides providing inaccurate readings, the effects of this device on the fetus are
unknown.
* Too frequent and consecutive measurements could cause disturbances in blood
circulation and injuries.
* This unit is not suitable for continuous monitoring during medical emergencies or
operations; the user’s wrist and fingers may become anaesthetic, swollen
and even purple due to a lack of blood.
* When not in use, store the device in a dry room and protect it against extreme
moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on the
unit.
* This device may be used only for the purpose described in this booklet. The manufac-
turer cannot be held liable for damage caused by incorrect application.
* This device comprises sensitive components and must be treated with caution.
Observe the storage and operating conditions described in this booklet.
* The maximum temperature that the applied part can be achieved is 42.5˚С while the
environmental temperature is 40˚С.
* 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.
* Warning: Do not attempt to service the device while it is in use.
* The user is an intended operator.
* The user can measure data and change battery under 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 home use only. If you are
allergic to polyester, nylon or plastic, please don’t use this device.
* During use, the user 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 wrist or other
complaints, press the START/STOP button to release the air immediately from the cuff.
Loosen the cuff and remove it from your wrist.
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