Spengler neotens NEO300 Gebrauchsanweisung Seite 38

5. People suffering from vascular constriction, liver disorders or diabetes, people with cardiac pacemakers or a weak pulse, and
women who are pregnant should consult their doctor before measuring their blood pressure themselves. Different values may
be obtained due to their condition.
6. People suffering from arrhythmias such as atrial or ventricular premature beats or atrial fibrillation only use this blood pressure
monitor in consultation with your doctor. In certain cases, oscillometric measurement method can produce incorrect readings.
7. The cuff should not be placed on the arm on the side of a mastectomy. In the case of a double mastectomy use the side of the
least dominant arm.
8. Pressurization of the cuff can temporarily cause loss of function of simultaneously used monitoring equipment on the same limb.
9. A compressed or kinked connection hose may cause continuous cuff pressure resulting in blood flow interference and potentially
harmful injury to the patient.
10. Check that operation of the unit does not result in prolonged impairment of the circulation of the patient.
11. Use only the approved arm cuff for this unit. Use of other arm cuffs may result in incorrect measurement results.
12. The system might produce incorrect readings if stored or used outside the manufacturer's specified temperature and humidity
ranges.
13. Only use the recommended Spengler Class II AC adaptor double-insulated complying with EN 60601-1 and EN 60601-1-2. An
unauthorized adapter may cause fire and electric shock.
14. Advising operator that the user manual must be consulted.
15. The time required for the device to warm from the minimum storage temperature (-25°C) between use until the device is ready
for use at Ambient Temperature 20°C: about 2 hours.
16. The time required for the device to cool from the maximum storage temperature (70°C) between use until the device is ready for
use at ambient temperature (20°C): about 2 hours.
17. The ME equipment shall not be used in operating rooms, nor under emergency circumstances, nor during patient transportation
or movement.
18. The ME equipment shall be usable in general-purpose offices such as professional healthcare facilities.
19. The ME equipment shall be usable at home for general-purpose exams.
20. During the intended use, the device shall not be connected to an external power source other than the provided PSU.
21. The device shall not be used or exposed to conditions outside of its specifications.
22. The product is not a toy, do not allow children under 12 to use it. Do not leave within reach of children. Do not use on children
under 12, risk of serious injury or thrombosis.
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