PhysioFlow Lab1, Руководство по обслуживанию

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M anatec B iomedical
21, Rue du stade, Petit Ebersviller
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57730 Folschviller
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France
Tél : +33 (0)3 72 82 50 00
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Fax : +33 (0)1 30 74 46 48
support@physioflow.com
Service Manual PhysioFlow Lab1 8 / 20
Version of Monday, 10 July 2017
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The device is used in accordance with the operating instructions.

Any modification of any electro medical PhysioFlow® device is forbidden.

PhysioFlow® Q-Link is designed to be reliable, effective and mechanically
robust. However it must be used with care.

PhysioFlow® devices have no particular protection against the penetration
of liquids. Do not allow liquids to get into the device.

Only patient cable provided by PhysioFlow® must be used. Any other use of
the patient cable is forbidden. Moreover, it can increase the
electromagnetic emissions and reduce the immunity of the device.

PhysioFlow® devices must not be sterilized.

FOR ACCURATE MEASUREMENTS, IT IS ESSENTIAL THAT THE OPERATOR
UNDERSTANDS THE DIFFERENCE BETWEEN ACCEPTABLE SIGNAL AND POOR
SIGNAL QUALITY. (cf.
PhysioFlow® Software manual, or third party monitor
manual).
Precautions
Some clinical circumstances may impair accuracy of measurements, such as:

Tachycardia with heart rate above 250 bpm

Untimely movement of neck
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Patients under 120cm (48 in.)
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Patients under 25 Kg (67 lbs.)

Presence of aortic balloon pumps
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Presence of ultrafiltration systems
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Presence of pacemakers with external leads

Open chest surgery

Use of electrical cutlery and electrosurgical devices

Morbidly obese patients, such as those weighting over 600 pounds.
Re-calibration can take place at the same time that the electrodes are replaced as a function of normal
nursing protocol. After 24 hours electrodes must be replaced.