BMB MEDICAL CAREXIA FP, Руководство пользователя

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BMB MEDICAL – CAREXIA – 1VCRX092020 76
4.1.2 CONTRAINDICATIONS
There are no noteworthy contraindications for this device.
4.1.3 PRECAUTION ASSOCIATED WITH EQUIPMENT CARE AND MAINTENANCE
The device must not be altered in any way without the manufacturer’s prior consent: the
alteration could lead to unpredictable operation, potentially injuring the patient and
caregivers.
Torn upholstery no longer presents an effective antibacterial barrier and must hence be
replaced as soon as possible.
The device must be regularly inspected, at least once per year.
To maintain the device in good condition and to guarantee its safe and durable operation, the
prescribed maintenance must be performed. See the maintenance check-list that can be
downloaded from your customer area at https://www.bmb-medical.com or from your
distributor.
In the event of observed anomalies or damage that could jeopardize device operation and
safety, the equipment must be immediately withdrawn.
The device should only be used according to the instructions in this user manual.
The device must not be exposed to, or even less be in contact with, sources of heat, combustion
and flammable agents.
Work on electrical parts should only be performed by qualified and authorized staff.
* BMB MEDICAL will accept no liability in the event of incidents or accidents resulting from
improper use or alteration of the product by the buyer or user.