Weinmann MEDUMAT Standard2 Instructions For Use Manual page 14

2 Safety
Caution
14 EN MEDUMAT Standard
Fault or treatment failure due to incompatibility of the device
with consumables, accessories or other medical devices!
Defective and unauthorized accessories can result in malfunctions,
increased electromagnetic interference emissions and reduced
electromagnetic immunity of the device, incorrect output values
and reduced ventilation performance. This can result in serious or
life-threatening injury to the patient.
⇒ Only connect approved accessories.
Risk of injury through electric shock if the device is touched!
Accessories which are connected to the device may cause an
electrical potential in the device. This may lead to an electric shock
on contact with the device and result in injury to the user.
⇒ Only use accessories from WEINMANN Emergency.
Risk of injury as a result of pressure variations during use in
combination with devices from the WEINMANN Emergency
MODUL range!
If the device is used together with devices from the
WEINMANN Emergency MODUL range, the flow used by devices
from the WEINMANN Emergency MODUL series may cause
pressure variations in the device. This can injure the patient.
⇒ Only use the device and devices from the
WEINMANN Emergency MODUL range in combinations
approved by WEINMANN Emergency.
Prevent interference between the devices!
Electrical devices which are operated directly next to or on top of
each other can cause mutual interference to functionality.
Portable high-frequency communication devices in the direct
vicinity of the device can also influence the functioning of the
device.
⇒ Do not stack the device with other electrical devices.
⇒ Do not operate the device directly next to other electrical
devices. Exception: Other WEINMANN Emergency devices
which have been tested and shown to guarantee interference-
free operation with the adjacent device. A list of other devices
is available on request.
⇒ If stacking or operation in the immediate vicinity cannot be
avoided: Closely monitor the functioning of all affected
medical electrical devices and do not use if functions are
disrupted.
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