WM 68401 04/2021
MEDUCORE Standard
2
EN 17
2 Safety
Disrupted and failed therapy due to incorrect use of
disposables!
Reusing and reprocessing disposables might induce unpredictable
reactions as a result of aging, embrittlement, wear, thermal stress,
and chemical action. This may put the functionality and safety of
the device at risk, and cause the patient and user serious or life-
threatening injury.
Do not reuse disposables.
Do not subject disposables to hygienic reprocessing.
Risk of injury from using third-party accessories!
Accessories which have not been approved by
WEINMANN Emergency may result in explosions, electric shocks,
incorrect monitoring, impaired functions and a negative impact on
interference immunity and interference emission or lead to
material damage and injure the patient.
Only use accessories which have been approved by
WEINMANN Emergency (see “17.2 Accessories and other
parts”, page 360).
Delay in treatment due to overly loud audio output!
When the defibrillator is used in conjunction with devices with
audio output (e.g. alarm tones, voice prompts), overly loud audio
output from one device may drown out audio output from the
other device and thus delay treatment.
When using multiple devices with audio output at the same
time, set the volume on the devices to the same level.
Risk of injury and treatment delay due to imperceptible alarm
signals!
Alarm signals which are quieter than the ambient noise level
prevent alarm situations from being detected. This may result in
delayed treatment and thus in injury to the patient.
Always set device volume to be louder than ambient noise
level.
Do not stack devices.
Therapy at risk due to inadequate patient monitoring!
If the patient and the device are not observed and monitored
during therapy, delayed response by medical personnel to alarms
and faults may result in severe or life-threatening injury to the
patient and incorrect therapy.
Continuously observe and monitor the patient and device
during therapy.
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