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2
Components and Operation
2.1
Design
Page 20
A
rt.
no.
: 0-48-
0227
Rev.:
g
DEFIGARD/PHYSIOGARD Touch 7
2 Components and Opera-
tion
The
DEFIGARD
®
Touch 7
is a lightweight mains and battery powered defibrillator
featuring an ECG monitor, SpO2/SpCO/SpMet, etCO2,Temperature and NIBP
measurements. It is designed for clinical use. Defibrillation is possible in non-
synchronised or synchronised mode.
Moreover, the device can be switched to automated defibrillation (AED operation) by
pressing a single key
The
PHYSIOGARD
®
Touch 7
includes the same features as the
DEFIGARD
®
Touch
7
, but without the defibrillation function.
2.1 Design
Power supply
The
DEFIGARD
®
Touch 7
and
PHYSIOGARD
®
Touch 7
is powered by an integrated
rechargeable battery. The capacity of one battery is sufficient for:
DEFIGARD
®
Touch 7
• 100 shocks with maximum energy or
• >6 hours of monitoring
PHYSIOGARD
®
Touch 7
• >6 hours of monitoring
The battery is recharged by an external DC supply.
Defibrillator
The
DEFIGARD
®
Touch 7
is a defibrillator featuring biphasic pulsed defibrillation
impulse –
Multipulse Biowave
®
. The defibrillation is done using disposable
adhesive electrodes (pads), which also measure the ECG signal for the analysis.
Adhesive electrodes for children and adults are available. The device recognises the
connected electrodes and selects the defibrillation energy levels accordingly. In the
AED mode, the user will be given visual and audible instructions (display/
loudspeaker).
Monitoring
According to its configuration, the
DEFIGARD
®
Touch 7
and
PHYSIOGARD
®
Touch
7
monitoring function gives all important parameters – ECG, SpO2/SpCO/SpMet,
etCO2, RR, NIBP, IBP and Temperature. The parameters are indicated in figures and
as waveforms on the large 7” (800x480) LCD display.
Data storage
All intervention data – resting ECG data, lead II ECG, defibrillator ECG, SpO2 curves,
trends, events, patient data.
Data transmission
• Easy transmission of a 12-lead ECG, trends and screenshots by WLAN or GSM
during intervention
• GSM, WLAN, Ethernet (via USB adapter) Communication, for software and
configuration updates and post-intervention data (PDF or Sema format)
transmissions.
Biocompatibility
The parts of the product described in this user guide, including all accessories, that
come in contact with the patient during the intended use, fulfil the biocompatibility
requirements of the applicable standards. If you have questions in this matter, please
contact SCHILLER.