Riester RVS-100 Manual Del Usuario página 46

1.3 Configurations
The monitor consists of main unit, NIBP cuff, SpO2 sensor, Tempe-
rature sensor (optional) and printer (optional). It can connect to the
optional RVS-200 Wall Diagnostic Station through DC output. The
connection details are provided the corresponding manual for the
RVS-200 Wall Diagnostic Station.
1.4 Main Unit
1.4.1 Front View

Significant levels of dysfunctional
hemoglobins (such as carboxyhemoglobin or
methemoglobin);

Incorrect sensor application or use;

Placement of a sensor on an extremity with a
blood pressure cuff, arterial catheter or
intravascular line;

Low perfusion;

Electrosurgical units.
• Do not use the SpO sensor on the same limb
2
being used for NIBP measurement. This may
result in inaccurate SpO reading due to
2
blocked blood flow during cuff inflation.
• Do not measure SpO on a finger painted with

Significant levels of 2 dysfunctional
nail polish. This may result in unreliable
hemoglobins (such as carboxyhemoglobin or
measurements.
methemoglobin);

Do not measure NIBP on patients with

Incorrect sensor application or use;
sickle-cell disease or any condition in which

Placement of a sensor on an extremity with a
skin damage has occurred or is expected.
blood pressure cuff, arterial catheter or

Use clinical judgment to decide whether to
intravascular line;
perform frequent Auto BP measurements on

Low perfusion; 1) Physiological alarm visual indicator LED's. When a physiological
patients with severe blood clotting disorders

Electrosurgical units.
alarm occurs, this lamp will light up as defined below:
because of the risk of hematoma in the limb
• Do not use the SpO sensor on the same limb
2
fitted with the cuff.
being used for NIBP measurement. This may

Use clinical judgment to decide whether to
result in inaccurate SpO reading due to
2
perform Auto BP measurement on patients
blocked blood flow during cuff inflation.
with thrombasthemia.
• Do not measure SpO on a finger painted with
 2
Do not use the NIBP cuff on a limb with an
nail polish. This may result in unreliable
2) LCD Touchscreen
intravenous infusion or arterial catheter in
measurements.
place. This could cause tissue damage around
 3) SpO2 connector
Do not measure NIBP on patients with
the catheter when the infusion is slowed or
sickle-cell disease or any condition in which
4) NIBP connector
blocked during cuff inflation.
skin damage has occurred or is expected.

NIBP Measurement Limitations: Accurate NIBP
 5) USB connector x 2
Use clinical judgment to decide whether to
measurements cannot be taken when the heart
perform frequent Auto BP measurements on
6) Power button
rate is extremely low (less than 40 bpm) or
patients with severe blood clotting disorders
extremely high (greater than 240 bpm) or if the
because of the risk of hematoma in the limb
patient is on a heart-lung machine. Accurate
fitted with the cuff.
measurement also cannot be taken when the

Use clinical judgment to decide whether to
following conditions exist:
perform Auto BP measurement on patients

excessive and continuous patient movement
with thrombasthemia.
7) Battery charging indicator LED
such as shivering or convulsions;

Do not use the NIBP cuff on a limb with an

difficulty detecting a regular arterial pressure
intravenous infusion or arterial catheter in
pulse;
place. This could cause tissue damage around

cardiac arrhythmias;
the catheter when the infusion is slowed or

rapid blood pressure changes;
blocked during cuff inflation.

severe shock or hypothermia that reduces

NIBP Measurement Limitations: Accurate NIBP
blood flow to the peripheries; 8) Power indicator LED. Status of the LED is specified as follows:
measurements cannot be taken when the heart

an edematous extremity.
rate is extremely low (less than 40 bpm) or

MRI may lead to vessel damage;
extremely high (greater than 240 bpm) or if the
patient is on a heart-lung machine. Accurate
measurement also cannot be taken when the
following conditions exist:
1.3 Configurations

excessive and continuous patient movement
The monitor consists of main unit, NIBP cuff, SpO
2
9) Well for Temp Probe Cover box (20pcs)
such as shivering or convulsions;
Temperature sensor (optional) and printer (optional). It can

difficulty detecting a regular arterial pressure
connect to the optional RVS-200 Wall Diagnostic Station
10) Covidien Filac 3000 temp probe
pulse;
through DC output The connection details are provided the

corresponding manual for the RVS-200 Wall Diagnostic cardiac arrhythmias;

rapid blood pressure changes;
Station.
1.4.2 Side View

severe shock or hypothermia that reduces
blood flow to the peripheries; Right side:
1.4 Main Unit

an edematous extremity.
1.4.1 Front View

MRI may lead to vessel damage;
3 Configurations
e monitor consists of main unit, NIBP cuff, SpO sensor,
2
mperature sensor (optional) and printer (optional). It can
nnect to the optional RVS-200 Wall Diagnostic Station
ough DC output The connection details are provided the
rresponding manual for the RVS-200 Wall Diagnostic
ation.
4 Main Unit
4.1 Front View
46
BP measurement on patients with thrombasthemia.
• Do not use the NIBP cuff on a limb with an intravenous
infusion or arterial catheter in place. This could cause
tissue damage around the catheter when the infusion is
slowed or blocked during cuff inflation.
• NIBP Measurement Limitations:
measurements cannot be taken when the heart rate
is extremely low (less than 40 bpm) or extremely high
(greater than 240 bpm) or if the patient is on a heart-
lung machine. Accurate measurement also cannot be
taken when the following conditions exist:
◊ excessive and continuous patient movement such as
shivering or convulsions;
◊ difficulty detecting a regular arterial pressure pulse;
◊ cardiac arrhythmias;
◊ rapid blood pressure changes;
◊ severe shock or hypothermia that reduces blood flow
to the peripheries;
◊ an edematous extremity.
• MRI may lead to vessel damage;
Fig.1-1 Fig.1-1
1) Physiological alarm visual indicator LED's. When a
physiological alarm occurs, this lamp will light up as defined Caution: Devices connected to this monitor must
below:
meet the requirements of the applicable IEC
• High level alarm: the lamp quickly flashes red.
standards (e.g. IEC 60950 safety standards for
• Medium level alarm: the lamp slowly flashes yellow.
information technology equipment and IEC 60601-1
• High level alarm: the lamp quickly flashes red.
• Low level alarm: the lamp lights yellow without flashing.
safety standards for medical electrical equipment).
2) LCD Touchscreen
• Medium level alarm: the lamp slowly flashes yellow.
The system
3) SpO connector
2
• Low level alarm: the lamp lights yellow without flashing.
4) NIBP connector
requirements of the IEC 60601-1 medical electrical
5) USB connector x 2
systems standard. Any personnel who connect
6) Power button
devices to this monitor's signal input/output port is
Press this button to turn on the monitor after AC power is
•
responsible for providing evidence that the safety
connected or the battery is installed.
Fig.1-1
certification of the devices has been performed in
• Press and hold for 3 seconds to turn the monitor off.
1) Physiological alarm visual indicator LED's. When a
7) Battery charging indicator LED accordance to the IEC 60601-1. If you have any
physiological alarm occurs, this lamp will light up as defined
On: When the battery is being charged.
below: • questions, please contact Riester. If it is not evident
Off: When the battery is fully charged or there is no battery in
•
• High level alarm: the lamp quickly flashes red.
from the
• Press this button to turn on the monitor after AC power is
monitor.
• Medium level alarm: the lamp slowly flashes yellow.
particular device combination is hazardous--for
8) Power indicator LED. Status of the LED is specified as
connected or the battery is installed.
• Low level alarm: the lamp lights yellow without flashing.
example,
follows:
2) LCD Touchscreen
• Press and hold for 3 seconds to turn the monitor off.
currents—please consult the manufacturers or an
Green: When the AC mains connected.
•
3) SpO connector
2
Orange: When the AC mains not connected and monitor is expert in the field to ensure the necessary safety of
•
4) NIBP connector
powered by battery.
5) USB connector x 2 patients and proper function of all connected devices.
• On: When the battery is being charged.
Off: When the AC mains not connected.
6) Power button •
• Off: When the battery is fully charged or there is no battery 9) Well for Temp Probe Cover box (20pcs)
Press this button to turn on the monitor after AC power is
•
10) Covidien Filac 3000 temp probe
connected or the battery is installed.
in monitor.
• Press and hold for 3 seconds to turn the monitor off.
Left side:
1.4.2 Side View
7) Battery charging indicator LED
Right side:
On: When the battery is being charged.
•
• Green: When the AC mains connected.
Off: When the battery is fully charged or there is no battery in
•
• Orange: When the AC mains not connected and monitor is Left side:
monitor.
8) Power indicator LED. Status of the LED is specified as
powered by battery.
follows:
• Off: When the AC mains not connected.
Green: When the AC mains connected.
•
sensor,
Orange: When the AC mains not connected and monitor is
•
powered by battery.
Off: When the AC mains not connected.
•
9) Well for Temp Probe Cover box (20pcs)
10) Covidien Filac 3000 temp probe
1.4.2 Side View
Right side:
Fig.1-2
1) Grounding terminal
2) Nurse call connector
3) AC power connector (input)
4) DC power connector (output)
5) USB socket x 2
6) Ethernet LAN Network connector
1.5 Equipment Symbols
Symbol
1.5 Equipment Symbols
2
Fig.1-2
Fig.1-2
1) Grounding terminal
2) Nurse call connector
3) AC power connector (input)
4) DC power connector (output)
5) USB socket x 2
6) Ethernet LAN Network connector
2
1) Grounding terminal
2) Nurse call connector
3) AC power connector (input)
4) DC power connector (output)
5) USB socket x 2
Accurate NIBP
6) Ethernet LAN Network connector
Left side:
1) Integrated Thermal Printer
1.4.3 Rear View
Caution: Devices connected to this monitor must
meet the requirements of the applicable IEC
standards (e.g. IEC 60950 safety standards for
configuration must meet the
information technology equipment and IEC 60601-1
safety standards for medical electrical equipment).
The system configuration must meet
requirements of the IEC 60601-1 medical electrical
systems standard. Any personnel who connect
devices to this monitor's signal input/output port is
responsible for providing evidence that the safety
certification of the devices has been performed in
equipment specifications whether a
accordance to the IEC 60601-1. If you have any
questions, please contact Riester. If it is not evident
due to summation of leakage
from the equipment specifications whether
particular device combination is hazardous--for
example, due to summation of
currents—please consult the manufacturers or an
expert in the field to ensure the necessary safety of
patients and proper function of all connected devices.
1.4.4 Bottom View
Symbol Note
Type CF applied part,
defibrillation protected
Symbol Symbol Note
The unit displaying this
Type CF applied part,
symbol contains an F-Type
defibrillation protected
isolated (floating) applied
The unit displaying this
part providing a high degree
symbol contains an F-Type
of protection against shock,
isolated (floating) applied
and is defibrillator-proof.
part providing a high degree
of protection against shock,
Refer to instruction
and is defibrillator-proof.
manual/booklet.
Refer to instruction
manual/booklet.
Non-ionizing radiation
Caution: Devices connected to this monitor must meet Caution: Devices connected to this monitor must
meet the requirements of the applicable IEC
the requirements of the applicable IEC standards (e.g.
standards (e.g. IEC 60950 safety standards for
IEC 60950 safety standards for information technology
information technology equipment and IEC 60601-1
equipment and IEC 60601-1 safety standards for me-
safety standards for medical electrical equipment).
dical electrical equipment). The system configuration The system configuration must
requirements of the IEC 60601-1 medical electrical
must meet the requirements of the IEC 60601-1 medical
systems standard. Any personnel who connect
electrical systems standard. Any personnel who connect
devices to this monitor's signal input/output port is
devices to this monitor's signal input/output port is re-
responsible for providing evidence that the safety
certification of the devices has been performed in
sponsible for providing evidence that the safety certifi-
accordance to the IEC 60601-1. If you have any
cation of the devices has been performed in accordance
questions, please contact Riester. If it is not evident
to the IEC 60601-1. If you have any questions, please
from the equipment specifications
contact Riester. If it is not evident from the equipment
particular device combination is hazardous--for
specifications whether a particular device combination example, due to summation
currents—please consult the manufacturers or an
is hazardous--for example, due to summation of leakage
expert in the field to ensure the necessary safety of
currents—please consult the manufacturers or an expert
patients and proper function of all connected devices.
in the field to ensure the necessary safety of patients and
proper function of all connected devices.
Left side:
Fig.1-3
1.5 Equipment Symbols
Fig.1-3
Symbol Symbol Note
1) Integrated Thermal Printer
Type CF applied part,
1.4.3 Rear View
defibrillation protected
Fig.1-3
The unit displaying this
1) Integrated Thermal Printer
symbol contains an F-Type
1.4.3 Rear View
isolated (floating) applied
part providing a high degree
of protection against shock,
the
and is defibrillator-proof.
Refer to instruction
manual/booklet.
Non-ionizing radiation
a
leakage
Dangerous voltage
Fig.1-4 Fig.1-4
1) Speaker
1) Speaker
1.4.4 Bottom View
Fig.1-4
Equipotential grounding
1) Speaker
1.4.4 Bottom View
USB socket
Network connector
1. Battery compartment
Caution: Clean the battery contacts regularly to ensure
1. Battery compartment
optimal electrical contact. Before cleaning, power down the
unit and disconnect it from A/C power. To clean the contacts,
Caution: Clean the battery contacts regularly to ensure
rub with a cotton swab dampened (not dripping wet) with
optimal electrical contact. Before cleaning, power down the
1. Battery compartment
isopropyl alcohol.
unit and disconnect it from A/C power. To clean the contacts,
Fig.1-5
rub with a cotton swab dampened (not dripping wet) with
isopropyl alcohol.
Caution: Clean the battery contacts regularly to ensure
optimal electrical contact. Before cleaning, power down
Symbol Symbol Note
the unit and disconnect it from A/C power. To clean the
contacts, rub with a cotton swab dampened (not dripping
Nurse call connector
Symbol Symbol Note
wet) with isopropyl alcohol.
Nurse call connector
Manufacture date
Manufacture date
Manufacturer
Catalog Number
Manufacturer
Batch or Lot Code Catalog Number
Serial number Batch or Lot Code
Serial number
Temperature limitation
1) Integrated Thermal Prin
1.4.3 Rear View
meet the
whether a
of leakage
1) Speaker
1.4.4 Bottom View
1. Battery compartment
Caution: Clean the battery contac
optimal electrical contact. Before c
unit and disconnect it from A/C po
rub with a cotton swab dampened
isopropyl alcohol.
Symbol
Nurse call co
Manufacture
Manufacture
Catalog Num
Batch or Lot
Serial numbe
Temperature
Humidity lim
Pressure lim
CE mark: Pro
Medical Dev
and is CE m
indicate conf
Fig.1-5
3
Fig.1-5
Fig
Fig.1-4
Symb