Certifier FA English 1980436 PDF
Certifier FA English 1980436 PDF
Certifier FA English 1980436 PDF
TEST SYSTEM
OPERATORS MANUAL
OPERATORS MANUAL
Caution
TSI flowmeters are not medical devices under FDA 510(k) and in no
situation should be used for human measurements.
The foregoing is IN LIEU OF all other warranties and is subject to the LIMITATIONS stated
herein. NO OTHER EXPRESS OR IMPLIED WARRANTY OF FITNESS FOR
PARTICULAR PURPOSE OR MERCHANTABILITY IS MADE. WITH RESPECT TO
SELLERS BREACH OF THE IMPLIED WARRANTY AGAINST INFRINGEMENT, SAID
WARRANTY IS LIMITED TO CLAIMS OF DIRECT INFRINGEMENT AND EXCLUDES
CLAIMS OF CONTRIBUTORY OR INDUCED INFRINGEMENTS. BUYERS EXCLUSIVE
REMEDY SHALL BE THE RETURN OF THE PURCHASE PRICE DISCOUNTED FOR
REASONABLE WEAR AND TEAR OR AT SELLERS OPTION REPLACEMENT OF
THE GOODS WITH NON-INFRINGING GOODS.
i
DEFECTIVE SOFTWARE OR IF UNABLE TO DO SO, WILL REFUND THE PURCHASE
PRICE OF THE SOFTWARE. IN NO EVENT SHALL SELLER BE LIABLE FOR LOST
PROFITS OR ANY SPECIAL, CONSEQUENTIAL OR INCIDENTAL DAMAGES. SELLER
SHALL NOT BE RESPONSIBLE FOR INSTALLATION, DISMANTLING OR
REINSTALLATION COSTS OR CHARGES. No Action, regardless of form, may be
brought against Seller more than 12 months after a cause of action has accrued. The
goods returned under warranty to Seller's factory shall be at Buyer's risk of loss, and will be
returned, if at all, at Seller's risk of loss.
Buyer and all users are deemed to have accepted this LIMITATION OF WARRANTY AND
LIABILITY, which contains the complete and exclusive limited warranty of Seller. This
LIMITATION OF WARRANTY AND LIABILITY may not be amended, modified or its terms
waived, except by writing signed by an Officer of Seller.
Service Policy
Knowing that inoperative or defective instruments are as detrimental to TSI as they are
to our customers, our service policy is designed to give prompt attention to any
problems. If any malfunction is discovered, please contact your nearest sales office or
representative, or call TSI's Customer Service department at (800) 874-2811 / (1) 651
490-2811 (USA and International) or TSI Instruments in UK at: +44 (0) 1494 4 59200.
ii
Contents
1 INTRODUCTION .......................................................................................... 1
1.1 Parts List ......................................................................................................... 3
1.2 Glossary ........................................................................................................... 6
2 SETUP ............................................................................................................ 7
3 OPERATION............................................................................................... 13
3.1 Power Up ......................................................................................................13
3.2 Keypad Functions .....................................................................................14
3.3 Displaying Test Measurements ..........................................................14
3.4 Measurements ............................................................................................15
3.4.1 Flow Rate ......................................................................................15
3.4.2 Peak Flow Rate ...........................................................................16
3.4.3 Volume ...........................................................................................16
3.4.4 Minute Volume ...........................................................................16
3.4.5 Stacked Volume .........................................................................16
3.4.6 Oxygen Concentration ............................................................17
3.4.7 Low Pressure ..............................................................................17
3.4.8 Peak Pressure .............................................................................18
3.4.9 Peep Pressure .............................................................................18
3.4.10 Breath Rate ..................................................................................18
3.4.11 I:E Ratio .........................................................................................18
3.4.12 I Time..............................................................................................19
3.4.13 Absolute Pressure .....................................................................19
3.4.14 Oxygen Concentration ............................................................19
3.5 Required Pre-test Calibrations ...........................................................19
3.5.1 Low-Pressure Transducer Zero Calibration .................19
3.5.2 Oxygen Sensor Calibration....................................................20
3.6 Breathing Cycles and Trigger Levels ................................................20
3.6.1 Inhalation and Exhalation Timing .....................................21
3.6.2 Flow Trigger Levels..................................................................21
3.7 Display Information .................................................................................22
4 TROUBLESHOOTING .............................................................................. 25
5 MAINTENANCE ......................................................................................... 29
5.1 Replacing the Batteries (as required)..............................................29
5.2 Replacing the Oxygen Sensor (yearly) ............................................29
iii
5.3 Cleaning (as required) ............................................................................29
5.4 Factory Calibration (yearly).................................................................30
5.5 Return Procedure .....................................................................................30
6 SPECIFICATIONS ...................................................................................... 31
6.1 Physical..........................................................................................................31
6.2 Environmental............................................................................................31
6.3 Power .............................................................................................................31
6.4 Test Measurements ..................................................................................31
6.5 Calibration Requirements .....................................................................33
6.6 Compliance and Approvals ...................................................................33
List of Figures
Figure 1. The Certifier FA Test System ......................................................... 2
Figure 2. Certifier FA Test System Parts ...................................................... 3
Figure 3. Connecting the Controller Module to a Flow Module ........... 7
Figure 4. Connecting the Bacteria Filters to the Flow Modules ........... 8
Figure 5. Attaching Pressure Tubing to the High Flow Module ........... 9
Figure 6. Attaching the Oxygen Sensor to the High Flow
Module ...................................................................................................10
Figure 7. Installing a Flow Module into the Test Circuit .......................11
Figure 8. Certifier FA Test System Installed in an Oxygen
Concentrator Circuit ........................................................................12
Figure 9. Controller Module Keypad ..............................................................14
List of Tables
Table 1. Certifier FA Test System Parts List ............................................... 4
Table 2. Keypad Functions and Operation...................................................14
Table 3. Screen Displays ......................................................................................22
Table 4. Troubleshooting the Certifier FA Test System ......................25
Table 5. Cleaning Recommendations .............................................................29
iv
1 Introduction
The Certifier Flow Analyzer (FA) Test System allows you to test
respiratory care or other devices. This portable tester makes it simple to
test flows, volumes, pressures, oxygen concentration, and breath timing.
The Certifier FA Test System is designed for institutional, home care,
field service, and laboratory settings.
Certifier FA Test System components include:
Controller module:
The keypad and display allow you to select test measurements and
units for display. The controller module connects to a high or Low
Flow module.
High Flow module:
Measures air or 100% oxygen (O2) over a range of flows from 0 to
300 standard liters per minute (SLPM).
Low Flow module:
Measures air, 100% O2, or 100% nitrous oxide (N2O) over a range of
flows from 0.01 to 15 SLPM with greater accuracy than the High
Flow module at low flow rates.
Oxygen sensor:
Used with the High Flow module, allows the High Flow module to
measure O2 concentration and other measurements for any mixture
of air and O2.
You can connect or disconnect the flow modules and oxygen sensor at
any time during normal operation without interrupting tester
operation. Four AA batteries power the test system. The test system
conserves power by automatically turning off if none of the keys are
pressed for 15 minutes. See Section 3.1 to disable this feature.
1
Controller
module
Low Flow
module
Oxygen
sensor
High Flow
module
WARNING
To avoid the risk of explosion, do not use in the presence of
flammable anesthetic gases.
Only qualified and trained service technicians are authorized to
service the Certifier FA Test System. Use only factory-approved
parts and procedures to service the device.
CAUTION
To avoid inaccurate test readings, do not obstruct tubing or inlet or
exhaust ports, and always use dry gas.
To avoid damage to the Certifier FA Test System components,
always use bacteria filters upstream of the flow modules, and
always cap flow module ports when not in use.
TSI flowmeters are not medical devices under FDA 510(k) and in no
situation should be used for human measurements.
2 1: Introduction
1.1 Parts List
Carefully unpack the test system components from the shipping
container. Check the individual parts against the packing list and notify
TSI immediately if anything is missing or damaged. Table 1 summarizes
the Certifier FA Test System components and part numbers shown in
Figure 2.
1: Introduction 3
Table 1. Certifier FA Test System Parts List
Item Part
Description Qty
no. no.
4 1: Introduction
Table 1. Certifier FA Test System Parts List (cont)
Item Part
Description Qty
no. no.
Low Flow standard kit (part no. 4075)
1 Controller module 4078 1
13 Low Flow module 4074 1
14 Bacteria filter, barbed fittings, for use with 1040045 1
Low Flow module (single use)
4 Soft carrying case (holds Certifier FA Test 1319289 1
System and accessories)
9 Mounting bracket (includes mounting 1040044 1
bracket, screws, and Velcro strap)
10 Pocket driver (used to remove/install the 3012034 1
controller module battery cover)
11 AA batteries (not shown) NA 4
12 Certifier FA Test System Operators Manual 1980436 1
(not shown)
High Flow module kit (optional) (part no. 4076)
2 High Flow module 4071 1
3 Bacteria filter, 22-mm x 22-mm 1602341 1
male/female, for use with High Flow module
(single use)
5 Adapter, 15-mm ID x 22-mm OD 1102093 1
6 Airway pressure fitting with screen 1611330 1
7 Adapter, 22-mm x 6-mm (for interfacing 1102091 2
High Flow module to Low Flow filter, for use
with oxygen concentrator)
8 Pressure tubing, 1/8-in. ID x 1/4-in. OD x 3002053 1
48-in. length, silicone
9 Mounting bracket (includes mounting 1040044 1
bracket, screws, and Velcro strap)
1: Introduction 5
Table 1. Certifier FA Test System Parts List (cont)
Item Part
Description Qty
no. no.
1.2 Glossary
These labels, terms, and symbols appear on the Certifier FA Test
System:
Refer to manual: see Certifier FA Test System Operators
Manual for important information.
CE marking of European Conformity for the Low Voltage
Directive (LVD) and the Directive for Electromagnetic
Compatibility (EMCD).
6 1: Introduction
2 Setup
Follow these steps to set up the Certifier FA Test System:
CAUTION
To avoid damage to the Certifier FA Test System components, always
use bacteria filters upstream of the flow modules, and always cap flow
module ports when not in use.
1. Connect the controller module to a flow module (Figure 3).
To remove the cable, pull its locking connector (not the cable) from
the controller module.
Controller
module
Flow
module
7
2. Attach the bacteria filter to the flow module (Figure 4).
Install the bacteria filter to the flow module inlet or upstream of all
Certifier FA Test System components. Make sure the filter is in the
correct orientation by aligning the filters flow arrow with the
direction of the flow, ensuring that the filters inlet indicator
(labeled INLET, I, or other) faces upstream of the flow module,
or that the outlet indicator (label Patent side, Outlet or other)
faces towards the flow module.
Controller
module
Low Flow
filter
8 2: Setup
3. High Flow module only: install pressure tubing (Figure 5).
Attach one end of the pressure tubing to the low-pressure port on
the flow module, and the other to the pressure port in the circuit.
Pressure
tubing
2: Setup 9
4. High Flow module only: install the oxygen sensor (optional,
Figure 6).
Plug the oxygen sensor cable into the High Flow module and oxygen
sensor. Turn the cable collar to secure the cable to the oxygen
sensor. Use the threaded tee to install the oxygen sensor into the
circuit. The oxygen sensor can only connect to the High Flow
module.
Oxygen sensor
cable
Oxygen
sensor
Threaded tee
10 2: Setup
5. Install the flow module into the test circuit (Figure 7, Figure 8).
Align the flow direction of the flow module and filter with the
direction of flow through the circuit.
Ventilator
2: Setup 11
Oxygen
Concentrator
12 2: Setup
3 Operation
3.1 Power Up
Pull the protective caps from the flow module ports before powering up.
Do not apply pressure to the flow module at power up (this ensures
accurate low-pressure transducer zero calibration).
Press the I/O (on/off) key on the controller module to power up the
Certifier FA Test System (the controller module powers all of the
attached Certifier FA Test System components). At power up, the
controller module shows information in this sequence:
1. All LCD segments light (about two seconds).
NOTE: If battery voltage is below the minimum operating level, the
battery symbol lights and the controller module will turn off.
2. Firmware revision shown (about two seconds).
3. Controller module verifies connection and correct operation of the
flow module and oxygen sensor (if installed). If the oxygen sensor
is installed, the controller module will display a symbol.
4. Default measurements displayed:
High Flow module: flow (top line), low pressure (bottom line).
Low Flow module: flow (top line), respiratory rate (bottom line).
CAUTION
To ensure accurate measurements, wait about one minute for the
Certifier FA Test System to warm up. If environmental conditions
have changed significantly, more time may be necessary.
To avoid damage to the Certifier FA Test System components,
always use bacteria filters upstream of the flow modules, and
always cap flow module ports when not in use.
If liquid has penetrated any of its components, do not use, and
return to the factory for calibration.
13
3.2 Keypad Functions
Table 2 summarizes the primary functions of the Certifier FA Test
System keypad (Figure 9).
ON/OFF Backlight
key on/off key
14 3: Operation
You can change the display selections and connect or disconnect the
flow module or oxygen sensor at any time during normal operation.
If you disconnect the flow module, the controller module display is
blank.
If you disconnect the oxygen sensor, the sensor symbol and any
oxygen-related measurements are not shown on the display.
Normal operation and display resume about one second after
reconnection.
NOTE: The Certifier FA Test System automatically updates
measurements that are recalculated at every breath. The Certifier FA
Test System uses a threshold flow to determine the beginning and end
of each breath. The threshold flow calculated from the last three
breaths, is updated at each breath, and then is applied to the following
breath. Breath measurement displays begin after two full breaths.
CAUTION
To avoid damage to the Certifier FA Test System components, always
use bacteria filters upstream of the flow modules, and always cap flow
module ports when not in use.
3.4 Measurements
Measurements on Top Line of Display
The following parameters are displayed on the top line of the display.
The Top Line Select key is used to scroll through parameters by
momentarily pressing and then releasing the key.
3:Operation 15
3.4.2 Peak Flow Rate
Maximum flow rate during the inhalation cycle of a breath can be
displayed on the top line of the control module display. Units of
standard liters per minute, indicated by PEAK SLPM, and actual liters
per minute, indicated by LPM, can be selected using the DISPLAY
UNITS key. See Section 3.7, Display Information, for definitions of
these units of measure. For the High Flow module air, O2, and air/O2
mixtures can be selected using the GAS SELECT key. For the Low Flow
module air, O2, and N2O can be selected using the GAS SELECT key.
NOTE: A valid flow cycle must occur for this value to be displayed. See
Section 3.6, Breathing Cycles and Trigger Levels, for details.
3.4.3 Volume
Volume that occurs during the inhalation cycle of a breath can be
displayed on the top line of the control module display. Units of actual
liters, indicated by ATP L; standard liters, indicated by STP L; or
liters at body temperature and pressure saturated, indicated by BTPS
L can be selected using the DISPLAY UNITS key. See Section 3.7,
Display Information, for definitions of these units of measure. For the
High Flow module air, O2, and air/O2 mixture can be selected using the
GAS SELECT key. For the Low Flow module air, O2, and N2O can be
selected using the GAS SELECT key.
NOTE: A valid flow cycle must occur for this value to be displayed. See
Section 3.6, Breathing Cycles and Trigger Levels, for details.
16 3: Operation
actual liters, indicated by ATP S L; standard liters, indicated by STP S
L; or liters at body temperature and pressure saturated, indicated by
BTPS S L can be selected using the DISPLAY UNITS key. See Section
3.7, Display Information, for definitions of these units of measure. For
the High Flow module air, O2, and air/O2 mixture can be selected using
the GAS SELECT key. For the Low Flow module air, O2, and N2O can be
selected using the GAS SELECT key.
NOTE: A valid flow cycle must occur for this value to be displayed. See
Section 3.6, Breathing Cycles and Trigger Levels, for details.
NOTE: The symbol will appear on the display when the oxygen
cable is attached.
3:Operation 17
3.4.8 Peak Pressure
Peak gauge pressure from the low-pressure port of the High Flow
module during the inhalation cycle can be displayed on the bottom line
of the control module display. Select units of PEAK cmH2O or PEAK
mmHg by pressing and holding the DISPLAY UNITS key for at least
three seconds.
NOTE: A valid flow cycle must occur for this value to be displayed. See
Section 3.6, Breathing Cycles and Trigger Levels, for details.
For best results check the zero on the low pressure transducer before
measurements. See Section 3.5.1 for instructions on zeroing the
pressure transducer.
18 3: Operation
3.4.12 I Time
The inhalation time (I TIME) can be displayed on the bottom line of the
control module display.
NOTE: A valid flow cycle must occur for this value to be displayed. See
Section 3.6, Breathing Cycles and Trigger Levels, for details.
NOTE: The inhalation time is defined as the time of positive inhalation
flow and does not include the breath hold time. If the vents pause
inhalation time includes a pause time, the Certifier FAs I time will not
match the vents I time.
NOTE: The symbol will appear on the display when the oxygen
cable is attached.
3:Operation 19
2. Momentarily press the Bottom line select key until low pressure
(see Section 3.4.7) is shown on the display.
3. Press and hold the Bottom line select key for 2 to 3 seconds. The
display shows ZERO to indicate that the zero calibration is in
progress.
4. When ZERO is no longer displayed, the low-pressure transducer
zero calibration is complete.
NOTE: The barometric pressure transducer does not require a zero
calibration.
20 3: Operation
3.6.1 Inhalation and Exhalation Timing
At the beginning of the inhalation cycle the flow rate must be above the
trigger flow rate for at least 0.25 milliseconds. If this time is less than
0.25 milliseconds, the Certifier FA considers this part of the exhalation
cycle. When a valid inhalation cycle is ending and the flow rate goes
below the trigger level, the flow rate must remain below the trigger level
for at least 0.25 milliseconds, otherwise, this period is included in the
inhalation cycle.
If testing of ventilator pressure modes is needed, a test lung must be
used to ensure that a long enough flow delivery time is generated. If
there is not enough volume in the breathing circuit, the pressure can be
generated in less than 0.25 milliseconds.
3:Operation 21
NOTE: The default value of 20% auto trigger is restored once the
controller module is turned off.
Display Meaning
--- An out-of-range measurement.
Oxygen sensor symbol: indicates presence of oxygen
sensor. Flashes to indicate that sensor must be
calibrated or replaced.
Low battery voltage symbol: indicates that batteries
should be replaced.
22 3: Operation
Table 3. Screen Displays (cont.)
Display Meaning
CAL 100% O2 Oxygen sensor calibration in progress (during
exposure to 100% O2).
CAL 21% O2 Oxygen sensor calibration in progress (during
exposure to room air).
cmH2O Centimeters of water: a unit of pressure.
I TIME Inspiratory time (in seconds). Can be displayed on the
bottom line (either High Flow or Low Flow module
attached).
I:E RATIO Ratio of inspiratory time to expiratory time, can be
displayed on the bottom line (when High Flow or Low
Flow module is attached).
L Liter: a unit of volume.
LPM Liters per minute: a unit of flow. The Certifier FA
Test System calculates the LPM value by applying the
actual gas temperature and pressure to the SLPM
measurement.
MINUTE VOL Minute volume: an estimate of exhaled volume for the
next 60 seconds, based on the current breath. Can be
displayed on the bottom line (when High Flow or Low
Flow module is attached).
mmHg Millimeters of mercury: a unit of pressure.
N 2O 100% nitrous oxide supply gas, selected using the GAS
SELECT key (if Low Flow module is attached).
O2 100% oxygen supply gas, selected using the GAS
SELECT key (when High Flow or Low Flow module is
attached).
PEAK Peak flow or pressure. Peak flow can be displayed on
top line (when High Flow or Low Flow module is
attached). Peak pressure can be displayed on bottom
line (if High Flow module is attached).
PEEP Positive end expiratory pressure: the minimum
pressure measured in the circuit throughout the
breath cycle. Can be displayed on the bottom line (if
High Flow module attached).
REV Software revision level, displayed at power up.
3:Operation 23
Table 3. Screen Displays (cont.)
Display Meaning
S Stacked volume: a cumulative volume measurement
for consecutive breaths. The top line shows the
cumulative volume and the bottom line shows the
number of consecutive breaths.
SEC Seconds, a unit of time for I TIME measurements.
SLPM Standard liters per minute: a unit of flow. The
Certifier FA Test System measures flows in SLPM.
Standard conditions are defined as 21.1 C (70 F) at
101.3 kPa (14.7 psia).
STP Standard temperature and pressure: a condition of
volume measurement. The Certifier FA Test System
measures volumes at STP. Standard conditions are
defined as 21.1 C (70 F) at 101.3 kPa (14.7 psia).
VOL Volume: the exhaled volume for the most recent
breath. Can be displayed on the top line (either High
Flow or Low Flow module attached).
ZERO Low-pressure transducer zero calibration in progress.
24 3: Operation
4 Troubleshooting
Table 4 lists the symptoms, possible causes, and recommended
corrective actions for problems you may encounter with the
Certifier FA Test System. If the symptom is not listed, or if none of the
recommended corrective actions solves the problem, please contact TSI
Customer Support at (800) 874-2811 or 651-490-2811.
25
Table 4. Troubleshooting the Certifier FA Test System (cont.)
26 4: Troubleshooting
Table 4. Troubleshooting the Certifier FA Test System (cont.)
4:Troubleshooting 27
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28 4: Troubleshooting
5 Maintenance
Component Cleaning
Controller module Clean exterior as required with a clean
Flow modules cloth and isopropyl alcohol, hydrogen
peroxide (3%), or ammonia (15%).
Carrying cases
Oxygen sensor
Oxygen sensor cables
Tee Steam autoclave after contact with any
Adapters non-sterile breathing circuit components,
and discard if any damage is visible.
Single use filters (high Discard after contact with any non-sterile
and Low Flow breathing circuit components or if
modules) damage is visible.
29
5.4 Factory Calibration (yearly)
Certifier FA Test System flow modules are designed for one year of
normal use following each factory calibration.
If the test system has been dropped or liquid has penetrated any of its
components, do not use, and return to the factory for calibration.
Recalibrated flow modules come with a certificate of calibration and a
summary of performance before and after the calibration. A factory
calibration consists of pressure transducer calibration over the full
range of pressures and calibration over the full range of flows. All
calibration datum are stored in the flow modules, so the controller
module does not require calibration. Therefore, it is not necessary to
return the controller module for factory calibration.
Follow the steps in Section 5.5 to return Certifier FA Test System flow
modules for factory calibration.
30 5: Maintenance
6 Specifications
NOTE: Specifications are subject to change without notice.
6.1 Physical
Dimensions Controller module: 13.2 cm x 7 cm x 3.3 cm (5.2 in. x 2.8 in. x 1.3 in.).
High Flow module: 18 cm x 6.6 cm x 4 cm (7.1 in. x 2.6 in. x 1.6 in.).
Low Flow module: 12.7 cm x 5.1 cm x 2.8 cm (5.0 in. x 2.0 in. x 1.1 in.).
Flow High Flow module:
connectors
flow inlet: 22-mm female ISO taper.
flow outlet: 22-mm male ISO taper.
Low Flow module:
flow inlet: 0.25-in. barb.
flow outlet: 0.25-in. barb.
Weight Approximately 1.36 kg (3 lb) for the standard kits.
6.2 Environmental
Temperature Operating: 5 to 40 C (41 to 104 F). 15 to 80% relative humidity from 5
to 31 C decreasing linearly to 15 to 50% relative humidity at 40 C.
Storage: -40 to 70 C (-40 to 158 F) at 10 to 95% relative humidity.
Atmospheric Operating: 57.1 to 106 kPa (8.28 to 15.37 psia).
Pressure Storage: 50 to 106 kPa (7.25 to 15.37 psia).
Conditions Indoor Use
Operating Altitude up to 4000 m (13,000 ft)
Pollution degree I or II
6.3 Power
Battery life 15 to 20 hours.
Battery type Four commercially available AA batteries.
31
Measurement High Flow Module Low Flow Module
Pressure drop Maximum between inlet and outlet Maximum between inlet and
ports at 101.3 kPa (14.7 psia) outlet ports at 101.3 kPa (14.7
including filter: 0.50 cmH2O at psia) including filter: 4 cmH2O at
20 SLPM, 1.50 cmH2O at 50 SLPM, 2 SLPM, 16 cmH2O at 5 SLPM, 45
5.0 cmH2O at 100 SLPM, 30.0 cmH2O at 10 SLPM, 85 cmH2O at
cmH2O at 300 SLPM. 15 SLPM.
Volume
Range 0.01 to 10.0 L STP. 0 to 9.999 L STP.
Accuracy Air and oxygen: 2% of reading Air and oxygen: 2% of reading
plus 0.020 L STP or 0.010 L STP, whichever is
Air/oxygen mixtures: 4% of greater.
reading plus 0.020 L STP. Nitrous oxide: 4% of reading
or 0.010 L STP, whichever is
greater.
Minute Volume
Range 0 to 99.00 L STP. 0 to 9.999 L STP.
Accuracy 7% of reading. 7% of reading.
Stacked Volume
Range 0 to 99.00 L STP. 0 to 9.999 L STP.
Accuracy Air and oxygen: 2% of reading Air and oxygen: 2% of reading
plus 0.020 L STP or 0.010 L STP, whichever is
Air/oxygen mixtures: 4% of greater.
reading plus 0.020 L STP. Nitrous oxide: 4% of reading
or 0.010 L STP, whichever is
greater.
Inspiratory Time
Range 0.25 to 60.00 seconds. 0.25 to 60.00 seconds.
Accuracy 0.01 seconds. 0.01 seconds.
I:E Ratio
Range 1:100.0 to 100.0:1. 1:15.0 to 15.0:1.
Accuracy 5% of reading. 5% of reading.
Respiratory Rate
Range 0.5 to 120.0 breaths per minute. 0.5 to 120.0 breaths per minute.
Accuracy 5% of reading. 5% of reading.
Low Pressure
Range -25.0 to 150.0 cmH2O. Not applicable.
(-18.4 to 110 mmHg)
Accuracy 0.75% of reading or Not applicable.
0.20 cmH2O (0.15 mmHg),
whichever is greater.
32 6: Specifications
Measurement High Flow Module Low Flow Module
Peak & PEEP Low Pressure
Range 0 to 150.0 cmH2O. Not applicable.
(0 to 110 mmHg)
Accuracy 0.75% of reading or 0.20 Not applicable.
cmH2O (0.15 mmHg), whichever is
greater.
Barometric Pressure
Range 375 to 1500 mmHg. 375 to 1500 mmHg.
Accuracy 8 mmHg. 8 mmHg.
Oxygen Concentration
Range 0 to 100.0% O2. Not applicable.
Accuracy 2% O2 at daily calibration Not applicable.
conditions.
NOTES
1. Standard conditions are defined as 21.1 C (70 F) and 101.3 kPa (14.7 psia).
2. Flow and volume accuracy is applicable in SLPM or STP mode only.
3. The temperature of the gas and the ambient air must be within 10 C ( 18 F) of each
other and the gas must be less than 30% relative humidity at 21. 1 C (70 F).
4. Flow and volume accuracy de-rating: 0.075% of reading per 1 C (1.8 F) away from
21.1 C (70 F); 0.015% of reading per 1.03 kPa (0.15 psia) above 101.3 kPa (14.7
psia); 0.022% of reading per 1.03 kPa (0.15 psia) below 101.3 kPa (14.7 psia);
0.07% of reading per 1% relative humidity above 30% relative humidity.
6: Specifications 33
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