THIS MANUAL MUST BE READ CAREFULLY PRIOR TO THE OPERATION OF THIS DEVICE.
THIS DEVICE WILL PERFORM AS DESIGNED ONLY IF USED IN ACCORDANCE WITH
THE MANUFACTURER’S INSTRUCTIONS. IMPROPER USE MAY CAUSE THE DEVICE TO
FAIL TO PERFORM AS DESIGNED AND MAY CAUSE INJURY TO THE PATIENT AND/OR
HEALTHCARE PROFESSIONAL.
The warranties made by Ohio Medical Corporation® with respect to these products are voided if the
products are not installed, used and serviced in accordance with the instructions in this manual.
Please protect yourself and your patients by following them. We encourage our customers to
write or call regarding this equipment prior to use or for any additional information relative to use
or repairs.
This product is not intended as a life-sustaining or life-supporting device.
FEDERAL (USA) LAW RESTRICTS THIS DEVICE TO SELL BY OR ON THE ORDER OF A
PHYSICIAN
Ohio Medical Corporation® | 1111 Lakeside Drive | Gurnee, IL 60031 USA
This product is sold by Ohio MedicalTM under the warranties set forth in the following paragraphs. Such
warranties are extended only with respect to the purchase of this product directly from Ohio Medical or Ohio
Medical’s Authorized Dealers as new merchandise and are extended to the rst Buyer thereof, other than
for purpose of resale.
For a period of twelve (12) months from the date of original delivery to Buyer, to Buyer’s order, or to an
Ohio Medical Authorized Dealer, this product, other than its expendable parts, is warranted to be free
from functional defects in materials and workmanship and to conform to the description of the product
contained in the service manual and accompanying labels and/or inserts, provided that the same is properly
operated under conditions of normal use, that regular periodic maintenance and service is performed and
that replacements and repairs are made in accordance with the instructions provided. This same warranty is
made for a period of sixty (60) days with respect to the expendable parts. The foregoing warranties shall not
apply if the product has been repaired other than by Ohio Medical or in accordance with written instructions
provided by Ohio Medical, or altered by anyone other than Ohio Medical, or if the product has been subject
to abuse, misuse, negligence, or accident.
Ohio Medical’s sole and exclusive obligation and Buyer’s sole and exclusive remedy under the above
warranties is limited to repairing or replacing, free of charge, at Ohio Medical’s option, a product, which is
telephonically reported to the nearest Ohio Medical Regional Service Ofce and which, if so advised by Ohio
Medical, is thereafter returned with a statement of the observed deciency, not later than seven (7) days
after the expiration date of the applicable warranty,to the designated Ohio Medical Service Ofce during
normal business hours, transportation charges prepaid, and which, upon Ohio Medical’s examination, is
found not to conform with the above warranties. Ohio Medical shall not be otherwise liable for any damages
including, but not limited to incidental damages, consequential damages, or special damages.
There are no express or implied warranties which extend beyond the warranties herein above set forth.
Ohio Medical makes no warranty of merchantability or tness for a particular purpose with respect to the
product or parts thereof.
P/N 474618 [Rev.2] 02/2016
MiniOX® 1 Oxygen Analyzer General WARNINGS and CAUTIONS
General WARNINGS and CAUTIONS
WARNING
1. The MiniOX® 1 Oxygen Analyzer will perform to
specications only if it is used and serviced in
accordance with the manufacturer’s instructions.
This instrument is to be used only by qualied,
trained personnel who have carefully read
the operating manual and labels and who
have observed the information set forth. If this
instrument does not perform as described in this
manual, the instrument must not be used until
the condition is rectied.
®
2. The MiniOX
1 Oxygen Analyzer must be
calibrated prior to each use. A two point
calibration check must be performed weekly. See Section 4, Operation. If the instrument cannot be
calibrated, the sensor must be replaced. If the
instrument still is unable to be calibrated, the
instrument must be serviced.
3. The oxygen sensor has a minimal response to
certain gases other than oxygen. Be aware of
these gases and their interference levels. See
Section 3, Performance Specications.
4. The oxygen sensor is affected by changes in
barometric pressure. See Section 4, Effects of Pressure, for the effects of pressure.
5. The sensor is a sealed unit containing a
potassium hydroxide electrolyte. If the sensor
should develop a leak, dispose of it immediately,
as the sensor contains caustic material. It must
be disposed of in accordance with all applicable
federal, state, and local regulations. Should
contact occur with skin or clothing, rinse area
immediately with large quantities of water. In
case of eye contact, immediately ush eyes with
water for at least 15 minutes, holding eyes open.
Call a physician.
6. Ensure a tight t exists between the sensor and
the tee adapter. Ohio Medical tee adapters are
engineered to t securely with Ohio Medical
sensors. However, the sensor retaining strap
must be used to prevent accidental separation
of sensor and tee adapter.
®
7. Never operate the MiniOX
1 Oxygen Analyzer
if it is suspected that water or other liquids have
entered into the case. If this occurs, immediately
turn the unit OFF and contact your nearest Ohio
Medical Service Center for additional information.
8. Use of devices generating or emitting electro
®
magnetic radiation near the MiniOX
1 Oxygen
Analyzer may interfere with the proper operation
of the product, causing it to fail to perform as
designed. Particularly, the electromagnetic
radiation from the interfering device may cause
the product to display incorrect/erratic values or
to stop operating. Special attention should be
paid to the patient if this occurs.
®
9. Never use the MiniOX
1 Oxygen Analyzer in
combustible atmosphere, such as occurs with
ammable anesthetics. Such use could result in
ignition of atmosphere.
10. Never allow an excess length of cable near the
patient’s head or neck, as such could result in
strangulation. Secure excess cable to the bed
rail or other suitable object.
FAILURE TO COMPLY WITH THESE WARNINGS
CAN RESULT IN SERIOUS INJURY OR DEATH
OF THE PATIENT.
CAUTION
1. Remove internal battery if unit is to be nonoperational for extended periods of time.
2. Observe polarity when inserting a new battery.
Incorrect connection may cause damage to the
instrument.
®
3. The MiniOX
1 Oxygen Analyzer must never be
immersed in any cleaning solution, autoclaved,
or exposed to temperatures greater than 70oC.
4. Use only Ohio Medical Corporation replacement
parts and accessories listed in Section 3, Accessories of this manual. Analyzers can
only be used with Ohio Medical Corporation
sensors. Failure to do so may seriously impair
the instrument’s performance.
5. Improper mounting of the sensor in a breathing
circuit may result in inaccurate readings. The
sensor MUST be mounted with the deector
pointing downward to prevent moisture
collection on the sensor membrane (see Figure 4-1 in Section 4, Operation). Install the sensor
upstream from the humidier to minimize its
exposure to moisture.
®
6. Never use a MiniOX
1 Oxygen Analyzer with
a cable that appears worn, cracked, or has
damaged insulation
FAILURE TO COMPLY WITH THESE CAUTIONS
CAN RESULT IN INSTRUMENT DAMAGE.
WC-1
P/N 474618 [Rev.2] 02/2016
MiniOX® 1 Oxygen Analyzer General WARNINGS and CAUTIONS
Denition of WARNINGS and CAUTIONS
WARNING
CAUTION
NOTE:
Statement citing a potential safety hazard and
possible injury to yourself or others.
Statement citing a possibility of damage to the
instrument or other property.
1 Home Care Kit Installation ............................................................. A-1
P/N 474618 [Rev.2] 02/2016
TOC-2
MiniOX
®
1 Oxygen Analyzer Section 1, Introduction
Section 1
Introduction
The MiniOX® 1 Oxygen Analyzer is designed to
provide continuous analyzing or spot checking of
oxygen for:
• ventilators
• incubators
• emergency transports
• oxygen tents
• concentrators
• various other respiratory therapy uses
WARNING
This instrument is not equipped with an
alarm, and is therefore not for use in a lifesupport system. Failure to comply with this
warning can jeopardize patient well-being.
The MiniOX® 1 Oxygen Analyzer (Figure 1-1):
• Operates by a single push of a button.
• Calibrates with the turn of a dial.
• Features an easy-to-read digital display.
For sensor connection, a tee adapter is provided
with each instrument.
The galvanic oxygen sensor measures oxygen
concentrations from 0 to 100%. The sensor is
maintenance-free and will operate for one year, in
normal medical use.
WARNING
Users must familiarize themselves with the
contents of this manual before using the
MiniOX® 1 Oxygen Analyzer. Failure to do
so can cause misuse of the instrument, and
jeopardize patient well-being.
1-1
Figure 1-1
®
MiniOX
1 Oxygen Analyzer
P/N 474618 [Rev.2] 02/2016
MiniOX® 1 Oxygen Analyzer Section 2, Principal of Operation
Section 2
Principal of Operation
Each MiniOX® 1 Oxygen Analyzer uses a galvanic
oxygen sensor which is long-lived and maintenancefree.
The sensor consists of two electrodes:
• a cathode
• an anode
The gold cathode is exposed to the atmosphere
through a uoropolymer membrane. The lead anode
is submersed in a potassium hydroxide solution.
When oxygen diffuses through the membrane, the
electrochemical reduction of oxygen on the cathode
and the corresponding oxidation of the anode
generate an electrical current. The current produced
is proportional to the partial pressure of oxygen in
the sample atmosphere. The resulting electrical
current is monitored, temperature compensated,
and amplied to drive the display.
The sensor is self-zeroing; when no oxygen is
present to be chemically reduced and oxidized,
minimal current is produced. Thus, zero percent
oxygen is displayed.
stored for a maximum of 6
months without degradation
of life
Response
Time mea-
sured with
deector and
mounted in a
22 mm tee
adapter @
o
25
C
FLOW
RATE LI-
TERS/MIN.
80% OF
CHANGE
(SECONDS)
21321
51220
101119
97% OF
CHANGE
(SECONDS)
Interferent Gases and Vapors
INTERFER-
ENT
%BY
VOLUME
(DRY GAS)
INTERFERENT EQUIVA-
LENT OF PERCENT O
Carbon Dioxide12%<0.1%
Cyclopropane50%<0.1%
Diethyl Ether20%<1.5%
Enurane4%<0.5%
Halothane5%<0.9%
Interferent Gases and Vapors
INTERFERENT
EQUIVALENT
OF PERCENT
O
2
INTERFERENT
% BY
VOLUME
(DRY GAS)
Helium80%<0.2%
Methoxyurane4%<2.3%
Nitrogen80%<0.2%
Nitrous Oxide80%<0.8%
Instrument Replacement Parts
ITEMPART NUMBER
Case Screw637408
Dovetail Mounting Bracket474606
Screws, 4-40x3/8” stainless steel
(set of 4)
450000
Accessories
ITEMPART NUMBER
Alkaline battery, 9-Volt628817
Coiled Cable472045
Deector470687
Home Care Kit (see Appendix A)474682
Mounting Bracket, Pole474664
Mounting Bracket, Wall10023945
Operation Manual CD600700
Oxygen Sensor406931
Sensor Retaining Strap634249
Tee Adapter473021
Operation Manual (Printed)464618
Carrying Case710462
Sleeve Adapter474667
Servicing
Inspection and ServicingSVC-101
2
Cleaning, Calibration and TestingSVC-102
Enclosure ReplacementSVC-103
Circuit Board ReplacementSVC-104
Connector ReplacementSVC-105
3-1
P/N 474618 [Rev.2] 02/2016
MiniOX® 1 Oxygen Analyzer Section 4, Operation
Section 4
Operation
Set-up Procedures
1. Remove the contents from the shipping carton
and verify that you have one each of the following
items:
®
• MiniOX
• 9-Volt Alkaline Battery
• Oxygen Sensor and Deector in Sealed
Package
• 10’ Coiled Cable with twist collar
• Sensor Retaining Strap
• MiniOX
• Tee Adapter
2. Remove the sensor from the sealed package
and attach it to the coiled cable.
• Firmly press the connector until it snaps
into place; tighten the twist collar.
• Insert the opposite end of the coiled cable
into the jack on the side panel of the
instrument; tighten the twist collar.
3. Remove the deector from the package.
1 Oxygen Analyzer
®
1 Operating Manual CD
oxygen concentrations less than 100% or with room
air is less desirable but still acceptable.
1. Press the green ON/OFF button on the front
panel to turn on the instrument.
2. Place the sensor in a ow of air with a known
oxygen concentration or in room air.
3. Wait for a least one minute, or until the reading
has stabilized.
4. If the reading on the display is other than the
known oxygen concentration, adjust the reading
using the calibration dial. Turn clockwise to
increase the reading, or counter clockwise to
decrease the reading.
5. If the reading cannot be adjusted to the known
concentration value, the sensor or instrument is
malfunctioning and must be serviced.
Two-point Linearity Check
The purpose of a two-point check is to determine
the linearity of the sensor. Serious deviation from
linearity (+2%) indicates the sensor is nearing endof-life. To perform a two-point linearity check:
1. Place the sensor in a stream of a known oxygen
concentration between 90-100% until the reading
stabilizes.
• Insert the gasket into the open end of
the deector, ensuring that the gasket is
properly seated within the deector.
• Gently screw the deector onto the sensor.
For monitoring in a breathing circuit, see
Figure 4-1, Sensor Mounting in a Breathing
Circuit.
4. Attach the coiled cable to the instrument in the
same manner.
5. Remove the four screws holding the back panel
in place.
6. Install the battery.
7. Replace the back panel and screws.
8. After installing the sensor, allow to equilibrate
prior to calibration.
9. Proceed to Calibration procedures.
Calibration
The best method to calibrate the MiniOX® 1 Oxygen
Analyzer is with 100% oxygen. Calibrating with
P/N 474618 [Rev.2] 02/2016
2. Calibrate to match this concentration.
3. After calibration, measure room air; the reading
should be 20.8% +2%. (A +2% linearity variation
is allowed for differences due to the method
of sample introduction, the accuracy of gas
concentration, and the precision of initial setting.)
If the variation is greater than 2%, repeat the
two-point linearity check. If the variation remains
greater than 2%, replace the sensor.
Instrument Operation
The MiniOX® 1 Oxygen Analyzer has a low battery
indicator. When the Low Battery indicator is activated,
LO BAT appears on the top left of the display. The
instrument functions normally for approximately
eight hours; however, replace the battery as soon
as possible.
If the sensor becomes disconnected while the
instrument is in use, the instrument displays between
-0.1 and +0.2.
4-1
MiniOX® 1 Oxygen Analyzer Section 4, Operation
The instrument is designed to read in percent from 0
to 100%; however, if incorrectly calibrated, it displays
up to 199.
To maximize battery life, turn OFF the MiniOX® 1
Oxygen Analyzer when not in use.
Sensor Operation
The oxygen sensor has a minimal response to
certain gases other than oxygen. Be aware of these
gases and their interference levels. See Section 3,
Interferent Gases and Vapors.
Coiled
Cable
Sensor
Deector
Tee Adapter
Retaining Strap Installation
To install the retaining strap:
1. Remove the coiled cable from the sensor (Figure
4-2).
Coiled
Cable
Sensor
Tee Adapter
Deector
Sensor
Retaining
Strap
Figure 4-1
Sensor Mounting in a Breathing Circuit
WARNING
The sensor is a sealed unit containing a
potassium hydroxide electrolyte. If the
sensor should develop a leak, discard it
immediately. Should contact occur with skin
or clothing, rinse area with large quantities
of water. In case of eye contact, immediately
ush eyes with water for at least 15 minutes,
holding eyes open. Call a physician.
When using the sensor in a breathing circuit,mount
the sensor with the deector pointing downward
(see Figure 4-1). This prevents moisture from
draining on to the sensor membrane (See Section 5,
Maintenance and Care).
WARNING
Figure 4-2
Retaining Strap Installation
2. Firmly insert the sensor into the tee adapter with
the deector pointing downward; ensure a tight
t exists.
3. Install one end of the strap over a post on the
tee adapter.
4. Loop the strap around the sensor, inserting the
strap center hole over the sensor cable jack.
5. Install the remaining strap end over the other tee
adapter post.
6. Attach the coiled cable to the sensor.
7. Tighten the twist collar.
The sensor is now secured in place.
Effects of Pressure, Humidity and
Temperature
Ensure a tight t exists between the sensor
and the tee adapter. Ohio Medical tee
adapters are engineered to t securely with
Ohio Medical sensors. However, the sensor
retaining strap must be used to prevent
accidental separation of the sensor and tee
adapter.
4-2
P/N 474618 [Rev.2] 02/2016
CAUTION
To ensure accurate and reliable oxygen
analysis, a thorough understanding of
the effects of pressure, humidity, and
temperature on the sensor is necessary.
MiniOX® 1 Oxygen Analyzer Section 4, Operation
Effects of Pressure
The sensor actually senses partial pressure of
oxygen, not percentage. Changes in barometric
pressure changes the reading, even if the percent of
oxygen in the sample remains constant.
Partial pressure of oxygen (PO2) equals the percent
of oxygen (%O2) times (x) the pressure at which the
sample is measured (mmHg-mercury):
PO2 = (%O2) (mmHg)
For example:
At sea level the pressure equals 760 mmHg and dry
air contains 21% O2. Therefore;
PO2 = (21%) (760 mmHg)
PO2 = 160 mmHg
If the instrument is calibrated to read 21% at 160
mmHg partial pressure, then take the instrument
to an area above sea level, where the atmospheric
pressure is 700 mmHg; a lower reading is found due
to a lower partial pressure.
Effects of Humidity
The presence of humidity in an oxygen sample
decreases the actual concentration of oxygen.
Humidity in a sample has the same effects as diluting
the sample with another gas.
For example:
If 100% oxygen is saturated with 100%
humidity, the actual concentration of oxygen
drops from 100% to 96-97%. The instrument
indicates this drop in concentration.
If moisture condenses on the diffusion membrane of
the sensor face, the oxygen path is physically blocked
and a lower oxygen concentration is indicated. This
is typical of all oxygen gas sensors, and is more likely
to occur when the sensor is located downstream
from the humidier. Mount the sensor, when used in
a breathing circuit, so the deector points downward
to prevent moisture from draining onto the diffusion
membrane (see Figure 4-1). Also, mount the sensor,
when possible, upstream of the humidier.
Effects of Temperature
PO2 = (21%) (700 mmHg)
PO2 = 147 mmHg
The percent reading on the instrument is derived by
the following formula:
PO2 Actual = X , 147 mmHg = X or,
PO2 Sea Level 21% 167 mmHg 21%
(21%) (147 mmHg)
(160 mmHg)
X =
Therefore, to eliminate error caused by pressure
changes, the instrument must be calibrated at the
pressure it is to be used.
CAUTION
Do not expose the sensor to pressure
outside the range of 600 to 900 mmHg
(23.62 to 35.43” Hg.) as this can produce
instrument errors.
= 19.3%
Each MiniOX® sensor is desensitized to temperature
changes using a thermistor (temperature variable
resistor) located within the sensor. Variations in the
sensor reading due to temperature changes are less
than 3% when used or calibrated between 0 to 40
degrees centigrade. By using the instrument close
to the temperature at which it is calibrated, variations
can be minimized.
Operating Temperature Range:
0o to 40oC (32o to 104oF)
CAUTION
Do not use instrument outside operating
temperature range.
CAUTION
Do not handle the sensor more than
necessary during calibration or use. Body
heat can cause the sensor’s thermistor to
change disproportional to the change in
gas sample temperature at the sensing
electrode. This can produce some error,
until thermal equilibrium is restored.
P/N 474618 [Rev.2] 02/2016
4-3
MiniOX® 1 Oxygen Analyzer Section 5, Maintenance and Care
Section 5
Maintenance and Care
WARNING
Use only genuine Ohio Medical
Corporation replacement parts when
performing any maintenance procedures
included in this manual. Failure to do
so may seriously impair the analyzer’s
performance. Repair or alteration of the
MiniOX
scope of the maintenance instructions or
by anyone other than an authorized Ohio
Medical Corporation service person could
cause the product to fail to perform as
designed.
Battery Replacement
The MiniOX® 1 Oxygen Analyzer requires one 9-volt
alkaline battery. To replace the battery:
1. Verify the instrument is turned OFF. If it is ON,
press the green ON/OFF button on the front
panel to turn the instrument OFF.
®
1 Oxygen Analyzer beyond the
1. Verify the instrument is turned OFF. If it is ON,
press the green ON/OFF button on the front
panel to turn the instrument OFF.
2. Remove the old sensor from the coiled cable.
3. Attach a new sensor to the coiled cable. Tighten
the twist collar.
4. Recalibrate the instrument. See Section 4, Calibration.
Deector Replacement
To replace the deector:
1. Gently unscrew the old deector and remove
the gasket.
2. Insert a new gasket into the large end of the
new deector. Carefully screw the new deector
onto the sensor, making sure that the new
gasket is properly seated.
See Figure 4-1 for proper sensor and deector
assembly.
Cable Replacement
2. Remove the back panel, which is held in place
by four small screws.
3. Remove and discard the old battery; replace
with a new battery.
4. Replace the back panel and reinstall the screws.
5. Recalibrate the instrument. See Section 4, Calibration.
Sensor Replacement
To ensure safe and effective use of your device, the
sensor must be replaced with a MiniOX
this sensor is manufactured for this instrument. Use
of other types of sensors has not been tested and is
not endorsed by Ohio Medical Corporation. Use of
other sensor types will void your warranty.
There are no serviceable parts in the sensor or cable
assemblies; the entire unit must be replaced.
When the MiniOX
®
1 Oxygen Analyzer is unable to
be calibrated, or gives erratic readings, the sensor
must be replaced. To replace the sensor:
®
sensor as
To replace the coiled cable:
1. Verify that the analyzer is turned OFF. The
display should be blank.
2. Disconnect the old cable from the sensor.
3. Disconnect the old cable from the instrument.
4. Attach the new cable to the sensor. Firmly press
the connector until the sensor snaps into place.
Tighten the twist collar.
5. Attach the new cable to the instrument. Firmly
press the connector until it snaps into place.
Tighten the twist collar.
6. Recalibrate the instrument.
5-1
P/N 474618 [Rev.2] 02/2016
MiniOX® 1 Oxygen Analyzer Section 5, Maintenance and Care
Cleaning, Disinfection and Sterilization
CAUTION
Never autoclave, immerse, or expose the
MiniOX® 1 Oxygen Analyzer (including
sensor) to high temperatures (>70°C). Never
expose the device to pressure, irradiation,
vacuum, steam, or chemicals (other than
alcohol or mild cleaning agents).
Clean the instrument and sensor by wiping with a
cloth lightly dampened with Isopropyl Alcohol or mild
detergent. Make sure that no moisture seeps into
the instrument case or cable jack port.
Instrument
When cleaning or disinfecting the instrument, care
must be taken to prevent entry of solutions into the
instrument case.
Cleaning
The external surfaces of the unit may be cleaned
by wiping them with a cloth moistened with a mild
detergent solution.
Disinfection
The external surfaces of the unit may be disinfected
by wiping them with a cloth moistened with ethanol
or Cidex. The instrument is not designed to withstand
the conditions imposed by steam, ethylene oxide or
radiation sterilization.
Sensor and Cable
Sensor Deector, Retaining Strap and Tee
Adapter
Cleaning
The sensor deector, retaining strap and tee
adapter may be cleaned by wiping them with a cloth
moistened with a mild detergent solution. The parts
must be thoroughly dry before they are used.
Disinfection
The sensor deector, retaining strap and tee adapter
may be disinfected by washing them with ethanol or
Cidex (per manufacturer’s instructions).The parts
must be thoroughly dry before they are used.
Sterilization
The sensor deector, retaining strap and tee adapter
may be sterilized using Cidex (per manufacturer’s
instructions), steam or ethylene oxide. Due to the
varying conditions imposed on materials during
sterilization, it is not possible to determine the exact
number of times sterilization processes can be
carried out. Therefore, the operator must carefully
examine the sensor deector, retaining strap and tee
adapter after sterilization and prior to use to verify
that the item is t for use. The operator must verify
that the items are free from tears and cracks and
that the items have not undergone any materials
changes that may compromise their tness for use
(e.g.,brittleness and dimensional changes). The
operator must also examine the items to verify that
the items are free of chemical residuals resulting
from the sterilization process.
Cleaning
The external surfaces of the oxygen sensor and of
the cable may be cleaned by wiping them with a
cloth moistened with a mild detergent solution.
Disinfection
The external surfaces of the oxygen sensor housing
and of the cable may be disinfected by wiping
them with a cloth moistened with ethanol or Cidex.
The instrument is not designed to withstand the
conditions imposed by steam, ethylene oxide or
radiation sterilization.
P/N 474618 [Rev.2] 02/2016
Because of the variability of cleaning, disinfection and
sterilization processes, Ohio Medical Corporation
cannot provide specic sterilization instructions, nor
can the sterility of an item be ensured
5-2
MiniOX® 1 Oxygen Analyzer Section 6, Technical Information
Section 6
Technical Information
Technical Description
The MiniOX® 1 Oxygen Analyzer is designed to
provide continuous analyzing or spot checking
of oxygen for ventilators, incubators, emergency
transports, and various other respiratory therapy
uses.
Each MiniOX® 1 Oxygen Analyzer instrument uses
an external Galvanic oxygen sensor with its coiled
cord to provide an analog voltage signal proportional
to the percentage of oxygen being sensed.
Oxygen
Cell
Coil
Cord
Fixed Gain
Amplier
A/D Converter & LCD
Driver
The oxygen cell provides an eight (8) to seventeen
(17) millivolt signal (at 20.8% oxygen), which is
amplied by a xed gain instrumentation amplier.
The output of this amplier is fed into a potentiometer
which allows for manual control, by the operator, of
the signal fed to the Analog to Digital/Liquid Crystal
Driver section. The operator will manually adjust
the control in a known oxygen concentration so
the displayed value matches the ambient oxygen
concentration.
Supervisory circuits are present to provide a stable
voltage reference for the A/D circuitry,provide battery
level monitoring, regulators to keep the DC supply
voltages on the devices constant and an ON/OFF
switch press monitor circuit.
Liquid Crystal
Display (LCD)
On/Off
Switch
Regulator
Calibration
Potentiometer
9 Volt
Battery
On/Off Switch
Monitor
A/D Voltage
Reference
Dead Battery
Circuit
Low Battery
Circuit
®
MiniOX
Technical Block Diagram
1
6-1
To Entire
Instrument
Figure 6-1 Block Diagram
P/N 474618 [Rev.2] 02/2016
MiniOX® 1 Oxygen Analyzer Appendix A, Home Care Kit
Appendix A
Home Care Kit
Installation
(Figure A-1)
1. Remove the humidier from the oxygen
concentrator.
2. Thread the universal nipple adapter onto the
oxygen concentrator.
3. Place the sleeve adapter on the oxygen sensor.
CR Oxygen
Analyzer
4. Using the standard oxygen tubing provided,
connect the oxygen sensor to the nipple adapter
on the oxygen concentrator.
5. Proceed to analyze the oxygen concentration.
(Ensure the ow rate does not exceed four liters-
per-minute).
6. When the oxygen analysis is complete, remove
the sampling apparatus and reinstall the
humidier.
Oxygen
Tubing
Oxygen
Concentrator
Sleeve
Adapter
Oxygen
Sensor
Universal
Nipple
Adapter
Figure A-1
MiniOX® 1 Home Care Kit Installation
P/N 474618 [Rev.2] 02/2016
A-1
NOTES:
P/N 474618 [Rev.2] 02/2016
NOTES:
P/N 474618 [Rev.2] 02/2016
Ohio Medical Corporation®
1111 Lakeside Drive
Gurnee, IL 60031 USA
Phone: 1-866-549-6446
Fax: 1-847-855-6218
www.ohiomedical.com
P/N 474618 [Rev.2] 02/2016
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