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Stat Fax 3300 PDF
Stat Fax 3300 PDF
Service Manual
1.1 Applications
1.1.1 Intended Use
This instrument is intended to be used to read and calculate the results of in-vitro
clinical diagnostic assays, as well as any other application requiring absorbance
or concentration readings at or near the available wavelengths. This general
purpose instrument is intended to be used by laboratory professionals capable of
selecting the appropriate features and options for each specific clinical
application.
The design of the instrument includes many features to minimize operator error,
such as stable factory calibration, automatic zeroing, complete operator
prompting, detailed labeling, pre-programmed calculations, visual and audible
feedback, flags and error messages, and minimal maintenance requirements.
The operating modes are: Absorbance Mode, Standard Mode, Rate Mode,
Factor Mode, Multi-point Mode, and Index Mode.
The basic calculations are permanently stored in memory and include several
single and multi-point equations. Provisions are made in certain cases for
reading specimens in duplicate and/or using the mean reading in calculations.
Each calculation mode is described in detail in the Operator’s Manual. These
modes are keyboard selectable and self-prompting to reduce error and simplify
operation.
System Control
The instrument is based on the 8 bit Z180 microprocessor. The software is
permanently stored in a M27C1001 EPROM. A battery-backed non-volatile RAM
(random access memory) chip (MK48T35) incorporating a real-time clock, (2)
24LC515 EEPROM chips are used to store data such as calibration, test setups,
samples, contains 32k of general use RAM, and also maintains the date and
time. All digital I/O is accomplished with (2) 8255 Programmable Peripheral
Interface. Time intervals and pulse widths are measured using the counter
channels of an 8254 programmable timer.
1.2 Specifications
Specification Date......................................21 September, 2002
Model Name ..............................................Stat Fax® 3300
Spectrophotometer Type ...........................Filter photometer
Optical Configuration .................................Single beam with continuously rotating
filter wheel
Monochromatic or bichromatic reading
8 filter positions
Usable Spectral Range..............................330 to 770 nm
System Procedures ...................................Open and by stored menu
Calculating Modes ....................................Absorbance
Single Standard
Differential samples
Factor Mode
Differential samples
Multi Standard Mode (up to 7
standards)
Multi Standard % Abs (up to 7
standards)
Kinetic Mode (consecutively, or
simultaneously (Batch))
By Factor or by Standard
Fixed Time Kinetic
By Factor or by Standard
Index Mode
Channels ...................................................120 Open
Source of Radiation ...................................Tungsten Halogen, 10 Watt, with
automatic lamp saver
Selection of Wavelength ............................By filter
Filter Type..................................................4-cavity interference, long-life ion
beam-assisted deposition
Wavelength Accuracy ................................+/- 3 nm
Filter Location ............................................After sample (heat absorbing filter
before sample)
Filter Selection ...........................................Automatic by software or via keyboard
Wavelengths ..............................................340, 405, 505, 545, 580, 630 nm
supplied standard
other/additional filters optional
Half Bandwidth...........................................< 10 nm
1/100 Bandwidth ........................................14 nm at 340 nm
False Radiant Energy Ratio.......................< 0.001 at 340 and 405 nm
Cuvette ................................................... 1 cm square, 12 cm round, flow through
Supplied Type............................................Flow-through
Material......................................................316 stainless, borosilicate windows
FUSE: For continued protection against the risk of fire, replace only with fuse of
the specified type and current ratings. Disconnect equipment from supply before
replacing fuse.
Read Instructions
Review the following safety precautions to avoid injury and prevent damage to
this instrument or any products connected to it. To avoid potential hazards, use
this instrument only as specified. For best results, familiarize yourself with the
instrument and its capabilities before attempting any clinical diagnostic tests.
Refer any questions to your instrument service provider.
Install as Directed
The Stat Fax® 3300 should be installed on a sturdy, level surface capable of
supporting the instrument’s weight (25 lbs, 11.4 kg) safely for safety and
ventilation purposes. The mounting surface should be free of vibrations.
Use Proper Fuse. Use only the fuse type and rating specified by the
manufacturer for this instrument. Use of a fuse with an improper rating may pose
a fire hazard. Refer to the Power Requirements section for details on fuse
replacement.
Solvents such as acetone or thinner will damage the instrument. Do not use
solvents to clean the unit. Avoid abrasive cleaners; the display overlay is liquid-
resistant, but is easily scratched. The exterior of the instrument may be cleaned
with a soft cloth using plain water. If needed, a mild all-purpose or nonabrasive
cleaner may be used. A 10% solution of chlorine bleach (5.25% Sodium
Hypochlorite) or 70% isopropyl alcohol may be used as a disinfectant. Take
special care not to spill liquid inside the instrument.
Operating Precautions
Be sure to run a sufficient number of controls in each assay. If controls are not
within their acceptable limits, disregard test results.
Biohazard Precautions
BIOHAZARD
A "dead" instrument may result from a blown fuse. However, a blown fuse may
indicate a problem on the main PCB or power supply.
If there is no voltage present at J6, check the fuse located at the back left corner
of the power supply and remove it with a fuse puller, or carefully pry it out with a
small screwdriver. Install a 250V 2A slow blow fuse. Use only the recommended
fuse. Do not substitute other rating! If voltage is present at J6, check for input
voltage on voltage regulators VR2, VR3, and VR4.
For 110-120 V units used in the US, use a UL listed cord set consisting of a minimum 18
AWG, Type SVT or SJT three conductor cord, maximum 3 meters (10 feet) in length,
rated 10 A, 125 V, with a parallel blade, grounding type attachment plug.
For 220-240 V units used inside the US, use a UL listed cord as above, except rated 250
V, with a tandem blade, with grounding type attachment plug. The cord set provided by
the manufacturer meets these requirements.
For other locations, use the power cord certified for the country of use.
Safety Grounding - Do not alter or defeat the safety grounding methods provided. To
avoid the risk of electric shock, the third prong of the AC power plug must be connected
to conductive parts internal to the equipment. Internal fasteners to grounding points are
marked by the IEC 417 symbol 5019. DO NOT loosen or remove these fasteners or
connections. An alternate method of grounding is provided by connecting the grounding
terminal located on the rear panel to a suitable ground.
To avoid electric shock, the power cord protection ground conductor must be connected
to ground.
K
L
I
J
H
G
M
R
T
P S
U
Base. The base supports the rear electronic deck, and is the foundation for the
plate transport and photometer mechanisms.
Port Buffer Board: Contains the parallel, serial, and external keyboard ports. A
cable runs from this board to the Main PCB. The ports use an 8255 located on
the Main Board.
The current configuration (after Revision Level L artwork) of the Surface Mount
Main PCB is as follows:
The 7-segment LED on the Main PCB was replaced by discrete diodes:
D4, D12, D13, D14, and D17 with Revision level L. Figure 2.3.3-1
displays functions as shown and is further described below:
Pump
Tube Detect
Sample Sensor
Valve Action
Cell Heat
Power
• The filter wheel and rotation mechanism: The filter wheel is rotated by
a small DC motor connected to the wheel by a rubber belt. The wheel
speed is electronically controlled to four revolutions per second. As the
wheel turns, the filters mounted in it pass between the light source and
the photo detector, the reading is taken when the filter passes through
the light beam.
• Light source: The light source consists of the lamp with its built-in lens,
the diffuser, and the aperture block. The light, originating at the lamp,
passes through the diffuser, then through the sample plate, the aperture
block, and then into the photometer. This area under the spot of light is
known as the read site. The connection to the lamp and filter wheel motor
is the junction PCB with an IDC (insulation displacement connector.)
Use the home signal to trigger an oscilloscope to observe the test points J8 as
shown above. Each filter peak is sampled and held (U15 Pin 1) and
simultaneously converted from an analog signal to a digital absorbance by an
exponential capacitor decay circuit (U14 Pin 7) and one of the 16 bit counters in
U16 Pin 11. (See the photometer schematic.) The photometer output is
proportional to the power of the light signal whereas the width of the positive
phase of the pulse at the counter chip is proportional to the absorbance. The
resistance (TP1) across the log cap (simple RC decay) determines the base of
the log (10 for absorbance) and is used to adjust the low end absorbance
calibration (gain). Another potentiometer (TP3) is used to null the offset voltages
in the circuits and serves to adjust the hi-end absorbance indications.
Erratic readings (excessive dither) may be a result of trapped air in the Flowcell.
This can be caused by improper installation of, or failure of the Flowcell tubing or
coupling tubes. Refer to the Flowcell Tubing Replacement section. Check the
insertion depth of the Flowcell tubes into the coupling tubes. Ensure that a leak-
free seal is made and that no tubes are kinked or pinched off.
2.3.6 Valve
The valve uses a short length of silicone tubing. If the valve operates but no
sample is drawn up, the pinch valve tubing may be blocked. To check for
clogged valve tubing, unscrew the Flowcell vacuum line from the Luer fitting.
Activate and hold Sample Sensor Optical Switch and listen for aspiration. If you
hear aspiration, the valve is operating, but the Flowcell is clogged. If you do not
hear aspiration, the valve tubing is clogged. Refer to the Valve Tubing
Replacement section.
• Check that the tubing is firmly seated on barbs and all fittings are tight.
Turn the fittings only until finger-tight; do not over tighten the plastic Luer
fittings.
• If the vacuum pump is taking longer to achieve full vacuum (runs much
longer than usual, but otherwise works), the exhaust filter is likely
clogged and should be replaced.
In the event that the exhaust filter gets wet due to a waste bottle spill, it
must be replaced. Reference the Exhaust Filter Replacement section for
instructions on replacing the exhaust filter.
Serial Printer: The Stat Fax® 3300 can print its results out to an Epson
compatible serial printer using the included serial interface port. The data is sent
at 9600 baud, No Parity, 8 data bits, and 1 stop bit. The connection requires a
standard serial cable.
External Heat Block: The Stat Fax® 3300 comes standard with an External
Heat Block. The External Heat Block maintains its temperature at 37.5° C and is
connected to the rear of the Stat Fax® 3300. When active, the temperature is
displayed on screen.
Do not force the cover backwards. Damage to the cover or fittings may result.
To reinstall the cover, reverse the procedure. Carefully lower the cover until it
seats on the chassis, taking care to clear the incubation block and the Flowcell
Luer fitting.
Pump
Valve
Photometer Fan
Proper cleaning will help to prevent clogging of the Flowcell tubing and valve
tubing. Cleaning is extremely important to obtaining accurate, repeatable results.
If reagent, serum, or other proteinaceous fluid is allowed to dry in the Flowcell, it
is extremely difficult to remove and its presence can affect test results.
4. Aspirate 0.1N hydrochloric acid (HCl). Allow the solution to remain in the
Flowcell for 3 minutes.
6. If the Flowcell is to be removed for storage, purge with air until no more fluid
can be seen flowing into the waste bottle. Otherwise, leave the Flowcell filled
with water.
Current Flowcell STATUS = ON OFF The current status of the Flowcell will
be highlighted (ON or OFF).
Current Aspiration VOLUME = 500 µL
Press the F1 key to toggle the
Flowcell Mode ON
The screen will display the current aspiration volume. Current Aspiration VOLUME =
NOTE: When reading sample in Flowcell Mode, remember to have more sample than the
aspiration volume selected. Attempting to aspirate the exact amount of sample may result in poor
results due to air mixing with sample. User technique, the shape of the bottom of vessel being
used, and the location of the tube during sampling can affect this process.
FLOWCELL CALIBRATION
Enter Menu Number:
1 = Read Water Reference
2 = Flowcell Alignment A short description of each option
follows below.
QUIT
Press:
The instrument references water instead of air when reading with the Flowcell. These
reference values are stored in non-volatile memory and used whenever the Flowcell is
active and until new values are read. This should be done before Flowcell Alignment.
In order to insure good blanks when using the Flowcell, conduct Read Water Reference on
a regular basis; time intervals depend upon instrument usage and when encountering
unexpected (very high, very low) blank values.
Necessary when a new Flowcell is used, or if a lamp replacement has occurred. Conduct
Read Water Reference before and after Flowcell Alignment.
The Flowcell should be active but NOT inserted into the read well.
– Submerge the end of the tubing into a container of water and activate the Sample
Bar. Continue with the interruption of the beam until water starts to flow into the
Waste Bottle. This will decrease the likelihood of air bubbles interfering with an
accurate reading.
– This reading should be slightly over half of the original reading. If it is not, the
Flowcell must be adjusted.
– If the displayed value is less than 50% of the reading with the Flowcell removed,
purge and remove the Flowcell.
– Adjust the set screw with the hex wrench supplied. Turn the set screw 1/4 turn in
either direction and replace the Flowcell.
– Sample water again. If the value increases, turn the set screw in the same
direction. If the value decreases, turn the setscrew in the opposite direction.
– When complete, press QUIT to return to the main prompt. New water values must
be read as described above in Read Water Reference.
The Flowcell alignment instructions can be found above in Section 3.3 Flowcell
Configuration.
The Flowcell utilizes 1.2mm I.D. Teflon tubing for the Inlet (sample) and Exit tubes.
Replacement tubing is included with the tubing kit. Follow this procedure to replace the
Flowcell tubing.
Materials/tools required:
Flowcell handle
Flowcell handle
Remove the
retainer plate
from the
Flowcell
handle by
removing the
two flathead
screws.
Retainer plate
• Remove the Exit tubing (reference Figure 3.5D) at the metal tube and pull
it through the Flowcell handle. Slip the Inlet tubing out and away from the
Flowcell handle.
• Remove the two pan head screws with split lock washers from the underside
of the retainer plate (reference Figure 3.5E) and slide off the retainer plate.
Figure 3.5E Remove two pan head screws with split lock washers
• Remove the upper cell body from the lower cell body assembly by removing
the two flat head machine screws from both sides of the upper cell body (see
Figure 3.5F). Once the screws are removed, pull the upper cell body apart
from the lower cell body assembly.
Remove the
four flathead
screws from
the lower cell
body retainer
plate.
• Once the cell retainer plate is removed, lift off the cell window and the seal to
access the metal cell insert. Grasp the cell insert and lift it out from the lower cell
body.
• Remove the Inlet (sample) tubing from the steel tube on the cell insert. Remove
the ground contact sleeve from the metal tube.
• Locate the Inlet (sample) tubing from the tubing kit. Carefully press the end of
the Inlet tubing (the swaged end) onto the short steel tube of the cell insert.
Read the tip that follows for immobilizing the glass cell window to make
reassembly easier.
¾ Ensure that an o-ring is inserted into the cell retainer plate (reference
Figure 3.5H).
¾ While holding the remaining glass cell window by its edge with
tweezers, dip the remaining glass cell window in isopropyl alcohol (this
will help immobilize the cell window for ease in placement) and place it
in position on the underside of the cell retainer plate.
¾ Insert two of the screws into the cell retainer plate at opposing corners
and set the cell retainer plate into position and tighten the screws.
• Once the lower cell body is assembled, attach the upper cell body to the lower
cell body assembly by slipping the Inlet tubing and metal cell insert through the
center hole of the upper cell body. Push the two pieces together until they are
flush. Reinstall the two flathead machine screws to each side of the upper cell
body to hold the upper cell body and the lower body cell assembly together
(reference Figure 3.5F and Figure 3.5I).
Figure 3.5I Upper cell body and lower cell body assembly
• Slide the Inlet tubing and metal insert through the center hole on the retainer
plate (reference Figure 3.5E).
• Insert the ground contact sleeve over the metal cell insert tube (reference
Figure 3.5J) pressing it into place until the ground contact sleeve is at the
height of about 1/8”.
Underside of
retainer plate
with the two
pan head
screws with
split lock
washers in
place
Metal cell
insert for exit
tube with
ground contact
sleeve in place
• Feed the Exit tube through the hole provided in the Flowcell handle (reference
Figure 3.5D).
• Feed the Inlet tube into the Inlet (sample) tube support via the hole provided
inside the Flowcell handle.
• Attach the Exit tubing to the metal cell insert (reference Figure 3.5D).
• Carefully, without kinking the tubing, snug the Exit tubing and the Inlet tubing into
place such that the retainer plate can be fastened to the Flowcell handle.
• Reinstall the two flathead machine screws (reference Figure 3.5C) to hold the
retainer plate and assembly to the Flowcell handle.
• Follow the process for testing for leaks in the Flowcell assembly.
FLOWCELL CALIBRATION
Enter Menu Number: Numeric key 2
1 = Read Water Reference
2 = Flowcell Alignment Flowcell Alignment
QUIT
Press LINE FEED twice to advance the paper feed so LINE FEED
that the reading is visible.
LINE FEED
Install the Flowcell into the photometer. Snug the Exit
tubing into the Flowcell Luer fitting (do not over tighten).
Press and hold in the Sample Bar until there are no air
bubbles visible in the Exit tube feeding into the Waste
bottle.
To replace the cell insert, follow the instructions on disassembling the Flowcell in
Section 3.5 Flowcell Tubing Replacement. Once the lower cell body assembly is
disassembled, remove the cell insert and install the new cell insert. Assure the
correct orientation is used when installing the new cell insert by following the
illustration in Figure 3.5H. Reassemble the Flowcell following the instructions in
Section 3.5 Flowcell Tubing Replacement. Use the procedure provided to check
for possible leaks in the Flowcell.
2. NOTE: For ease of relocating for reassembly, mark the chassis with a pencil
along the front and side edges of the photometer subassembly as shown
below.
3. Locate the two #6 screws holding the photometer assembly to the chassis.
From the bottom of the instrument, remove these screws, washer, and the
speed nuts from inside the instrument.
NOTE
The internal tooth lock washer must make electrical contact (ground) with
the chassis base for low noise operation.
2. Refer to Figure 3.6.2. Remove the four screws securing the Main PCB.
Secure the replacement PCB in the same fashion as the removed PCB.
Set the power switch to OFF (O). Open the instrument as described in
Section 3.1 Opening the Instrument. Refer to Figure 3.1. Locate the valve.
Refer to Figure 3.9. Pull back the pinch bracket and remove the valve tubing
from the valve body.
Push the tubing over the tubing barbs until seated. Be especially careful not to
kink, stretch, or tension the tubing.
2. Locate the EPROM socket (see Figure 3.10.2) and push the small blue
levers outward at both ends of the socket (see Figure 3.10.3). This frees the
EPROM for easy removal and insertion.
3. If necessary, gently bend the pins of the new EPROM so that the pins are
perpendicular to the EPROM (see Figure 3.10.1). Hold the EPROM by the
body and bend the pins against a flat surface such as a table to bend all
the pins the same amount. Do not over bend the pins, since they are easy to
break if bent too far.
4. Install the EPROM with the notch oriented as shown in the label on the
EPROM socket. The notch should face toward the left side of the
instrument. Figures 3.10.2 and 3.10.3 display the location of the EPROM
on the Main PCB and an enhanced view of the EPROM label showing the
direction of the arrow for proper orientation.
5. Reinstall the cover and power cord. Turn the instrument back on.
Note the
direction of
the arrow on
the EPROM
label for
proper
orientation.
Materials/tools required:
1. Disconnect the unit from the AC power source and detach the power cord.
Open the instrument (see Section 3, Service Procedures). Set the cover out
of the way.
2. Locate the photometer. Unplug the 4 pin lamp/motor cable from the
interconnect printed circuit board (PCB). Using the flat blade screw driver,
unplug the gray cable from the interconnect PCB.
3. IMPORTANT: Refer to Figure 3.1. Follow the procedure in Section 3.8 Main
PCB and/or Photometer Replacement for removing the photometer.
4. Remove the four 6-32 screws retaining the photometer cover. Set the cover
aside. Remove the two 4-40 screws securing the photometer PCB. Remove
the drive belt from the filter wheel. Using the blade screwdriver, remove the
filter wheel shaft. Remove the wheel. Remove the shaft taking care not to
misplace the nylon spacer/washers.
6. There are two means of filter retention in field use; silicone glue or a retaining
ring. If a retaining ring is used, carefully pry two to three of the retaining ring
teeth away from the filter until the ring is dislodged and remove the ring and
filter. If silicone glue is present, remove the silicone and push the filter from
the wheel using the eraser end of a pencil or other soft blunt object and any
residual glue should release. Remove any neutral or screen disks that may
remain in the filter cavity.
7. Locate the neutral filters and/or screens that were included with the
replacement filter and drop them first into the cavity. Next insert the filter with
the mirror side down. Place the replacement retainer over the filter so that the
tabs are angled away from the filter and press in place with a 7/16 diameter
wooden dowel or similar object.
8. Reinstall the filter wheel on the bracket taking care not to pinch any washers
under the shoulder of the shaft. Tighten the shaft. Replace the belt. Replace
the photometer PCB taking care to center the board around the shaft.
Tighten the two 4-40 screws. Replace the optical cover taking care to
position the gray cable in the slot of the cover. Do not pinch the cable
under the cover. Insert the three 6-32 screws and snug up. Do not over
tighten.
10. If necessary refer to the lamp alignment procedure in the service manual.
11. Plug the cover cable back into the main PCB. Replace the cover but do not
install the cover screws. If an updated EPROM was included with the filter
replacement kit, install it now referring to the EPROM replacement sheet.
12. Attach the power cord and connect the unit to the AC power source. Turn the
unit on. The displayed numbers represent the voltages of the installed filters.
All voltages should be between 2 and 10 volts. To terminate this mode, press
Clear as required.
NOTE: If the filter voltage is not in the range specified in the previous step,
check lamp alignment. If the lamp alignment is properly set, the neutral
density filters may need to be changed. Add neutrals to lower the voltage.
Remove neutrals to increase the voltage. Never adjust the trim pots on the
main PCB to obtain the correct voltage. Refer to Section 4 Troubleshooting
as needed.
13. Detach the unit from the AC power source. Replace the two cover screws. Refer
also to Section 3.12 Lamp Replacement and Section 4 Troubleshooting.
Remove retainer
(if used), filter,
and neutrals with
soft, blunt object.
Two Nylon
Washers
Install replacement
neutrals, filter, and One Nylon
retainer using 7/16 Washer
dowel.
Locate the photometer and the lamp at the right side of the photometer. Refer to
Figure 3.12-1 Lamp Replacement. The figure shows the right side view of the
photometer assembly.
Avoid handling with bare skin. Insert the lamp leads into the connector until they
hit bottom. Refer to Figure 13.12-2, for proper lamp alignment. The lamp filament
must be centered on the lens and the lamp body must be parallel with the lens
bracket. While holding the lamp in alignment, tighten the lamp connector screws.
Set the power switch to ON. Observe the projection of the light from the lamp
onto the cell holder (behind the lens). Refer to Figure 3.12-2 for spot alignment.
The spot should be small and centered on the oval hole in the cell block (behind
the lens). If the spot is not centered, use the adjustment screws to position the
spot. The vertical adjustment screw raises and lowers the lamp bracket. The
lamp bracket is slotted at the horizontal adjustment screw, so that the lamp
bracket can be moved. The horizontal adjustment screw serves to lock down the
lamp bracket.
Insert a borosilicate 12 mm tube filled with plain water into the read well. Do not
use a soda-lime glass tube, since it does not transmit at 340nm. Press F4
(TOOLS). Press 4 and ENTER. Press 1 and Enter. The display shows the
voltages for each filter.
X X
Correct Incorrect Incorrect
Vacuum gauge
• Select F4 OK
• Press and release the Sample bar. The vacuum gauge should read 7.0 ±
0.5. If not, adjust trim pot TP2 until the reading on the vacuum gauge is
within the acceptable range. When the reading on the vacuum gauge is
within the acceptable range, remove it and connect the vacuum line to
the instrument at the blue fitting.
• Perform Self Check by selecting the TOOLS Menu F4; select Diagnostics
Menu numeric key 4; select Self Check numeric key 6, and check that the
vacuum system reading displayed is OK, select F1 to Quit.
System Diagnostics:
EEPROM OK
NV RAM OK
Vacuum System OK
Aspiration Valve OK
Photometer OK
______________________________________
QUIT REPEAT ENTER
• Before uncoupling the exhaust filter from the Inlet tubing, note the
orientation of the wording (INLET) on the exhaust filter. The side of the
exhaust filter with the wording (INLET) should face away from the blue
vacuum fitting (see Figure 3.14-1).
• Install the new filter with the INLET side pointing away from the blue vacuum
fitting. Push the tubing on the fitting until seated.
Exhaust
filter
Inlet
wording
Vacuum
fitting (blue)
Figure 3.14-1 Exhaust Filter
• Check that the tracks are covered down to the insertion point. If the
covering has been damaged, insulate it with clear tape.
• If the problem still persists, massage over the keypad until the beeping
starts. If necessary, stick the key with a pin to equalize the air pressure
inside. If necessary, replace the keypad. If the tracers on the key tails
are missing conductive material at the end that plugs into the interface
PCB, the insulation may be trimmed back 1mm at a time to expose fresh
contact material.
NOTE: To avoid the “stuck key” scenario, it is Important that the key be
pressed for a very short duration, such as five beeps maximum.
• The password control window will display the status of the password; the
status can be changed from ON to OFF.
• Insert a borosilicate 12 mm tube filled with plain water into the read well.
Do not use a soda-lime glass tube, since it does not transmit at 340nm.
• Press F4 (TOOLS).
• The display shows the voltages for each filter. Make sure that all are
greater than 2 volts. If a particular channel is low, the filter may be
degrading. Ensure that the lamp is fine and that there is nothing blocking
the light path such as dirt or dust. Replace if less than 1 volt.
• If the filter wheel motor is running, but the filter wheel does not seem to
be rotating, check the two rubber belts.
• If the motor is not turning, check that the motor has between +5 and +6
volts across the motor terminals. (Make sure that the reader is attempting
to read a plate or running test 186.)
• Also check that the wheel home pulse is arriving at the 8255 port, PC6
pin 11.
• If neither are present and the cables are installed correctly, check the IR
LCD pair on top of the photometer housing for 1.2 to 1.5 volts between
the black and the white wire. A reading of +5 volts here indicates an open
LCD or unterminated return.
• Be sure that the appropriate wavelengths were selected for the chromophore
being read.
4.2.8 No sampling
• If you can hear the valve cycle, but no sample is drawn up, the valve tubing may
be blocked. Press and hold PURGE several times. Disconnect the Luer fitting at
the rear of the Flowcell. Press PURGE and listen for aspiration. If air is heard
entering the fitting, the valve tubing is clear, but the Flowcell is blocked. Refer to
the Flowcell Cleaning section and the Flowcell Tubing Replacement section.
• If the valve clicks but the pump does not run when you activate the
Sample Switch, the valve tubing may be stuck closed. If this happens,
remove the front cover screw and lift open the cover. Pull the pinch
bracket against the spring tension (to open the valve manually). Gently
pull the tubing slightly to break the seal. See the section titled Valve
Tubing Replacement for a diagram and more information about the valve
tubing.
The temperature calibration data is stored as offsets which the instrument adds
to the sensed temperatures. The absorbance calibration data is stored as a
scaling factor, which is the ratio of a known reference absorbance to the
instrument's reported absorbance. The calibration data may be printed at any
time by selecting test #213. This prints the serial number of the instrument, the
date of last calibration, and the stored calibration data for the absorbance and
cell temperature.
The calibration data is stored with a check sum that is recalculated and
compared each time a mode is selected. Failure to recover the calibration data
properly (checksum failure) will be indicated on the display and the internal
printer:
Do Temperature Calibration Test
The instrument annunciates this condition with multiple beeps. The temperature
offset for the read well is then set to 0.0 and the absorbance scaling factor is set
to 1.000. In this condition, the maximum temperature error is ±1.5 ½C and the
maximum absorbance error is ±10%. The calibration data can be restored as
described in “Restore calibration”.
Changing these settings will make the factory calibration data invalid.
Do not enter values other than those recorded on the calibration label
unless absolutely necessary.
Changing these settings will make the factory calibration data invalid.
Do not enter values other than those recorded on the calibration label
unless absolutely necessary.
1. Shut off the instrument. Remove any tubes or cuvettes from the read well.
Carefully lift up the instrument and locate the Calibration Data label on the
underside of the unit. There are (2) values recorded there: Absorbance and
Cell Temp. Write down these numbers.
3. If the date and time have been reset or are incorrect, enter the correct date
and time. See the section “Set Date and Time” in the Operator’s Manual.
4. Press TOOLS (F4). Press 4 and Enter. The Diagnostics Menu is shown.
Choose 3 for Absorbance Calibration and Enter. Enter the Number.
6. Press Run Test (F1), type in 213, and press ENTER to get a report of the
calibration data. The cell temperature adjustment will be printed along with
the absorbance adjustment. Make sure that these values are the same as
those recorded on the calibration label.
• 12 mm borosilicate tube
Temperature calibration:
2. Remove the Flowcell and install the Temperature Calibration Fixture into the
read well.
4. Set the DMM to read 20K. Read the resistance of the Thermistor and the
fixture. If the resistance is between 17724 ý and 18712 ý, no adjustments
are needed. Otherwise, continue to the next step.
T = R - 18210
Where:
Cell adjust=
Type the offset calculated for the cell and press ENTER. The maximum
allowed adjustment is ±3.0C . Entering values that exceed this net number
will produce an out of range message.
8. Select test #213 to see the current net adjustments. Record the new values
on the calibration label located on the bottom of the instrument.
• 12 mm borosilicate tube
• Reference spectrophotometer
2. Place a 12 mm borosilicate test tube filled with 1 ml of water into the read
well.
3. Select TOOLS, Diagnostics, FILTER VOLTAGES. Confirm that all of the filter
voltages are between 2.00 and 10.00 volts. Refer to Section 4.2 Photometer
Problems if voltages are not within this range.
Never adjust trim pots on the Main PCB to achieve the proper voltages.
5. Remove the tube and install the Flowcell in the instrument. Press Program to
create an ABS test. Select the required wavelengths. Blank on the same
diluent material used to prepare the concentrations.
6. Read the 1:2 dilution. Divide the absorbance as read on the reference
spectrophotometer by the reported absorbance value.
7. Exit the absorbance mode by pressing QUIT to return to Main Menu. Press
TOOLS, DIAGNOSTICS, Absorbance Calibration. At the prompt
“Absorbance factor= x.xxx?”, enter the ratio calculated. When this factor is
entered the instrument will display a net factor (the new calibration data).
8. Press QUIT and restart the absorbance mode. Blank as before on the
diluent. The 1:2 dilution absorbance should now agree with the reference to
within +/-.005 absorbance.
9. Read the 1:1 concentration. It should agree within +/-2 % of the reference. If
necessary, carefully adjust trimpot TP3 to achieve this agreement. Re-blank
and reconfirm the values.
10. Select test #213 to print the new calibration data. Enter these values on the
calibration data label on the bottom of the instrument.
Filter labels need to be re-entered for two of the filters. Open the instrument and locate
the filter label on the side of the photometer cover.
Key 7 is xxx
Key 8 is xxx
Where “xxx” is a three-digit wavelength value. If there are no 7th or 8th filters, they will be
listed as BLOCKED. Press RUN TEST (F1), type in 248, and press ENTER. The display
prompts:
Key 7 = ??? nm
Type in the wavelength for Key 7 that is printed on the label and press ENTER. Repeat
for Key 8. use “000” for unused filter positions. Press QUIT to return to the main prompt.
Note that, if values for Key 7 and Key 8 are entered when there are no filters present, the
filters will be flagged as “low” when Self Check is run.
If you continue to have problems after consulting your dealer, contact the factory.
E-mail: support@awaretech.com
USA
When contacting us, please have serial number of the Stat Fax® 3300 in
question. Have a description of the problem with as much detail as possible.
Save any relevant jobs or logs to disk and send or e-mail us the information.