Research Instruments RI WITNESS User manual

User Manual
Document 6-70-807UM, Issue P1, 18 February 2016
RESEARCH INSTRUMENTS LTD
Bickland Industrial Park, Falmouth, Cornwall TR11 4TA, UK
t: [phone] | f: [phone] |e: [e-mail]
www.research-instruments.com
RI WITNESS™
0120
Embryology Heated Plate
only

CONTENTS
 
 
Indicaons for Use for RI Witness Embryology Heated Plate 2
Applicable Part Numbers 2
Related Documents 2
Compability 2
Installaon 2
 
Guidance and Manufacturer’s Declaraon (Part 15 of FCC)
— Electromagnec Emissions 4
Guidance and Manufacturer’s Declaraon (IEC 60601-1-2)
— Electromagnec Emissions 4
— Electromagnec Immunity 5
— Electromagnec Immunity 6
Safety/Informaon Symbols 7
Safety and Reliability 8
Temperature Safety 8
RFID Reader Environment 8
Startup / Shutdown Procedure 8
 
Embryology Heated Plate 9
RI Witness Embryology Heated Plate Specicaon Table 10
 
Startup Procedure 11
Shutdown Procedure 11
Connecng to the Soware 11
User Interface 11
Achieving the Correct Sample Temperature 12
Changing the Temperature Setpoint Using the Device 13
Changing the Temperature Setpoint using a PC and RI Witness Work Area soware 13


Temperature Calibraon 14
ITO Glass Window Calibraon Using Built-In User Interface 14
Full 5-channel Calibraon Using PC and RI Witness Work Area Soware 15
Tube Reader Antenna Accessory 16
 
Alarms and System Status 18
Audible Alarms 18
Alarm Condions Codes 19
 
Cleaning 23
 
Reuse Statement 24
RI Repairs System 24
Product Disposal (European Union) 24
RI Returns System 24
Contact Details 24
Obligaon to Inform 24
Feedback 24
CONTENTS


Secon 1
1
1

Preface

Thank you for choosing RI Witness.
This manual provides all necessary informaon to use RI Witness Embryology Heated Plate and
should be read in conjuncon with any manuals provided with other RI Witness hardware or soware
components that you are using. The system should be operated by trained personnel only. All secons
of this manual should be read and understood fully before any operaon of the system. Please see the
Intended Use for more informaon.
If the operator is unsure of any of the informaon contained in this manual they should contact Research
Instruments or an appointed representave before aempng to use this equipment.
In no event does Research Instruments Ltd (RI) assume the liability for any technical or editorial errors
of commission, or omission; nor is RI liable for direct, indirect, incidental, or consequenal damages
arising out of the use or inability to use this manual.
The informaon in this manual is current at the me of publicaon. Our commitment to
product improvement requires that we reserve the right to change equipment, procedures
and specicaons at any me. The latest version of the User Manual can be downloaded from
soware.research-instruments.com. The RI Witness manual belongs with the RI Witness system and
should be passed on with the system if relocated to another clinic.
The use of ™ in this manual indicates a trademark of Research Instruments Ltd. Any other brand names,
referred to in this manual, are trademarks of their respecve owners.
© This manual is protected by copyright, all rights reserved, and no part here of may be photocopied
or reproduced in any form without the prior wrien consent of RI.
             



Secon 2
2
Introducon

2


To maintain the temperature of human reproducve ssue such as oocytes and embryos through an
assited reproducon (AR) cycle.
Applicable indicaons for use are subject to the regulaons of the country into which the device is sold.
Availability of RI Witness for clinical use is dependent on the regulatory approval status of RI Witness
within the country the device is intended to be sold into.


6-7-121UM RI Witness Soware Manual

RI Witness is used in conjuncon with the following:
• Essenal medical devices, eg dishes and tubes, maybe AR or non-AR specic.
• Non-essenal medical devices, eg safety cabinets, incubators, micromanipulators, lasers.
• Non medical devices (general laboratory equipment), eg work benches, microscopes, PCs.
This device is not intended to be exposed to known sources of electromagnec Interference (EMI) with
medical devices such as diathermy, and electromagnec security systems e.g., metal detectors and
electronic arcle surveillance system.

Installaons of the RI Witness Embryology Heated plate should be carried out by a RI technician or
other RI authorised personnel. Incorrect installaon could result in overall poor performance.
 
6-70-807* RI Witness Embryology Heated Plate
6-70-809 RI Witness Tube Reader
* 6-70-807 can be supplied in several conguraons depending on the required mounng type eg ush
ed or sit on top.
0120
only

Secon 3
Safety Warnings
3

3

disassemble or modify any part of the RI Witness Embryology Heated plate, or
substute any component for any other. Doing so may result in damage to samples. This
voids the warranty and/or service contract.
 To avoid the risk of electric shock, this equipment must only be connected
to a supply mains with protecve earth.
 use the power cable and power supply adaptor supplied with the system.
The cable to the power supply is the ‘disconnect device’ for this equipment. To remove all
electrical power from this product, disconnect the power cable from the electrical outlet.
Equipment should be posioned so as to allow easy access to the power cable. The appliance
coupler or mains plug is used as the disconnect and must remain readily operable.
Not to be used in a paent environment.
The system should be operated by qualied and trained personnel only.
This symbol indicates cauonary text which should be followed to avoid injury to users
or damage to samples.

Secon 3
4
Safety Warnings

3
RI Witness is intended for use in the electromagnec environment specied below. The customer or
the user of RI Witness should ensure that it is used in such an environment.


  
RF emissions
CISPR 11 Group 2
RI Witness must emit electromagnec energy in
order to perform its intended funcon. Nearby
electronic equipment may be aected.
RF emissions
CISPR 11 Class B
RI Witness is suitable for use in all establishments
other than domesc and those directly connected
to the public low-voltage power supply network
that supplies buildings used for domesc
purposes.
Harmonic emissions
IEC 61000-3-2 Not applicable
Voltage uctuaons/
icker emissions
IEC 61000-3-3
Not applicable


 This equipment has been tested and found to comply with the limits for a Class A digital device,
pursuant to part 15 of the Federal Communicaons Commision (FCC) Rules. These limits are designed
to provide reasonable protecon against harmful interference when the equipment is operated in a
commercial environment. This equipment generates, uses, and can radiate radio frequency energy and,
if not installed and used in accordance with the instrucon manual, may cause harmful interference
to radio communicaons. Operaon of this equipment in a residenal area is likely to cause harmful
interference in which case the user will be required to correct the interference at their own expense.
 This device complies with Industry Canada’s licence-exempt RSSs. Operaon is subject to the
following two condions:
1. This device may not cause interference.
2. This device must accept any interference, including interference that may cause undesired operaon
of the device.

Secon 3
Safety Warnings
5

3


 

 

Electrostac discharge
(ESD)
IEC 61000-4-2
± 8 kV contact
± 15 kV air
± 8 kV contact
± 15 kV air
Floors should be wood,
concrete or ceramic le.
If oors are covered
with synthec material,
the relave humidity
should be at least 30%.
Electrical fast transient/
burst
IEC 61000-4-4
± 2 kV for power supply
lines
± 1 kV for input/output
lines
± 2 kV for power
supply lines
± 1 kV for input/
output Lines
Mains power quality
should be that of a
typical commercial or
hospital environment.
Surge
IEC 61000-4-5
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
± 1 kV dierenal
Mode
± 2 kV common mode
Mains power quality
should be that of a
typical commercial or
hospital environment.
Voltage dips, short
interrupons and voltage
variaons on power
supply input lines
IEC 61000-4-11
<5 % UT
(>95 % dip in UT ) for
0.5 cycle
40 % UT
(60 % dip in UT) for 5
cycles
70 % UT
(30 % dip in UT) for 25
cycles
<5 % UT
(>95 % dip in UT)
for 5s
<5 % UT
(>95 % dip in UT ) for
0.5 cycle
40 % UT
(60 % dip in UT) for 5
cycles
70 % UT
(30 % dip in UT) for 25
cycles
<5 % UT
(>95 % dip in UT)
for 5s
Mains power quality
should be that of a
typical commercial or
hospital environment.
If the user of RI Witness
requires connued
operaon during power
mains interrupons, it
is recommended that
RI Witness be powered
from an uninterrupble
power supply or a
baery.
Power frequency
(50/60 Hz)
magnec eld
IEC 61000-4-8
3A/m 3A/m Power frequency
magnec elds
should be at levels
characterisc of a
typical locaon in a
typical commercial or
hospital environment.
UT is the a.c. mains voltage prior to applicaon of the test level.

Compliance with the emissions requirements of CISPR 22 Class A requires the following warning:
“This is a class A product. In a domesc environment this product may cause radio interference in
which case the user may be required to take adequate measures.”

Secon 3
6
Safety Warnings

3
 





Conducted RF IEC
61000-4-6
Radiated RF IEC
61000-4-3
3 Vrms
150 kHz to 80 MHz
3 V/m
80 MHz to 2.5 GHz
3 Vrms
3 V/m
Portable and mobile RF communicaons
equipment should be used no closer to
any part of RI Witness, including cables,
than the recommended separaon
distance calculated from the equaon
applicable to the frequency of the
transmier.
Recommended separaon distance
d = [3.5/V 1] √p
d = [3.5/V1] √p 80MHz to 800MHz
d = [3.5/V1 √p 800MHz to 2.5GHz
where pis the maximum output
power rang of the transmier in
was (W) according to the transmier
manufacturer and dis the recommended
separaon distance in metres (m). Field
strengths from xed RF transmiers,
as determined by an electromagnec
site survey, a should be less than the
compliance level in each frequency
range. bInterference may occur in the
vicinity of equipment marked with the
following symbol:
At 80 MHz and 800 MHz, the higher frequency range applies.
 These guidelines may not apply in all situaons. Electromagnec propagaon is aected by
absorpon and reecon from structures, objects and people.
 These guidelines may not apply in all situaons. Electromagnec propagaon is aected by
absorpon and reecon from structures, objects and people.
a Field strengths from xed transmiers, such as base staons for radio (cellular/cordless) telephones
and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theorecally with accuracy. To assess the electromagnec environment due to xed RF transmiers,
an electromagnec site survey should be considered. If the measured eld strength in the locaon
in which RI Witness is used exceeds the applicable RF compliance level above, RI Witness should be
observed to verify normal operaon. If abnormal performance is observed, addional measures may
be necessary, such as re-orienng or relocang RI Witness.
b Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than [V] V/m.



Secon 3
Safety Warnings


3

 
Indicates instrucon for disposal of goods.
In accordance with Annex II of the European
Medical Device Direcve 93/42/EEC, as amended
by Direcve 2007/47/EC under the supervision of
noed body No.0120, SGS, UK Ltd.
In accordance with the European Direcve for
R&TTE, Direcve 1999/5/EC
Indicates the medical device manufacturer.
Indicates the date of manufacture.
Indicates the need for the user to consult the
instrucons for use for important cauonary
informaon such as warnings and precauons that
cannot, for a variety of reasons, be presented on
the medical device itself.
Consult instrucons for use.
The four digit number is a unique idener
assigned to the product.
Cauon: US Federal law restricts this device for
sale to or on the order of a licensed healthcare
praconer.
S
N
Only

Secon 3
8
Safety Warnings

3

Please read this manual carefully and follow the instrucons to ensure that the system will work safely
and reliably.

Safety is the responsibility of the laboratory. Risk assessment and working pracces should comply with
local regulatory policies.
A warning triangle will be displayed on the work area touch screen and the status LED on the device
user interface will display a yellow status alarm if the currently selected temperature cannot
be maintained.
Gently place your hand on the heated surface to verify that the temperature is appropriate for use.
As with all heang systems, it is advisable to perform a periodic check of temperatures using a calibrated
thermocouple thermometer.

An RI Witness system uses Radio Frequency Idencaon (RFID) readers to monitor a work area.
Readers detect RFID tagged containers that are placed in the work area.
The performance of RFID tag detecon may be compromised by reposioning the reader and by the
proximity of metal objects or electrical equipment that were not present during installaon and tuning.
If the device is relocated ensure that the autotuning procedure documented in the RI Witness Soware
Manual (6-7-121UM) is followed to ensure opmum level of performance.
For cleaning the reader may be lied and returned to the same posion. See “Cleaning” on page 23
for more cleaning details.





RI Witness hardware may be damaged by incorrect startup and shutdown procedures.
“Secon 5 - RI Witness Basic Operaon” on page 11 describes the recommended startup and
shutdown procedure for the RI Witness Embryology Heated Plate.

Secon 4
Product Overview


4

RI Witness is a system which operates within an assisted reproducon (AR) clinic seng and provides
a method of idenfying human samples throughout an AR cycle (from egg and sperm collecon to
embryo transfer). The system is intended to minimise the risks associated with tradional/manual
double-checking and provides the essenal controls necessary to ensure eggs, sperm and embryos are
correctly matched and treated during the AR process.
The RI Witness system comprises hardware, rmware and soware components, which can be
congured depending on the treatment acvies, number of AR cycles conducted, size and layout of
the AR clinic.
RFID (radio frequency idencaon) technology provides the means of idenfying the containers
(dishes, tubes) in which eggs, sperm and embryos are transferred and stored. The containers are
labelled by a clinician with a special RFID tag which has been assigned a unique idener. The unique
idener is linked to a paent/couple (specic parentage).
As samples are processed as part of an AR cycle, RFID readers (both heated and non-heated) read the
tags on the container and their identy and status is conrmed on-screen. If containers containing
samples of incompable origin come into contact at any stage of this process, the system acvates an
alarm and prompts the clinician to respond.
This manual is specically for the Embryology Heated Plate (and associated Tube Reader accessory) in
both its ush ed and sit on top conguraon.
Other devices in the RI Witness range have their own manuals, as does the soware.

Figure 4-1 Sit on Top Heated Reader Figure 4-2 Tube Reader Accessory

Secon 4

Product Overview

4

 
Temperature Sensor 5 x PT1000 (1 per Channel)
Temperature Control
Electrical heang is controlled by a built-in 5-channel PWM temperature
controller:
• Channel 1-4: Work surface surrounding the ITO glass window is
divided into quarters
• Channel 5: ITO glass window
Temperature controller accuracy: beer than ±0.2°C when calibrated
against a known reference.
Displayed resoluon: 0.1°C
Setpoint temperature range: 30-45°C
Displays 3 x 7-segment LED display shows the temperature reading from the
ITO glass window temperature sensor.
Connecvity USB plug type A
Power Supply
Input: 85-264VAC (100-240VAC Nominal), 47-63Hz,
<3A , Class I
Output: 48VDC, Max 4.6A (220W)
Operang Condions
Temperature: 15˚C (59˚F) to 40˚C (104˚F). Ambient temperature
must be > 5°C below setpoint.
Humidity: 15% to 85% RH (Non Condensing)
RFID Antennas
Embryology Heated Plate: 3 Antennas
Tube Reader Accessory: 2 Antennas
(5 Total)
RFID 50Ω Load at 13.56Mhz, 1W Max
Dimensions
Width: 460mm
Depth: 220mm
6-70-807 Thickness: 20mm
6-70-807-A/-B Thickness: 34mm
Mass 6-70-807: 3.0kg (plus Power Supply 1.0kg)
6-70-807-A/-B: 5.0kg (plus Power Supply 1.0kg)

Secon 5
RI Witness™ Basic Operaon
11

5


To turn the device on, plug the power cable from the device into the power supply in-line connector
ensuring it is fully inserted. Then plug the power supply into the wall power outlet.
Once the device is plugged in, it will display the current measured temperature on the display. The
status LED will remain o unl the temperature has stabilised at the specied setpoint. The me to
reach this will vary according to the ambient temperature, but will generally be within 15-30 minutes.
Once the temperature has stabilised, the green status light will illuminate (see “Alarms and System
Status” on page 18 for more informaon).
RI suggests that you keep the RI Witness computers and work areas (including the Embryology Heated
Plate) switched on. This means that the heang and monitoring is constant.

To shutdown the device remove all electrical power by disconnecng the cable from the electrical
outlet.

Plug the device into the tablet or PC (or aached USB hub) using the USB A cable that protrudes from
the device. Once the Windows operang system has recognised the devices within the Embryology
Heated Plate, open the RI Witness Work Area soware. To verify that the RI Witness Work Area soware
can communicate successfully, navigate to the Work Area Status window (click the yellow triangle or
press the icon). This will bring up the Work Area Status window where the ‘Embryology Reader’ and
‘Temperature Control’ should be listed in the Connected Devices secon with a green ck next to them.
For more detailed set up informaon, refer to the RI Witness soware manual (6-70-121UM).

The Embryology Heated Plate contains a built in user interface which allows access to basic temperature
setpoint and calibraon adjustment. A complete set of calibraon opons can only be accessed through
the RI Witness Work Area soware.
Setpoint
Adjustment
Indicator Light
Status
Indicator
Light
Oset
Adjustment
Indicator Light
Temperature Display
(shows ITO glass
window temperature)
Sengs
Buon
Down Buon
Up Buon
Figure 5-2 User Interface
Figure 5-1 Power Supply In-Line Connector

Secon 5
12
RI Witness™ Basic Operaon

5

The heated plate is divided into 5 areas for calibraon purposes. In order to achieve the correct sample
temperature place the sample on top of the heated areas shown below. Do not place samples on top
of the User Interface.
Figure 5-3 Embryology Heated Plate Heated Areas
Unheated Area
User Interface
Top Le
Heated Area
Top Right
Heated Area
Boom Le
Heated Area
Boom Right
Heated Area
When working with mulple samples on the heated plate, it is recommended that only one sample is
placed on the window heated area at a me.
Temperatures within the Petri dish are adjusted by changing the setpoint temperature as described on
the next page. The temperature inside a Petri dish will normally be slightly lower than the heated plate,
depending on ambient condions, type of Petri dish and the sample preparaon. Aer the system has
been installed in its operang locaon, the temperature of the heated plate should be adjusted to allow
for this dierence.
We recommend using a thermometer calibrated to 37°C ed with a small thermocouple probe, such
as the RI IVF Thermometer to measure the temperature inside the Petri dish.
Prepare a Petri dish that mimics your normal Petri dish preparaon and place it on the heated surface
in its normal posion. Place the probe of the thermometer in the centre of the dish against the boom
of the dish and allow the temperature reading to stabilise. Adjust the setpoint temperature unl the
desired temperature in the dish is reached, allowing 20 minutes (or as long as required) in between
each setpoint change to allow the Petri dish temperatures to stabilise.
Figure 5-4 Thermometer Probe Posioned in a Petri Dish
Window
Heated Area
Blue denotes
unheated area
Red denotes
heated area

Secon 5
RI Witness™ Basic Operaon
13

5
Funcons of the built-in user interface are shown below.

The temperature setpoint is applied to all heang channels and is set using the following procedure, or
from within the RI Witness Work Area soware. Refer to the RI Witness Soware Manual (6-70-121UM)
for further informaon.
1. Press and hold the Sengs buon for 3 seconds.
2. The Setpoint Adjustment Indicator light will ash. The Temperature Display will now show
the current setpoint (not the current temperature).
3. Adjust the value shown on the Temperature Display using the Up and Down buons
unl the desired setpoint is shown.
4. Save the temperature by pressing and holding the Sengs buon for 3 seconds.
A beep will be heard.
5. The Setpoint Adjustment Indicator light will go out and the Temperature Display will now
show the current temperature. Once the temperature has stabilised at the setpoint, the green
Status Indicator Light will illuminate.
 To exit the setpoint adjustment mode without saving changes, do not press any buons for a
short me and the device will return to normal operaon (the Setpoint Adjustment Indicator light will
go out).


To change the setpoint using the RI Witness WorkArea soware, click on the temperature displayed
at the boom right hand side of the screen. This will bring up a pop up box with up and down arrows
which can be used to adjust the setpoint temperature. The temperature controller will then begin
controlling using the new sengs .
Aer adjusng the setpoint temperature, check sample temperature inside the Petri dish.

Secon 5
14
RI Witness™ Basic Operaon

5

 It is only possible to calibrate the temperature of the ITO glass window using the built-in user
interface on the Embryology Heated Plate. To perform a full calibraon of all 5 heated areas, this must
be done from within the RI Witness Work Area soware.
Perform calibraon only if the displayed temperature is dierent to the actual surface temperature of
any of the 5 heated areas. The process of calibraon allows the user to manually adjust the temperature
so that the displayed temperatures match the temperature of the surface.
Before temperature calibraon can be performed the device must be in the same condions that it will
be in during normal operaon. The temperature calibraon is aected by ambient condions.
Place the probe of a calibrated thermometer in good thermal contact with the surface.
 Simply touching the probe on the surface is not adequate. Use a purpose-made surface probe and
use thermal transfer paste. Products sold for computer heatsinks are suitable, and RI can also supply
suitable materials. Wait at least 30 minutes to allow the temperature to stabilise before calibrang.
Heated areas are divided as shown below, with the ‘X’ denong recommended thermocouple posions
for calibraon:

During calibraon using the built-in user interface close the RI Witness Work Area soware to prevent
interference with the thermometer reading.
1. Posion the thermocouple probe on the Window in the locaon shown above.
2. Press and hold the Sengs and buons simultaneously for 3 seconds.
The Oset Adjustment Adjustment Indicator light will ash. The Temperature Display will
now show the current temperature (which may be a moving value).
3. Adjust the value shown on the Temperature Display using the Up and Down
buons unl the temperature matches that shown on the external thermometer.
4. Save the calibraon by pressing and holding the Sengs buon for 3 seconds. A beep will
be heard.
5. The Oset Adjustment Adjustment Indicator light will go out and the Temperature Display
will now show the current temperature with applied calibraon. Leave the probe in posion
Unheated Area
User Interface
Top Le Top Right
XX
X X
X
Boom Le
Window
Boom Right
Figure 5-5 Recommended Thermocouple Posions for Temperature Calibraon

Secon 5
RI Witness™ Basic Operaon
15

5
and once the temperature has stabilised at the setpoint, check that the calibraon is accurate.
Repeat the calibraon process if necessary. The green Status Indicator Light will illuminate once
temperatures have stabilised.
6. Aer adjusng calibraon check sample temperatures and adjust the setpoint temperature if
required.
 To exit the window calibraon mode without saving changes, do not press any buons
for a short me and the device will return to normal operaon. The Oset Adjustment Indicator
light will go out.

Full calibraon of the 5 heated areas requires that each of the areas is calibrated in turn.
1. Open the RI Witness Work Area soware and navigate to the WorkArea Status window.
2. Click on the yellow triangle or the  icon then click , then 
, then  then . The screen will now show the
current temperature and calibraon osets of the ve dierent heated areas.
 RF will be switched o automiacally when on the Temperature Control screen.
3. Each heated area is independent so the order of calibraon is not important. Posion the
thermocouple probe in one of the posions shown above.
4. Allow the reading to stabilise, then compare the temperature shown in the Work Area soware
with the thermometer reading.
5. A dierence within ± 0.2°C is acceptable. If the readings are outside this increase the oset to
increase the reading displayed by the soware, or decrease the oset to decrease the reading
displayed by the soware.
Allow a small delay for the oset change to register. When changing the oset, the temperature
controller will then begin controlling using the new sengs, so the surface temperature of that heated
area may take a short me to re-stabilise.
6. Repeat this process for all 5 heated areas.
7. Once calibraon is complete it is advisable to verify the temperature of each heated area to
check that temperature calibraon has been carried out eecvely. Aer adjusng calibraon,
check sample temperatures and adjust the setpoint temperature if required.

Secon 5
16
RI Witness™ Basic Operaon

5

The Tube Reader Antenna is an accessory for the Embryology Heated Plate that allows tags to be read in
a vercal orientaon. It is specically designed to read tags placed on tubes in the RI Tube Holder. The
Tube Reader Antenna is a passive device that only becomes powered when aached to the Embryology
Heated Plate. The correct mounng orientaon posion is shown below in Figure 5-6.
Refer to “Secon 7- Care and Maintenance” on page 23 for cleaning precauons relang to the Tube
Reader Antenna.
Figure 5-6 Tube Reader Connecons on the Embryology Heated Plate
Figure 5-7 Tube Reader Correctly Mounted on the Embryology Heated Plate
Tube Reader
Antenna
Tube Reader Antenna
Connecons

Secon 6
Troubleshoong


6

  
Tags Reading
Intermiently or Only
in Certain Areas
Loose connecon Check security of USB and power cable
connecons.
Antenna not tuned
properly
Navigate to the  screen, then
click  , then 
, then , then .
RF Noise/interference Other devices in the lab can cause RF noise/
interference, contact an RI service representave.
Faulty Device Contact an RI Service representave.
Tags Not Reading
Broken tag Check the tag on another device.
Poor/no connecon or
no power.
Check security of USB and power cable
connecons. Verify that the light on the power
supply is illuminated.
Tag not encrypted
Navigate to the  screen, then
click  , then 
 then click the down arrow next to Tags.
Non encrypted tags are shown as .
WorkArea conguraon
Navigate to the   screen, then
click  , then ,
then  , to check that the number of
antennas (channels) is 5 for the Embryology Reader
with the Tube Reader Antenna Accessory.
Antenna not tuned
Navigate to the  screen, then
click  , then 
, then , then .
Faulty Device Contact RI or an RI Service Representave.