Bio-Tek BioStack 4 User manual

Operator’s Manual
BioStack™
Microplate Stacker

BioStack™ Microplate Stacker
Operator's Manual
© 2018
BioTek Instruments, Inc.
PN 7311000 Rev AH

ii | BioStack Operator's Manual
Notices
BioTek® Instruments, Inc.
Highland Park, PO Box 998
Winooski, VT USA 05404-0998
© 2018, BioTek Instruments, Incorporated. No part of this publication may be
reproduced, transcribed, or transmitted in any form or by any means electronic or
mechanical, including photocopying and recording, for any purpose other than the
purchaser's use without the written permission of BioTek Instruments, Inc.
Trademarks
BioTek® is a registered trademark, and BioStack™, 405™ Microplate Washer,
EL406™, ELx405™, Eon™, Epoch™, Gen5™, Liquid Handling Control™,
MicroFill™, MultiFlo™, MultiFlo™ FX, PowerWave™, Precision™, Precision
Power™, Cytation™ and Synergy™ are trademarks of BioTek Instruments, Inc.
Microsoft® and Windows® are registered trademarks of Microsoft Corporation in
the United States and/or other countries.
All other trademarks are the property of their respective holders.
Restrictions and Liabilities
Information in this document is subject to change and does not represent a
commitment by BioTek Instruments, Inc. Changes made to the information in this
document will be incorporated in new editions of the publication. No
responsibility is assumed by BioTek for the use or reliability of software or
equipment that is not supplied by BioTek or its affiliated dealers.
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Notices| iii
Contents
Notices ii
Contact Information vi
Global Service and Support vi
Customer Service and Sales vi
Service/Technical Assistance Center (TAC) vi
European Coordination Center/Authorized European Representative vi
Revision History vii
Document Conventions xi
Intended Use Statement xi
Quality Control xii
Warranty and Product Registration xii
Warnings xii
Hazards xiii
Precautions xiv
CE Mark xvi
Directive 2014/30/EU: Electromagnetic Compatibility xvi
Directive 2014/35/EU Low Voltage (Safety) xvi
Directive 2012/19/EU: Waste Electrical and Electronic Equipment xvii
Directive 98/79/EC: In Vitro Diagnostics (if labeled for this use) xvii
Electromagnetic Interference and Susceptibility xvii
USA FCC CLASS A xvii
Canadian Department of Communications Class A xvii
User Safety xviii
Safety Symbols xix
BioStack 3 and BioStack 4: Secure Gripper Before Moving xx
Introduction 1
Introducing the BioStack 2
Product Description 3
BioStack 4: Notes about Handling Lidded Plates 4
Package Contents 6
Optional Accessories 6
Specifications 9
Stay-On Lid Mode (BioStack 4 Only) 10
Installation 13
Upgrade Scenarios 14
Unpack and Inspect the Instrument 15
Setting Up the BioStack 17
Remove the Shipping Hardware—BIOSTACK2WR 18
Remove the Shipping Hardware—BioStack 3 20
Remove the Shipping Hardware—BioStack 4 23
Wrist Angle Setting Requirements 26
0 Degree Orientation for Liquid Handlers 27
Dip Switch Settings 28
Change Setting for Wrist Angle 29
Change Setting for 50-Plate Stacks 30
BioTek Instruments, Inc.

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Test Plates for Compatibility—BioStack 4 Only 30
Connect to Power 31
Connect to Computer 32
Connect to Liquid Handler 33
Where to Go Next 35
Repacking the BioStack 36
Install the Shipping Hardware—BioStack2WR 37
Install the Shipping Hardware—BioStack 3 37
Install the Shipping Hardware—BioStack 4 38
Repacking—Install Shipping Panel 39
Operation 41
Before You Start 42
Load Plates into Input Stack 43
Load Plates Using the Pedestal 44
Supported Microplate Types and Dimensions 45
Processing Microplates 46
Controlling the BioStack: 46
Stopping Plate Processing 47
Restack the Plates 49
Processing Plates with Lids 49
Plate De-Lidding: How It Works 50
Prevent Condensation on Plate Lids 51
Plate Lid Definition Files 52
Microplate and Lid Dimensions 53
Plate Lid Advanced Dimensions 54
Start Up the BioStack 57
Maintenance 59
Overview 60
Recommended Maintenance Schedule 60
Warnings and Precautions 61
Required Materials 61
Routine Cleaning Procedure 63
Decontamination 64
Tools and Supplies 65
Decontaminate the BioStack 65
Cleaning and Lubricating the Linear Ways 66
Qualification 69
Overview 70
Recommended Qualification Schedule 70
Installation Qualification 72
Operational Qualification Procedure 72
Troubleshooting & Error Codes 73
Troubleshooting 74
Communication Error Codes 74
BioStack Instrument Errors 76
Plate Lid Definition Errors 82
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Notices| v
Washer or Dispenser Communication Error Codes 85
BioStack Sensor Numbers 86
BioStack Motor Numbers 87
Interfacing Instrument Numbers 87
Plate Stacked Height 88
Change Setting for Low-Profile Plates 89
Loosen Plate Carrier Set Screws - BioStack 4 Only 90
Adjust the Stack Dogs 91
Install the Barcode Scanner 93
Barcode Scanner Overview 94
Install the Barcode Scanner 94
Change Dip Switch Setting for Barcode Scanner 97
Install the Scanner Cable Duct 97
Preparing and Attaching Barcode Labels 99
Scanner Test with Readers 101
To Report Barcodes with Reader Results 101
Scanner Test with Precision/XS 103
To Report Scanned Codes with Precision/XS 104
BioTek Instruments, Inc.

vi | BioStack Operator's Manual
Contact Information
BioTek Instruments, Inc.
Highland Park, P.O. Box 998
Winooski, Vermont 05404-0998 USA
Global Service and Support
BioTek instrument service and repair is available worldwide at several of BioTek’s
International Service Centers and in the field at your location. To arrange for service
or repair, contact the office nearest you; visit www.biotek.com for up-to-date
contact information. For customer service, sales, and technical assistance, refer to
the information below.
Customer Service and Sales
Internet: www.biotek.com
Phone: [phone] (toll-free in the US)
 802-655-4740(outsidetheUS)
Fax: [phone]
Email: [e-mail]
Service/Technical Assistance Center (TAC)
Phone: [phone] (toll-free in the US)
 802-655-4740(outsidetheUS)
Fax: [phone]
Email: [e-mail]
European Coordination Center/Authorized European Representative
BioTek Instruments GmbH
Kocherwaldstrasse 34
D-74177 Bad Friedrichshall
Germany
Internet: www.biotek.de
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Revision History| vii
Phone: [phone]
Fax: +49(0)7136968111
Email: [e-mail]
Revision History
Rev Date Changes
A 11/2002 First issue.
B 5/2003 Throughout: Clarified the compatibility of the ELx405 with the BioStack by
specifying the Washer’s Auto Plate and Select models only. Updated
contact information, Safety Symbols, and Warranty.
C 10/2003 Preface: Updated the Intended Use statement to distinguish between the
European Union and all other jurisdictions.
D 06/2004 Throughout: Reformatted manual for cosmetic effect. Added references
about compatibility of the BioStack with the ELx405 HT and ELx405 Select
CW Microplate Washers. Added new sections about compatibility,
installation, operation, alignment, etc., of the Precision and Precision XS.
Revised the Technical Support section and added new sections on Depot
Service Contracts and Applications Support. Enhanced Introduction,
Installation, Operation, and Maintenance chapters.
E 06/2005 Throughout: Added information on the new barcode scanner and USB port.
Changed ELx405 “Auto” model to “ELx405.”
Moved instructions from former Appendix B, Serial Cable Connections and
Appendix C, Mounting the Aligning Plates and Posts into Chapter 3,
Installation.
Chapter 5: Simplified/clarified IQ and OQ sections. Chapter 7: Added KC4
error codes for BioStack operation with readers, and BioStack barcode
scanner error codes.
F 05/2006 Added instructions for using Gen5 software. Preface: Updated safety
information and removed Warranty, Registration Card, and Registration
Online sections in Preface. Added laser beam warning. Appendix B: Added
laser beam warning.
G 07/2006 Added instructions for installing/operating the BioStack with the Synergy 2.
H 12/2006 Added instructions for installing and operating the BioStack with the
NanoQuot. In Chapter 5 and Appendix B: Added the Barcode Scanner Test
as an optional IQ and OQ test.
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viii | BioStack Operator's Manual
Rev Date Changes
I 06/2007 Added instructions for installing and operating the BioStack with the
Synergy 4. Updated error code information. Incorporated manual update
revision H1 as Appendix C, Reconfiguration of the BioStack. Added
Appendix D, Required Software Versions.
J 08/2007 Added references to the Liquid Handling Control (LHC) Software throughout
the manual, and instructions for installation/operation of the software for
PC control of the BioStack and ELx405.
K 10/2007 Added instructions for installing and operating the BioStack with the
MicroFlo Select.
L 03/2008 Added instructions for installing and operating the BioStack with the
PowerWave XS2. Changed “μFill” to “MicroFill.”
M 06/2008 Changed “Bio-Stack” to “BioStack.” Added references to the fixed wrist
model (PN BIOSTACK2) and rotational wrist model (PN BIOSTACK2WR).
Added instructions for installation/operation of the new models with
interfacing instruments.
N 10/2008 Added instructions for installing and operating the BioStack with the EL406.
Changed “Alignment Kit” to “Integration Kit” throughout. Added more
information about installation of two BioStacks with two interfacing
instruments (ELx405, MicroFlo Select, EL406).
O 12/2008 Added instructions for installing and operating the BioStack with the
Synergy Mx. Removed references to obsolete BioStack PN BIOSTACK.
P 04/2009 Added information regarding instrument control of the EL406 and
installation/operation instructions for controlling the BioStack and EL406
via the keypad. Added more information about how the BioStack barcode
scanner works in Appendix B. Added instructions or notes throughout the
manual instructing the user to turn the BioStack on before the interfacing
instrument, and to manually raise the BioStack’s claw/gripper above the
interfacing instrument’s plate carrier or supply station (Precision) before
turning the BioStack on.
Q 01/2010 Added instructions for installing and operating the BioStack with the
Synergy H4 reader.
R 09/2010 Overall: Streamlined and rearchitected content to enhance usability and
support maintenance and reuse. Moved installation and operation
instructions, software version compatibility tables, software data sheets,
and information on obtaining software version information out of the main
Operator’s Manual and into individual, instrument-specific PDF files on the
BioStack Operator’s Manual CD. Added support for the MultiFlo Dispenser.
Preface: Updated Intended Use Statement; Warnings, Hazards, and
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Revision History| ix
Rev Date Changes
Precautions; Directives; and Safety Symbols.
Chapter 1 Introduction: Updated Package Contents and Optional
Accessories lists. Chapter 2 Installation: Added “Configure for 50-Plate
Stacks.” Chapter 5 Instrument Qualification: Removed IQ Checklists.
Moved the Software Data Sheets to the individual instrument-specific PDF
files. Chapter 6 Error Codes: Removed error code tables for MicroFlo and
EL406 Interface Software, and Gen5/KC4 Function Call Errors.
S 11/2010 Added instructions for installing and operating the BioStack with the
Synergy H1 reader. Emphasized the importance of orienting microplates in
the input stack to match the expected placement of well A1 on the
interfacing instrument’s plate carrier.
T 8/2011 Added instructions for installing/operating the BioStack with the Eon,
Epoch.
U 3/2012 Added instructions for installing and operating the BioStack with the 405
TS. Added references to the 10-plate stacks.
V 6/2012 Added support for BIOSTACK3WR (for liquid handlers). Removed
references to BioStack2. Added ‘Service’ and ‘Accessories’ hazard
warnings. Added ‘Spare Parts’ precaution. Changed all references from
claw/gripper to gripper. Added Wrist Angle Setting Requirement and Dip
switch Settings content. Revised descriptions of the microplate
requirements. Replaced former Appendix B, Microplate Stack
Adjustment/Configuration for Half-Height Plates with section in
Troubleshooting chapter: Adjust Stack Dogs. Updated error codes and
added Troubleshooting guidelines to the same chapter. Omitted former
Appendix C, Information for External Developers, as it was obsolete.
Updated format and text styles, replaced some drawings with photos.
Revised the liquid handler instrument-specific sections; conversely, the
reader instrument-specific PDFs are unchanged since the last revision. The
Nanoquot instrument-specific section has been omitted.
W 7/2012 Added support for BioStack3 for readers and for controlling both BioStack
models using Gen5 alone (i.e. BioStack PC Control Software is no longer
needed for the readers). Consolidated the Integration Kits when applicable,
i.e. universal aligning base plates support both BioStack models. Removed
references to obsolete aligning base plate in instrument-specific
instructions. Added units to the barcode label graphic.
X 4/2013 Added instructions for installing and operating the BioStack with the
Cytation 3. Corrected or improved content based on suggestions from field
staff, including deleting the statement that barcode labels can be purchased
from BioTek. Added references to the rubber band that secures the
BioStack3's wrist during shipping. Recommended using rubber bands to
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Rev Date Changes
secure gripper before moving the BioStack 3.
Y 11/2013 Added instructions for installing and operating the BioStack with the
MultiFlo FX. Added Precision Universal models (PRC384U) to the list of
instruments that are not BioStack-compatible. Restored references to, and
added a diagram for 0° integration for liquid handlers and the
BIOSTACK2WR. Added "Space Requirement Dimensions" for most
interfacing instruments.
Z 12/2013 Introduced BioStack 4 and its support of plate lids during processing. Added
hazard label and description: cutting fingers/hand. Added "Plate
Compatibility Test" for BioStack4 only. Added support for the Synergy Neo
- BioStack4 integration.
AA 6/2014 Added support for new instruments: Epoch2 and Synergy HTX. Added a
warning that the PowerWave HT is not compatible with the BioStack 4 and a
"strong recommendation" to measure the plate and lid type before use to
verify they meet the minimum requirements for de-lidding operations with
the BioStack 4.
AB 9/2014 Updated specifications to include certain low-density plates with lids that
are supported in "stay-on lid" mode. Added references to stay-on lid mode
where applicable. Corrected the space requirement for liquid handlers:
increased the depth required by six inches to account for wrist movement.
AC 12/2014 Added support for Cytation 5. Updated the "Stay-on Lid" mode description
to describe the newly relabeled stacks required to support this feature, i.e.,
Tall Lidded Plate Stacks. Updated notice of compliance with EU Directives.
AD 2/2015 Updated Synergy Neo integration instructions to match new and improved
alignment hardware. Added new 28 volt power supply to parts list.
AE 3/2015 Reverted contents to match revision AC.
AF 7/2015 Added support for Synergy Neo2, updated Contact Information, changed
RMA to Service Call Notice (SCN) number, updated Synergy Neo and
Synergy Neo2 integration kit to PN 7310055
AG 2017 Updated PN for replacement shipping materials 7313002 to 1163003;
removed reference to the ANSI standard in the microplate specification sec-
tion; add note to “Install and Run BioStack with the Synergy H1” to point
out position of bracket on alignment plate, which varies depending on
which BioStack is used; added Cytation 1 support; resolved EPR 24692 by
adding error code 2002 to the list; modified instructions for installing soft-
ware and testing communication in the Install and Operate the BioStack
with Precision document; added USB and serial cable part numbers to the
fluid interfacing instrument documents.
BioStack™ Microplate Stacker

Document Conventions| xi
Rev Date Changes
AH 12/2018 Updated Epoch 2 information to correspond with the updated Epoch 2 instru-
ment; corrected alignment plate PN for Synergy H1; updated the drawing
of the Cytation showing the space needed for an instrument with a Cooling
Accessory installed; updated PN for BioStack2 shipping container to PN
7310014; updated BioStack leg PN for use with Epoch 2 to 7310570;
updated the PN for the baseplate for the Microflo FX to 7312138; added
error code 020D.
Document Conventions
This manual uses the following typographic conventions:
nThis note format calls attention to important information.
Warnings are presented in this style to call attention to potential hazards and
other safety concerns.

This icon calls attention to important safety information.
Tips and suggestions for improving performance are formatted this way.
Intended Use Statement
The BioStack Microplate Stacker is an automated microplate stacking system that is
designed to systematically transfer a stack of microplates to and from compatible
BioTek laboratory instruments wherever washing, dispensing, pipetting, or reading
of multiple microplates is performed.
If the instrument has an “IVD” label it may be used for clinical and non-clinical
purposes, including research & development. If there is no such label the
instrument may only be used for research & development or other non-clinical
purposes.
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xii | BioStack Operator's Manual
Quality Control
It is considered good laboratory practice to run laboratory samples according to
instructions and specific recommendations included in the assay package insert for
the test to be conducted. Failure to conduct Quality Control checks could result in
erroneous test data.
Warranty and Product Registration
Please take a moment to review the Warranty information that shipped with your
product. Please also register your product with BioTek to ensure that you receive
important information and updates about the product(s) you have purchased.
You can register online through BioTek’s Customer Resource Center (CRC) at
www.biotek.com or by calling 888/451-5171 or 802/655-4740.
Warnings
Operate the instrument on a level, stable surface away from excessive
humidity.
When operated in a safe environment, according to the instructions in this
manual, there are no known hazards associated with the BioStack. However,
the operator should be aware of certain situations that could result in serious
injury: see Hazards and Precautions.
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Hazards| xiii
Hazards
The following hazard warnings are provided to help avoid injury:
Warning! Power Rating. The instrument’s power supply or power cord must
be connected to a power receptacle that provides voltage and current within the
specified rating for the system. Use of an incompatible power receptacle may
produce electrical shock and fire hazards.
Warning! Electrical Grounding. Never use a plug adapter to connect primary
power to the external power supply. Use of an adapter disconnects the utility
ground, creating a severe shock hazard. Always connect the power cord directly to
an appropriate receptacle with a functional ground.
Warning! Service. Only qualified technical personnel should perform service
procedures on internal components.
Warning! Accessories. Only accessories which meet the manufacturer’s
specifications shall be used with the instrument.
Warning! Liquids. Avoid spilling liquids on the instrument; fluid seepage into
internal components creates a potential for shock hazard or instrument damage. If a
spill occurs while a program is running, abort the program and turn the instrument
off. Wipe up all spills immediately. Do not operate the instrument if internal
components have been exposed to fluid.
Warning! Unspecified Use. Failure to operate this equipment according to the
guidelines and safeguards specified in this manual could result in a hazardous
condition.
Warning! Software Quality Control. The operator must follow the
manufacturer’s assay package insert when modifying software parameters and
establishing reading, washing, or dispensing methods. Failure to conduct quality
control checks could result in erroneous test data.
Warning! Internal Voltage. Always turn off the power switch and unplug the
power supply before cleaning the outer surface of the instrument.
Warning! Potential Biohazards. Some assays or specimens may pose a
biohazard. Adequate safety precautions should be taken as outlined in the assay’s
package insert. This hazard is noted by the symbol shown here. Always wear safety
glasses and appropriate protective equipment, such as chemically resistant rubber
gloves and apron.
Warning! Laser Beam. Serious eye injury may occur if you stare directly into
the laser beam of the barcode scanner during operation of the scanner. This hazard
is noted by the symbol shown here. Do not look directly into the laser beam during
operation of the scanner.

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xiv | BioStack Operator's Manual
Warning! Pinch Hazard. Some areas of the instrument or its components can
present pinch hazards when the instrument is operating. These areas are marked
with the symbol shown here. Keep hands/fingers clear of these areas when the
instrument is operating.
Warning! Cutting of Fingers or Hand Hazard. The metal plate gripper
presents a cutting hazard to fingers/hands when the instrument is operating. The
gripper is marked with the symbol shown here. Keep fingers/hands away from the
gripper when the instrument is operating.
Precautions
The following precautions are provided to help avoid damage to the instrument(s):
Caution: Service. The instrument should be serviced by BioTek-authorized
service personnel. Only qualified technical personnel should perform troubleshooting
and service procedures on internal components.
Caution: Spare Parts. Only approved spare parts should be used for
maintenance. The use of unapproved spare parts and accessories may result in a
loss of warranty and potentially impair instrument performance or cause damage to
the instrument.
Caution: Environmental Conditions. Do not expose the instrument to
temperature extremes. For proper operation, temperaturess near the instrument
should remain within the range listed in the Specifications section. Performance
may be adversely affected if temperatures fluctuate above or below this range.
Caution: Sodium Hypochlorite. Do not expose any part of the instrument to
the recommended diluted sodium hypochlorite solution (bleach) for more than 20
minutes. Prolonged contact may damage the instrument surfaces. Be certain to
rinse and thoroughly wipe all surfaces.
Caution: Power Supply. Only use the power supply shipped with the
instrument. Operate this power supply within the range of line voltages listed on it.
Caution: Disposal. Dispose of the instrument according to Directive
2002/96/EC, “on waste electrical and electronic equipment (WEEE),” or local
ordinances.
Caution: Warranty. Failure to follow preventive maintenance protocols may
void the warranty.
Caution: Shipping Hardware. All shipping hardware (e.g., shipping panel,
shipping block, carrier shipping screws, etc.) must be removed before operating the
instrument and reinstalled before repackaging the instrument for shipment.
Caution: Waste Sensor Port (for customers who have purchased the
BioStack for use with the ELx405, 405 TS/LS, or EL406). The waste sensor port on
the back of the washer/dispenser is the same type as the 24-VDC power connector
on the back of the BioStack. Do not plug the BioStack’s external power supply into
BioStack™ Microplate Stacker

Precautions| xv
the washer’s/dispenser’s port; it will permanently damage internal components.
Caution: Aligning Posts. When installing the BioStack’s four aligning posts,
use caution not to cross thread these parts. Finger-tighten only!
Caution: BioStack Barcode Scanner Mirror. Do not scratch or damage
the mirror when unpacking or installing the barcode scanner.
Caution: Electromagnetic Environment. Per IEC 61326-2-6 it is the user’s
responsibility to ensure that a compatible electromagnetic environment for this
instrument is provided and maintained in order that the device will perform as
intended.
Caution: Electromagnetic Compatibility. Do not use this device in close
proximity to sources of strong electromagnetic radiation (e.g., unshielded
intentional RF sources), because these may interfere with the proper operation.
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xvi | BioStack Operator's Manual
CE Mark
Based on the testing described below and information contained
herein, this instrument bears the CE mark.
nNote: Refer to the Declaration of Conformity for specific details.
Directive 2014/30/EU: Electromagnetic Compatibility
Emissions—Class A
The system has been type-tested by an independent, accredited testing
laboratory and found to meet the requirements of EN 61326-1: Class A for
Radiated Emissions and Line Conducted Emissions.
Verification of compliance was conducted to the limits and methods of EN 55011
(CISPR 11) Class A. In a domestic environment it may cause radio interference,
in which case, you may need to take measures to mitigate the interference.
Immunity
The system has been type-tested by an independent, accredited testing
laboratory and found to meet the requirements of EN 61326-1 and EN 61326-2-6
for Immunity. Verification of compliance was conducted to the limits and
methods of the following:
EN 61000-4-2, Electrostatic Discharge
EN 61000-4-3, Radiated EM Fields
EN 61000-4-4, Electrical Fast Transient/Burst
EN 61000-4-5, Surge Immunity
EN 61000-4-6, Conducted Disturbances from RFI
EN 61000-4-11, Voltage Dips, Short Interruptions and Variations
Directive 2014/35/EU Low Voltage (Safety)
The system has been type-tested by an independent testing laboratory and was
found to meet the requirements of this Directive. Verification of compliance was
conducted to the limits and methods of the following:
EN 61010-1, “Safety requirement for electrical equipment for measurement,
control and laboratory use. Part 1, General requirements.”
EN 61010-2-081, “Particular requirements for automatic and semi-automatic
laboratory equipment for analysis and other purposes.”
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Electromagnetic Interference and Susceptibility| xvii
Directive 2012/19/EU: Waste Electrical and Electronic Equipment
Disposal Notice: Dispose of the instrument according to Directive 2012/19/EU,
“on waste electrical and electronic equipment (WEEE)” or local ordinances.
Directive 98/79/EC: In Vitro Diagnostics (if labeled for this use)
nProduct registration with competent authorities
nTraceability to the U.S. National Institute of Standards and Technology (NIST).
EN 61010-2-101 Particular requirements for in vitro diagnostic (IVD) medical
equipment.
Electromagnetic Interference and Susceptibility
USA FCC CLASS A
RADIO AND TELEVISION INTERFERENCE
NOTE: This equipment has been tested and found to comply with the limits
for a Class A digital device, pursuant to Part 15 of the FCC Rules. These limits
are designed to provide reasonable protection 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 instruction manual, may cause harmful
interference to radio communications. Operation of this equipment in a
residential area is likely to cause harmful interference, in which case the user
will be required to correct the interference at their own expense.
In order to maintain compliance with FCC regulations shielded cables must be
used with this equipment. Operation with non-approved equipment or
unshielded cables is likely to result in interference to radio and television
reception.
Canadian Department of Communications Class A
This digital apparatus does not exceed Class A limits for radio emissions from
digital apparatus set out in the Radio Interference Regulations of the Canadian
Department of Communications.
Le present appareil numerique n'émet pas de bruits radioelectriques depassant
les limites applicables aux appareils numerique de la Class A prescrites dans
le Reglement sur le brouillage radioelectrique edicte par le ministere des
Communications du Canada.
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xviii | BioStack Operator's Manual
User Safety
This device has been type-tested by an independent laboratory and found to meet
the requirements of the following:
lUnderwriters Laboratories UL 61010-1 “Safety requirements for electrical
equipment for measurement, control and laboratory use; Part 1: general
requirements.”
lCanadian Standards Association CAN/CSA C22.2 No. 61010-1 “Safety
requirements for electrical equipment for measurement, control and
laboratory use; Part 1: general requirements.”
lEN 61010 Standards. See CE Mark on page xvi.
BioStack™ Microplate Stacker