Technimount System PRO 77 Series User manual

BRACKET PRO SERIE®77
USER GUIDE

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2 BP77 UG 202108-01 www.technimount.com
Copyright 2021 Technimount E.M.S. Holding Inc. (Technimount), an aliated company of Technologies CGC Inc. All
Rights Reserved. No part of this publicaon may be reproduced, transmied, transcribed, stored in a retrieval system,
or translated into any language in any form or by any means without the wrien permission of Technimount or its
aliate companies.
Trademark Aribuons:
Bracket Pro Serie®, Technimount EMS™ are registered trademarks of Technologies CGC Inc.
Laerdal Compact Sucon Unit® 4 (LCSU® 4) is a registered trademark of Laerdal.
Technimount does not have a commercial relaonship with Laerdal. Laerdal does not promote or sell Technimount
products.
In order to ensure connuous improvements to our products and services, we invite you to communicate your
comments to our Customer Service Department at customerser[email protected].
LEGAL NOTICE
Technologies CGC Inc. or Technimount E.M.S. Holding Inc. or its aliates are not expressly associated with the
markeng, distribuon or sale of Laerdal products.
The purchase and use of products designed by Technimount are subject to this limitaon of liability. It is important to
understand that, as Technimount is not the manufacturer of the Stryker (or other brand) stretcher or the manufacturer
of the medical equipment (Dräger or other brand), Technimount cannot guarantee the resistance and durability of
such stretchers and other equipment installed on it.
COPYRIGHT

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OFFICE ADDRESS
Technimount E.M.S. Holding Inc.
3770 Jean Marchand Street, Suite 100-C
Quebec (QC) G2C 1Y6
Canada
[email protected]
www.technimount.com
T + 1 888.639.2758
F + 1 855.339.6351
NOTE:
For any issues with your Technimount product, its components, or for any technical quesons during the installaon
or maintenance processes, please send an email to [e-mail].
Please have the serial number of your Technimount product available (as shown in the gure below) when calling
Technimount Technical Support. Include the serial number in all wrien communicaons.
SERIAL NUMBER LOCATION
CONTACT INFORMATION
The serial
number is
written under
the bracket
as shown in
this image

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TABLE OF CONTENTS
COPYRIGHT ............................................................................................................................................................2
Legal Notice ...................................................................................................................................................................2
CONTACT INFORMATION.......................................................................................................................................3
Symbols and Definitions ...............................................................................................................................................6
Warning/Caution/Note ................................................................................................................................................7
Product Illustration .....................................................................................................................................................8
Bracket Pro Serie 77 ..............................................................................................................................................8
Front View ..........................................................................................................................................................................8
Back View ............................................................................................................................................................................9
INTRODUCTION ................................................................................................................................................... 10
Purpose of the Document ..........................................................................................................................................10
Product Description ...................................................................................................................................................10
Intended Use of the Product .....................................................................................................................................10
Limitation of Liability ..................................................................................................................................................10
Technical Specifications..............................................................................................................................................11
SUMMARY OF SAFETY PRECAUTIONS ................................................................................................................ 12
Warning/Caution/Note ..............................................................................................................................................12
NOTICE/CERTIFICATION ...................................................................................................................................... 14
INSTALLATION GUIDE .......................................................................................................................................... 15
Removing the Packaging for Installation .................................................................................................................15
Tools Required for Installation.................................................................................................................................15
Identification of Components ....................................................................................................................................16
Bottom Support Block .........................................................................................................................................16
Hardware Kit ........................................................................................................................................................16
Installation of the Bracket onto the Laerdal Compact Suction Unit 4 .................................................................17
Installation of the Canister into the Bracket .........................................................................................................19
Removing the Canister from the Bracket .................................................................................................................20
MAINTENANCE GUIDE......................................................................................................................................... 21
Cleaning .......................................................................................................................................................................21
Cleaning Process ..................................................................................................................................................21
Removal of Iodine Compounds ...........................................................................................................................22
Preventive Maintenance .............................................................................................................................................22
Inspection Process and Schedule...............................................................................................................................23
Maintenance Program .........................................................................................................................................23
Inspection and Maintenance Record .........................................................................................................................24
Training Record ...........................................................................................................................................................25
Replacement Parts .......................................................................................................................................................26
WARRANTY .......................................................................................................................................................... 27
Warranty Policy ..........................................................................................................................................................27
Limited Responsibility and Warranty .........................................................................................................................27
International Warranty Clause .................................................................................................................................27

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TABLE OF CONTENTS
RETURN POLICY ................................................................................................................................................... 28
Return Policy ...............................................................................................................................................................28
Prior to 30 Days ...................................................................................................................................................28
Prior 45 Days ........................................................................................................................................................28
Prior 60 Days ........................................................................................................................................................28
Return Authorization .................................................................................................................................................28
Damaged Merchandise ................................................................................................................................................29
Claim Process ..............................................................................................................................................................29
Required Information ..........................................................................................................................................29
Findings and Conclusion .....................................................................................................................................29
Questions about our Policy .......................................................................................................................................29

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INTRODUCTION
SYMBOLS AND DEFINITIONS
SYMBOL DESCRIPTION
Warning and Cauon, special aenon is required. Consult
accompanying documents
Safe working load symbol and Load balance symbol

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WARNING/CAUTION/NOTE
The word warning, cauon, or note carry special meaning and should be carefully reviewed.
SYMBOL DESCRIPTION
Warning
Alerts the reader about a situaon which, if not avoided, could
result in death or serious injury. It may also describe potenal
serious adverse reacons and safety hazards.
Caution
Alerts the reader of a potenally hazardous situaon, which, if
not avoided, may result in minor or moderate injury to the user
or paent or damage to the equipment or other property. This
includes special care necessary for the safe and eecve use of the
device to avoid damage that may occur as a result of use or misuse.
NOTE Provides special informaon about the product.
INTRODUCTION

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PRODUCT ILLUSTRATION
BRACKET PRO SERIE 77
Front View
INTRODUCTION
Strap to Secure
800ml Canister
Bracket for
800ml Canister
High-Density Aluminum with
Black-Anodized Finish

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PRODUCT ILLUSTRATION (CONTINUED)
BRACKET PRO SERIE 77 (SUITE)
Back View
INTRODUCTION
Boom Support Block to
Secure Medical Device
An-Rotaon Micro Disc for
Installaon on Vercal and
Wall Mounng Systems

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INTRODUCTION
PURPOSE OF THE DOCUMENT
This user guide is designed to assist you with the installaon, operaon and maintenance of the Technimount Bracket
Pro Serie 77 for the Laerdal Compact Sucon Unit 4 (LCSU 4).
PRODUCT DESCRIPTION
The Bracket Pro Serie 77 is a unique soluon to mount the Laerdal Compact Sucon Unit 4 in dierent applicaons
such as, on surface, a vercal system, stretcher or wall systems. It is designed to securely support and transport the
Laerdal Compact Sucon Unit 4 in pre-hospital and hospital environments. The Bracket Pro Serie 77 provides a higher
exibility for dierent EMS/CCT protocols and applicaons. It is recommended for the safe transport of the Laerdal
Compact Sucon Unit 4 during inter-hospital transfers for neonatal crical care.
INTENDED USE OF THE PRODUCT
The Bracket Pro Serie 77 is a mounng soluon to securely transport the Laerdal Compact Sucon Unit 4 during inter-
hospital transfers. It is designed to be installed on the equipment as described in this user guide. The Bracket Pro Serie
77 is for crew who has received the appropriate training necessary to operate the equipment in the eld according to
its intended use as outlined in this user guide. Please read this user guide thoroughly before using this equipment. To
ensure the safe operaon of this equipment, it is highly recommended to train sta prior to use.
LIMITATION OF LIABILITY
Technimount has designed a system to aach and install medical equipment owned by the customer on an incubator
transport stretcher manufactured by Stryker and involving or not a Dräger or other incubator brand.
The purchase and use of products designed by Technimount are subject to this limitaon of liability clause. It is
important to understand that, as Technimount is not the manufacturer of the Stryker stretcher (or other brand)
nor the manufacturer of the incubators (Dräger or other brand), Technimount cannot guarantee the resistance and
durability of such stretchers and other equipment installed on it.
In addion, the mounng systems are designed by Technimount to install dierent medical equipment. Therefore,
Technimount is not responsible for any damage that may result from the installaon of mulple medical equipment
on the stretcher. For example, risks related, but not limited to, potenal stretcher overloading, pping, interference
between equipment, access restricon or other.
The Neonatal Stretcher System was developed by Technimount to meet an important market need, however, this
transport system involves risks that remain under the sole responsibility of the customer. It is important to instruct
your sta and partners to use Technimount products according to the safest pracces and in accordance with the
user's guide we provide. In addion, follow the safety guidance from the users guides from the manufacturers of
the medical devices, incubators and transport stretcher system. Technimount will not be held responsible for any
misuse of the product. Therefore, by conrming the purchase and accepng delivery of the transport system or any
Technimount product, this constutes conrmaon of consent to this limitaon of liability clause.

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INTRODUCTION
TECHNICAL SPECIFICATIONS
Product Name Bracket Pro Serie® 77
Product Descripon Bracket for Transport of LCSU® 4 on Stretcher during Neonatal Crical Care
Compability of Medical Device* Laerdal Compact Sucon Unit® 4
Environment of Usage EMS/CCT (Ground) - Hospital/Clinic
Product Secon Material • Main Assembly: Aluminum 6061-T6
• An-Rotaon Micro Disc: Aluminum 6061-T6
Product Finish • Main Assembly: Black-Anodized Finish
• An-Rotaon Micro Disc: Silver-Anodized Finish
Environmental Regulaons Complying with RoHS 3
Temperature of Usage - 35° C to 45° C
Cercaon Designed to Comply with:
• SAE J3043 (26 G)
Installaon Device Retained on Main Assembly with Support Blocks
Aachment Opons An-Rotaon Micro Disc
Transportaon Compability System Compable with Technimount's:
• Safety MD-Transporter (vercal)
• Vercal Mounng System
• Micro Base
Features • Access to all Medical Device Monitors, Connectors and Accessories
• Rubber Pads Protecng the Bracket when Placed on a Surface
• Rubber Cushions Inside the Bracket to Protect Medical Device
• An-Rotaon Micro Disc for installaon on Vercal and Wall Mounng
Systems
• Made with High-Density Aluminum
Physical Overall Dimensions Width 7.09 in, Depth 7.62 in, Height 10.14 in
Weight 2.276 lb
Part Number 770-10-LASP - Bracket Pro Serie® 77
Other Models and Conguraon Opons Contact Technimount EMS for more informaon or for other opons at
customer[email protected]
* Product and medical equipment manufacturers names are trademarks™ or registered trademarks® of their respecve holders.
Technimount does not have a commercial relaonship with these medical equipment manufacturers.

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WARNING/CAUTION/NOTE
Carefully read and strictly follow all Warnings and Cauons listed in this user guide. Servicing and maintenance should
only be done by qualied personnel.
WARNING
9Always hold the bracket with both hands when you manipulate it.
9Operate the bracket only as described in this user guide.
9Do not modify the bracket, or any components of Technimount systems. Modifying the product can cause
unpredictable operaon resulng in injury to the paent or operator.
9It is the responsibility of the operator of the bracket or any of its opons, to ensure equipment being used with the
Technimount products meets the installaon specicaons. Injury may result if non-compable products are used
with Technimount System products.
9Do not aempt to operate, install or remove the equipment while mobile. Ensure that installaon and removal of
equipment is done while vehicle or aircra is immobilized.
9Verify that the bracket is inserted correctly into a mounng system and locked. If equipment is improperly installed
and locked, it can cause the equipment to fall and cause injury to the paent or operator and/or damage to the
medical equipment.
9Never use the bracket if not properly installed and locked on a base, a cot/stretcher, or on a wall mount or oor
mount. If not installed properly, the medical device could fall during transport and may cause injury to the paent
or operator and/or damage to the product.
9Do not allow untrained sta to assist in the operaon of the mounng system. Untrained technicians/sta can
cause injury to the paent or themselves.
9Do not place addional equipment or items onto the bracket or mounts other than approved Technimount or
components, as this could damage the product and may result in injury to the paent or operator.
9Operators must be able to able to safely li the total weight of the bracket system and medical device.
9Do not aach restraints to the bracket frame. It may result in damage to the System and/or result in injury to the
paent or operator.
9Always reposion the equipment with care, avoid any improper pushing or violent manipulaon, as it may result in
unbalanced equipment and may cause injury to the paent or operator and/or damage to the product.
9Improper maintenance can cause injury to paent or operator or damage to the product. Maintain the bracket
and Mounng Systems as described in this user guide. Use only Technimount approved parts and maintenance
procedures. Using unapproved parts and procedures could cause unpredictable operaon and/or injury and will
void the product warranty.
9Failure to properly clean or dispose of corrosive products will increase the risk of premature damage and may
cause injury to the paent or operator.
9Any installaon on a surface, wall or on the structure of the vehicle has to be validated or inspected in order to
ensure it maintains the integrity of the vehicle.
SUMMARY OF SAFETY PRECAUTIONS

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WARNING/CAUTION/NOTE (CONTINUED)
CAUTION
9Only cered technical personnel familiar with the bracket installaon and use should manipulate it. Always refer
to Technimount's user guides for all instrucons for installing and using any Technimount Mounng System.
9Inspect regularly all components on the equipment for any issue and loose screws, bolts and nuts.
9Never install the mount into or on other similar mounng systems or brackets without wrien conrmaon by
Technimount System as these dierent systems may be from other brands or models and may not be compable
with Technimount Systems.
NOTE
9Some cleaning products are corrosive in nature and may cause damage to the product if used improperly. If such
products are used to clean Technimount equipment, the equipment must be rinsed with clean water and thoroughly
dried following the cleaning. Failure to properly rinse and dry the Mounng Systems will leave a corrosive residue
on the surface, possibly causing premature corrosion of crical components.
9When ordering, it is important to idenfy on which mounng system you need to mount the bracket on as there
are dierent systems for dierent applicaons (ground).
9A maintenance program should be established for all Technimount equipment. Prevenve maintenance may need
to be performed more frequently, based on the level of use of the product. Close aenon should be given to
safety features (i.e.: screws, quick release mechanisms, and aachment points).
9Failure to use authorized parts, and lubricants, could cause damage to the equipment and will void the warranty
of the product.
9This user guide should be considered a permanent part of the bracket, and should remain with the product even if
the equipment is subsequently sold.
9Technimount connually seeks advancements in product design and quality. Therefore, while this user guide
contains the most current product informaon available at the me of prinng, there may contain minor dierences
between your mounng system and this user guide.
If you have any quesons, or for more informaon, please contact Technimount Customer Service customerservice@
technimount.com.
SUMMARY OF SAFETY PRECAUTIONS

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NOTICE/CERTIFICATION
The Bracket Pro Serie® 77 is designed to comply with the essenal requirements and other relevant provisions of
the Direcve 1999/5/EC and SAE J3043. For more informaon, please contact Technimount Customer Service
([e-mail]).
Technimount E.M.S. Holding Inc.
C/O: Regulatory Aairs
3770, Jean Marchand Street, Suite 100-C
Quebec (QC) G2C 1Y6
Canada
T + 1 888.639.2758
F + 1 855.339.6351
technimount.com
[email protected]
WARNING
The end user and administrator are responsible to validate regulaons and standards for safety in their region, in
order to comply with applicable safety regulaons. Technimount is not responsible to inform the end user and/or
administrator of applicable legislaon for safety in their area.
LEGAL NOTICE
The purchase and use of products designed by Technimount are subject to this limitaon of liability. It is important to
understand that, as Technimount is not the manufacturer of the Stryker (or other brand) stretcher or the manufacturer
of the medical equipment (Dräger or other brand), Technimount cannot guarantee the resistance and durability of
such stretchers and other equipment installed on it.

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INSTALLATION GUIDE
REMOVING THE PACKAGING FOR INSTALLATION
1. Unpack boxes and check all items are included for installaon.
2. Ensure that all shipping and packaging materials have been properly removed from the product(s) prior to
installaon.
3. Idenfy all of the product components and hardware prior to starng the installaon.
4. The bracket must work properly before it is put into service.
5. Refer to the idencaon of components at the beginning of this user guide if needed.
TOOLS REQUIRED FOR INSTALLATION
Below are the basic tools required for installaon. Other tools may also be required. If you have any quesons regarding
the installaon, or need assistance, please contact our Technical Support team at [e-mail]
9Phillips Screwdriver
NOTE
9Electrical tools are not recommended, as there is a potenal risk of damage to the threads.
9Technimount provides screws for the installaon of the main assembly.
9During the installaon process, Technimount recommends the use of medium strength thread-locking adhesive
(blue Locte) to prevent the screws from loosening during normal use. Put a few drops of medium strength thread-
locking adhesive (blue Locte) on each screw before installaon.

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INSTALLATION GUIDE
IDENTIFICATION OF COMPONENTS
BOTTOM SUPPORT BLOCK
The black oxide Stainless Steel boom support block
is designed to hold Laerdal Compact Sucon Unit 4
by securing its base.
HARDWARE KIT
The following hardware is provided for the installaon
of the Bracket Pro Serie 77:
9Two (2) Black Oxide Stainless Steel Flat Head
Phillips Screws 10-32 x 1/2"
9Two (2) Black Oxide Stainless Steel Flat Head
Phillips Screws 10-32 x 3/8"

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1. The Bracket Pro Serie 77 is designed to be
installed on the Laerdal Compact Sucon Unit 4
from Laerdal.
2. Locate the medical device and boom support
block of the main assembly.
3. Align the boom of the medical device with the
boom support block.
4. Install the top part of the bracket above the
medical device, align rear vercal rods with the
mounng holes.
INSTALLATION GUIDE
INSTALLATION OF THE BRACKET ONTO THE LAERDAL COMPACT SUCTION UNIT 4

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INSTALLATION OF THE BRACKET ONTO THE LAERDAL COMPACT SUCTION UNIT 4
(CONTINUED)
5. Align the screws and screws holes of the boom
support block.
6. Install the two (2) Black Oxide Stainless Steel Flat
Head Phillips Screws 10-32 x 1/2" on the boom
support block.
7. Tighten the two (2) screws well.
8. Align the screws and screw holes at the back of
the main assembly.
9. Install the two (2) Black Oxide Stainless Steel Flat
Head Phillips Screws 10-32 x 3/8" on the main
assembly.
NOTE
Put a few drops of medium strength thread-locking
adhesive (blue Locte 242) on each screw before
installaon to prevent the screws from loosening
during normal use.
10. Tighten the two (2) screws well.
CAUTION
9Do not use electrical tools to install the screws.
9Do not overghten the screws.
INSTALLATION GUIDE

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INSTALLATION GUIDE
INSTALLATION OF THE CANISTER INTO THE BRACKET
1. Keep the strap up.
2. Install the 800ml canister into the main assembly.
3. Verify that the 800ml canister is properly installed
in the main assembly.
4. Close the strap on the canister lid and lock it.
5. Laerdal Compact Sucon Unit 4 is ready for
transport once properly inserted into its bracket
and the stretcher mounng system.

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REMOVING THE CANISTER FROM THE BRACKET
1. To remove the 800ml canister from the bracket,
li the strap on the canister lid.
2. Raise the strap completely.
3. Remove the canister from the bracket by liing it
upwards to release it.
OPERATION GUIDE