Technimount System PRO 85 Series User manual

BRACKET PRO SERIE®85
USER GUIDE

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2 BP85 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.
ESP 60™ is a registered trademark of ICU Medical.
Technimount does not have a commercial relaonship with ICU Medical. ICU Medical 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 [e-mail].
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 ICU Medical.
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 stretcher 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 techsuppor[email protected].
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 CONTENT
COPYRIGHT ............................................................................................................................................................2
Legal Notice ...................................................................................................................................................................2
CONTACT INFORMATION.......................................................................................................................................3
Symbols and Definitions ...............................................................................................................................................6
Warning/Caution/Note ................................................................................................................................................7
Product Illustration .....................................................................................................................................................8
Bracket Pro Serie 85 ..............................................................................................................................................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
Installation of the Bracket onto the ESP 60 Syringe Pump ....................................................................................16
MAINTENANCE GUIDE......................................................................................................................................... 18
Cleaning .......................................................................................................................................................................18
Cleaning Process ..................................................................................................................................................18
Removal of Iodine Compounds ...........................................................................................................................19
Preventive Maintenance .............................................................................................................................................19
Inspection Process and Schedule...............................................................................................................................20
Maintenance Program .........................................................................................................................................20
Inspection and Maintenance Record .........................................................................................................................21
Training Record ...........................................................................................................................................................22
Replacement Parts .......................................................................................................................................................23
WARRANTY .......................................................................................................................................................... 24
Warranty Policy ..........................................................................................................................................................24
Limited Responsibility and Warranty .........................................................................................................................24
International Warranty Clause .................................................................................................................................24

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TABLE OF CONTENT
RETURN POLICY ................................................................................................................................................... 25
Return Policy ...............................................................................................................................................................25
Prior to 30 Days ...................................................................................................................................................25
Prior 45 Days ........................................................................................................................................................25
Prior 60 Days ........................................................................................................................................................25
Return Authorization .................................................................................................................................................25
Damaged Merchandise ................................................................................................................................................26
Claim Process ..............................................................................................................................................................26
Required Information ..........................................................................................................................................26
Findings and Conclusion .....................................................................................................................................26
Questions about our Policy .......................................................................................................................................26

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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 85
Front View
INTRODUCTION
Top Support to Secure
Medical Device
Rubber Cushions Protecng the
Medical Device Inside the Bracket
Red Quick Release Mechanism
for Easy Installaon and
Removal of Medical Device

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PRODUCT ILLUSTRATION (CONTINUED)
BRACKET PRO SERIE 85 (CONTINUED)
Back View
INTRODUCTION
High-Density Aluminum with
Black-Anodized Finish
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 85 for the ESP 60 Syringe Pump from ICU Medical.
PRODUCT DESCRIPTION
The Bracket Pro Serie 85 is a unique soluon to mount the ICU Medical ESP 60 Syringe Pump 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
ESP 60 Syringe Pump in pre-hospital and hospital environments. The Bracket Pro Serie 85 provides a higher exibility
for dierent EMS/CCT protocols and applicaons. It is recommended for the safe transport of the ESP 60 Syringe Pump
during inter-hospital transfers for neonatal crical care.
INTENDED USE OF THE PRODUCT
The Bracket Pro Serie 85 is a mounng soluon to securely transport the ICU Medical ESP 60 Syringe Pump during
inter-hospital transfers. It is designed to be installed on the equipment as described in this user guide. The Bracket
Pro Serie 85 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® 85
Product Descripon Bracket for Transport of ESP 60™ on Stretcher during Neonatal Crical Care
Compability of Medical Device* ICU Medical® ESP 60™ Syringe Pump
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 Red Quick Release Mechanism
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 Cushions Inside the Bracket to Protect the 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 4.2 in, Depth 2.8 in, Height 11.0 in
Weight 1.96 lb
Part Number 2200-10-ESP60 - Bracket Pro Serie® 85
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 System.
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® 85 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
(customerser[email protected]).
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 stretcher 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
No special tools or equipment are required to install the medical device in the bracket.

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1. The Bracket Pro Serie 85 is designed to be
installed on the ESP 60 Syringe Pump from ICU
Medical.
2. Install the bracket on a stable surface.
3. Align the medical device with the bracket.
4. Pull and hold the Red Quick Release Mechanism
on top of the bracket.
INSTALLATION GUIDE
INSTALLATION OF THE BRACKET ONTO THE ESP 60 SYRINGE PUMP

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INSTALLATION OF THE BRACKET ONTO THE ESP 60 SYRINGE PUMP (CONTINUED)
5. Slide the medical device into the bracket.
6. Release the Red Quick Release Mechanism once
the medical device is fully inserted in the bracket
to lock it.
7. Ensure that the medical device is properly
inserted in the bracket and that the Red Quick
Release Mechanism is engaged.
CAUTION
9If the Red Quick Release Mechanism does not
fully descend, simply push lightly on the medical
device to lower it.
8. The ESP 60 Syringe Pump from ICU Medical is
ready for transport once properly inserted into
its bracket and the stretcher mounng system.
INSTALLATION GUIDE

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MAINTENANCE GUIDE
CLEANING
CLEANING PROCESS
WARNING
ENSURE TO REMOVE MEDICAL DEVICE FROM THE BRACKET IF THOROUGH CLEANING IS NEEDED.
Follow your EMS service's protocol or medical device manufacturer's user guide for the recommended cleaning
procedure of your medical devices. Cleaning procedure below does NOT provide recommendaons for cleaning of the
medical device. The following cleaning guidelines consider the Technimount mounng assemblies and components.
It is the responsibility of each hospital to use the cleaning soluon of their choice. All hospitals have policies and
procedures describing how they should clean and disinfect their medical equipment. Use a chlorine bleach soluon
(3.25% - less than one part bleach to 100 parts water), a soluon containing alcohol, phenolic cleaners (acve
ingredient - o-phenyl phenol) or a quaternary ammonium chloride soluon. In diluted concentraons, these cleaning
agents have no negave eect on our products.
The bracket can be cleaned by using a pressure washer. The bracket may show some signs of oxidaon or discoloraon
from connuous washing, however, degradaon of the product’s performance or funconality will not be aected
due to power washing if cleaning instrucons are properly followed.
The material used to manufacture the bracket is high-grade aluminum, it is very durable and resistant to corrosion,
however high levels of sodium or a high concentraon of sodium or acid may prematurely corrode the product.
Always rinse with so soap and water if exposed.
9Use of a power washer can accelerate removal of contaminants collected during the use of the product.
9Rinse with clean water.
9Towel dry all components.
9Allow all other components to air dry.
9Avoid over saturaon and ensure that the product does not stay wet longer than the cleaner manufacturer’s
guidelines for proper disinfecng.
WARNING
9When cleaning, always use appropriate personal protecon equipment (PPE) based on established protocols (e.g.,
gloves, eye wear, etc.).
CAUTION
9Do not steam clean or use ultrasonic cleaners on the system or any of its components.
9Do not immerse the metal parts/components in water.
9Maximum water temperature should not exceed 180°F/82°C.
9Maximum water pressure should not exceed 500 psi/34,5 BAR. If a pressure washer is being used to clean the unit,
the pressure nozzle must be kept a minimum of 24 inches (61 cm) from the unit.

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MAINTENANCE GUIDE
CLEANING (CONTINUED)
CLEANING SOLUTIONS
Phenolic type or quaternary type disinfectants can be used (excluding Virex® TB). Iodophor type disinfectants, Peracec
Acid, Chlorine, and especially Hydrogen Peroxide are not recommended for use because staining and corrosion may
result.
Suggested cleaners for the bracket:
9Quaternary Cleaners (acve ingredient - ammonium chloride)
9Water and so soap
9A mild 10% bleach soluon, a soluon containing alcohol or a quaternary ammonium chloride soluon. In diluted
concentraons, these cleaning agents have no negave eect on our products.
WARNING
9Some cleaning products are corrosive in nature and may cause damage to the product if used improperly.
9If the products described are used to clean the equipment, the bracket and components must be rinsed with clean
water and thoroughly dried following cleaning. Failure to properly rinse and dry the system will leave a corrosive
residue on the surface of the product, possibly causing premature corrosion of crical components.
REMOVAL OF IODINE COMPOUNDS
If rust appears on any surface of the product, we recommend sanding the aected surface to remove the rust and
then using the cleaning method presented in this guide once the rust is removed. To clean the stained area, use a
soluon of 1/4 Tablespoon of Sodium Thiosulfate in 1 pint / .5 litre of warm water to clean the stained area. Clean as
soon as possible aer staining occurs. If stains are not immediately removed, allow soluon to soak or stand on the
surface. Thoroughly rinse surfaces with clean water and allow to air dry before returning unit to service.
WARNING
9Failure to properly clean contaminated parts or components will increase the risk of exposure to blood borne
pathogens and may cause injury to the paent or the operator.
PREVENTIVE MAINTENANCE
A prevenve and regular maintenance program should be established for all Technimount equipment. Prevenve
maintenance may be required more frequently based on the usage level of the product. The bracket requires regular
preventave maintenance. Establish and follow a prevenve maintenance schedule and keep records of prevenve
maintenance acvies (see maintenance form in this user guide).
CAUTION
9Close aenon should be given to safety features including, but not limited to locking mechanisms and discs.
9Improper maintenance can cause injury or damage to the product. Maintain the product as described in this user
guide.

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MAINTENANCE GUIDE
INSPECTION PROCESS AND SCHEDULE
MAINTENANCE PROGRAM
The following inspecon roune and schedule is intended as a general guide for prevenve maintenance of the
bracket. Factors such as weather, environment, geographical locaon, and individual usage will necessitate dierent
maintenance. If you are unsure as to how to perform these maintenance inspecons or at what interval to perform
these inspecons, please contact your Technical Support Team at [e-mail]. Check each roune
and replace damaged or worn out parts if necessary
Follow metable below for maintenance (either in months (M) or hours (H)), in accordance with your Service’s current
maintenance pracces and protocols.
ITEM ROUTINE
1 M
OR
2 H
3 M
OR
6 H
6 M
OR
12
H
12
M
OR
24
H
Bracket
9Inspect the bracket
▪Inspect the screws
▪Ensure the bracket is working properly and there
are no parcles, obstacles, or debri
9Verify that the An-Rotaon Micro Disc is clean and
works properly
9Verify that the Red Quick Release Mechanism works
properly
9Do a visual inspecon of the bracket to ensure there is
no damage of chemical aack
X