TECHNIMOUNT EMS Bracket Pro Series 77-FL User manual

BRACKET PRO SERIE® 77 - FL
USER MANUAL
EMS®
SAFETY AND FLEXIBILITY
WHERE IT MATTERS MOST

BRACKET PRO SERIE®77 - FL
User Manual
EMS
®
© 2023 Technimount E.M.S. Holding Inc. UM-BP77FL-202306EN-01 | Page ii of iii
Copyrights
Copyright 2023 Technimount E.M.S. Holding Inc. (Technimount EMS) is an affiliated company of Technologies
CGC Inc. All Rights Reserved. No part of this publication may be reproduced, transmitted, transcribed, stored in a
retrieval system, translated in any language, modified in any form or by any means, without the written permission
of Technimount EMS or its affiliate companies.
Trademarks
Product and medical device manufacturer names are Trademarks™ or Registered Trademarks®of their respective
holders.
-Technimount EMS®and Bracket Pro Serie®are registered trademarks of Technologies CGC Inc.
-Laerdal Compact Suction Unit®is a registered trademark of Laerdal Medical Corporation.
For any issues with your Technimount product, its components, or for any technical questions during the
installation, operation, or maintenance, please contact Technical Support at [email protected].
Contact Information
Technimount E.M.S. Holding Inc.
C/O: Regulatory Affairs
3770 Jean Marchand Street, Suite 100-C
Quebec (QC) G2C 1Y6
Canada
[email protected]
[email protected]
[email protected]
www.technimount.com
T + 1 581.700.6613
TF + 1 888.639.2758 (North America)

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User Manual
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Table of Contents
Copyrights .......................................................................................................................................................... ii
Trademarks ........................................................................................................................................................ ii
Contact Information ........................................................................................................................................... ii
1. General Mentions and Considerations ........................................................................................................... 4
........ 1.1. Intended Use.................................................................................................................................................................4
........ 1.2. User Competency ........................................................................................................................................................4
........ 1.3. Warranties .....................................................................................................................................................................4
................. 1.3.1. Warranty Policy ................................................................................................................................................4
................. 1.3.2. Limited Warranty .............................................................................................................................................5
................. 1.3.3. International Warranty Clause.......................................................................................................................5
................. 1.3.4. User Liability .....................................................................................................................................................5
........ 1.4. Claims ...........................................................................................................................................................................5
................. 1.4.1. Damaged or Defective Merchandise ...........................................................................................................5
................. 1.4.2. Return Policy.....................................................................................................................................................6
................. 1.4.3. Return of Material Authorization (RMA)......................................................................................................6
................. 1.4.4. Claim Process...................................................................................................................................................6
2. General Safety Guidelines .............................................................................................................................. 7
........ 2.1. Symbols and Definitions ............................................................................................................................................7
........ 2.2. Labels.............................................................................................................................................................................8
........ 2.3. Safety Measures ..........................................................................................................................................................9
3. Technical Specifications ................................................................................................................................ 10
4. Unpack the Mounting System ........................................................................................................................ 11
5. Bracket Pro Serie 77 - FL Illustrated Parts..................................................................................................... 12
6. Install the Laerdal Compact Suction Unit 4 in the Bracket Pro Serie 77 - FL................................................. 13
........ 6.1. Required Parts..............................................................................................................................................................13
........ 6.2. Required Tools..............................................................................................................................................................13
........ 6.3. Install the Suction Unit in the Bracket Pro Serie 77 - FL......................................................................................13
7. Maintenance................................................................................................................................................... 15
........ 7.1. Required Tools..............................................................................................................................................................16
........ 7.2. Condition-Based Maintenance Plan ........................................................................................................................16
8. Spare Parts..................................................................................................................................................... 18

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1. General Mentions and Considerations
Intended for the purchaser/supervisor, this user manual contains detailed product information and was designed
to assist with the unpacking, assembling (when indicated), and maintenance of the Bracket Pro Serie 77 - FL
mounting system. Its content should be relayed to EMS personnel during training. This document should be used
with the operating guide, which contains specific user-related information such as the operating procedures and
the daily safety checks.
NOTE: Technimount continually seeks advancements in product design and quality. While this user
manual contains the most updated product information available at the time of printing, it
may contain minor differences from the current version. For more information, please contact
Customer Service at [email protected].
1.1. Intended Use
The mounting system is designed to secure the Laerdal Compact Suction Unit 4 with 300 ml disposable canister
and tubing during air or ground EMS and critical care transport.
1.2. User Competency
The Bracket Pro Serie 77 - FL is intended for EMS personnel who have received the proper training, necessary to
operate the device in the field, according to its intended use, as outlined in this user manual and operating guide.
Please read all provided documentation thoroughly before using this device to ensure the safe operation of this
device and provide a safe environment for patients and EMS personnel.
1.3. Warranties
1.3.1. Warranty Policy
This statement constitutes Technimount’s entire warranty policy with regards to Technimount products.
Technimount makes no other warranty or representation, neither expressed nor implied, except as stated herein.
There is no warranty of merchantability or warranty of fitness for any particular purpose. Under no circumstances
will Technimount be held liable hereunder for incidental or consequential damages, arising from or in any manner,
related to sales or use of any such device.
Technimount E.M.S. Holding Inc. (Technimount) guarantees to the original "Purchaser" of the "Product" with which
this "Limited warranty" is included, that the product will be free from "Defects" in workmanship and materials under
normal use for a "Warranty period" of one (1) year from the product purchase date by the purchaser. During the
warranty period, the product will be repaired or replaced according to the "Limited warranty" without charge to the
purchaser for parts or labor. The parts and product may be repaired or replaced with new or refurbished parts or
products. Herein this Limited Warranty, "Refurbished" means parts and products which have been returned to the
factory, specifically. If the product is repaired or replaced within the warranty period, the greater of the remaining
warranty period will apply, or three (3) months from the date of repair or replacement. If the product is repaired or
replaced after the warranty period has expired, the warranty period for the repair or replacement will expire three (3)
months after the repair or replacement date.

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1.3.2. Limited Warranty
Technimount products are intended to retain medical devices in place in the case of a single crash impact.
Technimount products must not be reused if involved in a crash and must thereafter be replaced. If the end user
uses a Technimount product following a crash, it is at the end user’s own risk. Technimount will not be held liable.
The limited warranty does not apply to normal wear that could result from normal use. It does not apply when
the product or any of its components have been disassembled or repaired by someone not authorized by
"Technimount". It does not cover repair or the replacement of any product or part thereof damaged by neglect,
misuse, moisture, liquids, exposure to heat, accidents, abuse, and non-compliance with the instructions for
installation and use provided with the product.
The limited warranty does not cover physical damage to the surface of the product. The decision to repair, replace
or refuse the coverage is final and at the sole discretion of Technimount, without any compensation or obligation
from Technimount. The product defined as a "Mounting system", "Mounting solution" or "Bracket" used to attach
and secure the medical devices, is specifically designed to fulfill this requirement. Any other use will void the
warranty and Technimount shall not be held liable on any claim if the product has been modified or adapted for
use.
1.3.3. International Warranty Clause
This warranty abides by the Canadian domestic policy. Warranty outside Canada may vary by country. Please
contact Customer Service at [email protected] for more information.
1.3.4. User Liability
The purchaser and administrator are responsible to validate regulations and standards for safety in their region,
to comply with applicable safety regulations. Technimount is not responsible to inform the purchaser or the
administrator of any applicable legislation for safety in their area.
The administrator is responsible for providing proper training to any personnel who will install, operate and perform
maintenance on Technimount products.
1.4. Claims
1.4.1. Damaged or Defective Merchandise
ICC Regulations require that claims for damaged merchandise must be made with the carrier within fifteen (15)
days of the reception date. Do not accept damaged merchandise unless such damage is noted on the delivery
receipt at the time of reception. Upon prompt notification, Technimount will file a freight claim with the appropriate
carrier for damages incurred. Claims are limited in amount to the actual replacement cost. If the claim has not
been received by Technimount within the fifteen (15) day period following the date of delivery, or the damage was
not noted on the delivery receipt at the time of receipt, the customer will be responsible for the full payment of the
original invoice.
Claims for any short or broken merchandise must be made within thirty (30) days of invoicing. For details, refer to
the claim process or contact Customer Service at [email protected].

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1.4.2. Return Policy
Technimount’s mounting and bracket systems for portable medical device may be returned up to sixty (60) days
from the reception date, if:
-The received product does not match what was originally ordered.
-The product does not meet the Technimount technical sheet specifications.
-The product is not compatible with the device on which it was intended to be installed onto.
To return a Technimount product,
-A Return of Merchandise Authorized (RMA) must be requested and approved by Technimount prior to
returning the product.
-Products must be returned undamaged and in its original packaging, appropriately identified with the
approved RMA number. Returns will not be approved on a modified or damaged item.
-Charges may apply if the package received is damaged or items are missing.
-Purchaser is responsible for a restocking fee (refer to Table 1).
Table 1: Restocking fees
RESTOCKING FEES
Prior to thirty (30) days 10%
Prior to forty-five (45) days 25%
Prior to sixty (60) days 30%
For any manufacturing defect, refer to the conditions within the warranty policy or contact Customer Service at
[email protected] for additional information.
1.4.3. Return of Material Authorization (RMA)
The Technimount Customer Service department is responsible for all merchandise returns and will provide a Return
of Merchandise Authorization (RMA) number, upon approval. The RMA must be printed and placed on the returned
merchandise. Technimount reserves the right to charge shipping and restocking fees (refer to Table 1) for the
returned items. Special, modified, or discontinued items are not subject to returns.
1.4.4. Claim Process
Upon reception of the returned merchandise, a thorough inspection will be performed. If the merchandise is
compliant with the return policy or it is found that the product is defective, Technimount will take corrective
actions and close the claim. If, however, it is found that the product is not defective, but rather misused or abused,
the product will not be covered by the warranty. Details of our findings and conclusions will be provided shortly
thereafter. To submit a claim, contact Customer Service at customerser[email protected] to obtain a Return
of Material Authorization (RMA) form and return instructions.

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2. General Safety Guidelines
Pictograms, safety symbols and labels are used to alert the user to a potentially hazardous situation, which, if
not avoided, may result in minor or moderate injury to the user or patient or cause damage to the device or other
property. This includes the special care necessary for the safe and effective use of the device to avoid damage that
may occur from use or misuse. The terms "Warning" and "Caution" herein carry special meaning and should be
carefully reviewed.
WARNING -Indicates a hazardous situation that, if not avoided, could result in death or serious injury.
CAUTION -Indicates a hazardous situation that, if not avoided, could result in minor or moderate injury.
Always read and abide by all the safety guidelines identified within this document.
2.1. Symbols and Definitions
WARNING -General Warning
Alerts the reader of a potentially hazardous situation, which, if not avoided, may result in death or
serious injury to the user or patient or cause damage to the device or other property. This includes the
special care necessary for the safe and effective use of the device to avoid damage that may occur
from use or misuse.
CAUTION -Safe Working Load/Load Balance
Indicates the total maximum charge for a safe use of device.
CAUTION -General Mandatory Action
Call for action. Alerts the reader to potential risk to people not following the mandatory action
specified by the supplementary sign.
CAUTION -Follow Instructions for Use
Call for action. Reminds the reader to consult the user manual for information.

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2.2. Labels
Labelling on the surface of the Technimount product, quickly identify potential risks, contains the serial number and
provides information to the user. A manufacturing label, including the serial number (Figure 1), can be seen on the
Technimount product
1
1. Manufacturing label
Figure 1: Location of the manufacturing label (back of bracket shown)

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2.3. Safety Measures
Carefully read all safety measures herein before installing, operating, or performing the maintenance of the
Technimount product.
WARNING -Risk of Injury
Regulations and standards for safety are the sole responsibility of the end user. Ensure that the
installation specifications meet the local and regional compliance requirements before use. Product
incompatibility could cause unpredictable functioning resulting in injury to the patients or EMS
personnel.
CAUTION -Safe Handling and Operation
-The Bracket Pro Serie 77 - FL is intended for Laerdal Compact Suction Unit 4 with 300 ml
disposable canister and tubing. For a mounting system for a suction unit with a 800 ml disposable
canister, please contact Customer Service at [email protected].
-Do not modify the product, or any of its components and use only as described in this user
manual. Modifying the product or improper use could cause unpredictable functioning, resulting in
injury to the patients or EMS personnel.
-The administrator is responsible for providing proper training to any personnel who will install,
operate, and perform maintenance on Technimount products.
-Improper use of the Technimount product may damage the device or cause injury to the patients
or EMS personnel.
CAUTION -Safe Practice
-Follow the recommended maintenance plan and its guidelines, as described in the user manual
and operating guide.
-Always ensure that the medical device is secured in the bracket with all four (4) screws before use,
to prevent it from falling from the mounting system.
-Always keep the user manual and operating guide within reach of the product, even if the device
is subsequently sold, to prevent undue risk to the device, patients, and EMS personnel. The user
documentation is an integral part of the device.
-Practice installing, removing, and safely operating the medical device until the manipulations have
been perfected, before use with patients. Improper use of any Technimount product may damage
the device or cause injury to the patients or EMS personnel.
-If any serious incident occurs with the mounting solution, immediately stop using the product, and
report this incident to Technical Support at technicalsuppor[email protected] and the applicable
regulatory agency.
CAUTION -Working Load/Load Balance
The Safe Working Load (SWL) is 4.1 lb (1.86 kg). Do not overload the system.
CAUTION -Follow Instructions for Use
-Always read and abide by all the safety guidelines identified, as well as follow instructions provided
within this document.
-Refer to the manufacturer’s user manual for safety precautions and user instructions for the safe
use of the Laerdal Compact Suction Unit 4 with 300 ml disposable canister and tubing.

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3. Technical Specifications
Product Name Bracket Pro Serie®77 - FL
Description
Mounting system is designed to secure the Laerdal Compact Suction Unit®4
with 300 ml disposable canister and tubing during air or ground EMS and critical
care transport
Part Number 770-11-LASP-FL
Features -Access to the medical device's LED display, connectors, etc.
-Protective rubber cushions inside the bracket
Operating Environment EMS/CCT (Air and ground)
Compliance -Tested in compliance with FAA, 14 CFR § 23 & 27 (applicable sections)
-Tested in compliance with SAE J3043 and AMD-028
Compatible Mounting System Micro Base
Dimensions (W X D X H) 7.09 in. X 3.6 in. X 8.19 in. (18.01 cm X 9.14 cm X 20.80 cm)
Weight 1.5 lb (0.68 kg)
Composition
-Bracket: aluminum 6061-T6 with blue anodized finish
-Bottom micro disc: aluminum 6061-T6 with silver anodized finish
-Cushion: UL 94 HF-1 fire retardant EPDM closed cell foam
Safe Working Load (SWL) 4.1 lb (1.86 kg)
Operating Temperature - 31° F to 113° F (- 35° C to 45° C)
Installation Suction unit retained in mounting system by retaining frame and screws
Model & Configuration
Options
Contact Customer Service at [email protected]

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4. Unpack the Mounting System
1. Inspect the shipping box(es) for signs of damages, before accepting shipment. Take pictures and report
them promptly if applicable.
2. Move the shipping box(es) to the location of the installation.
3. Open the shipping box(es).
4. Unpack the box(es) and ensure that all shipping and packaging materials have been properly removed,
prior to installation.
NOTE: Keep all packaging material for future use.
5. Identify all the components and hardware included for installation, then set aside. Refer to Section 5 for the
illustrated parts, if needed.
6. Inspect the items for signs of damages. Take pictures and report them promptly if applicable.

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5. Bracket Pro Serie 77 - FL Illustrated Parts
3
4
1
2
5
1. Bracket Pro Serie 77 - FL
2. Retaining frame
3. Cushion (2X)
4. Bottom plate
5. Bottom micro disc
Figure 2: Bracket Pro Serie 77 - FL illustrated parts

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6. Install the Laerdal Compact Suction Unit 4 in the Bracket Pro Serie 77 - FL
6.1. Required Parts
-Bottom plate
-Retaining frame
-Phillips flat head screws 10-32 X 1 1/32 in. (4X)
6.2. Required Tools
-Phillips screwdriver #2
6.3. Install the Suction Unit in the Bracket Pro Serie 77 - FL
1. Lift the suction unit and insert it in the bottom plate, ensuring that the bottom of the medical device lays
flat and centered in the plate (Figure 3 A).
NOTE: Orient the suction unit so that the disposable canister lines up with the notch on the bottom
plate.
2. Move the suction unit back and forth, then left to right a few times to ensure it is properly inserted in the
bracket and immobile (Figure 3 B).
(A) (B)
Figure 3: Installing the suction unit in the bottom plate

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3. Insert the retaining frame over the suction unit (Figure 4 A).
4. Holding the retaining frame over the suction unit, flip the medical device on its back to access and align the
screw holes of the bottom plate and retaining frame (Figure 4 B).
5. Tighten the four (4) screws, using a Phillips screwdriver #2 (Figure 4 C) and torque by hand.
(A) (B) (C)
Figure 4: Securing the suction unit in the retaining frame
6. Lift the suction unit up on its feet. The Laerdal Compact Suction Unit 4 is ready for transport (Figure 5).
Figure 5: Suction unit installed in the Bracket Pro Serie 77 - FL

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7. Maintenance
Daily safety checks (refer to the Bracket Pro Serie 77 - FL Operating Guide) and a condition-based maintenance
plan (section 7.2) are required and should be established for all Technimount devices. Factors such as weather,
environment, geographical location and individual usage will necessitate different needs. For the maintenance of
the Bracket Pro Serie 77 - FL, follow the guidelines listed in the user manual, operating guide and in accordance
with your service’s current maintenance practices and protocols.
NOTE: Always keep records of your all maintenance activities and immediately remove defective or
expired products from your inventory.
Please contact Customer Service at [email protected] to ensure product options and availability,
or Technical Support at [email protected] for replacement parts or repair related issues.
WARNING -General Warning
-Do not perform maintenance on Technimount products, before receiving proper training.
-Perform maintenance operations, as described in this user manual. Failing to follow the
recommended maintenance plan or its guidelines could cause premature damage to the product.
-Use only Technimount parts, maintenance procedures, cleaning solutions and lubricants, as
described in this user manual. Using unapproved modified parts or procedures for the installation,
operation, or maintenance of the Technimount product may cause the device to be unstable and
could cause injury to the patients or EMS personnel and void the product warranty.
-Replace damaged or worn-out parts if past their expected service life or when damaged (refer to
the Technical Specifications in Chapter 3 of this user manual). Recycle damaged parts or dispose
according to the environmental laws that apply to your jurisdiction and consult the Safety Data
Sheets (SDS).
CAUTION -Safe Handling and Operation
-Do not steam clean or use ultrasonic cleaners on the system or any of its components.
-Do not immerse the metal parts/components in water.
-To spot clean, the maximum water temperature should not exceed 180° F/82° C. The maximum
water pressure should not exceed 1500 psi/103.5 BAR. If using a pressure washer to clean the
unit, the pressure nozzle must be kept a minimum of 24 in. (61 cm) from the unit.
-Always rinse and dry the Bracket Pro Serie 77 - FL properly after using cleaning products. Certain
types of cleaners may leave a corrosive residue on the surface of the product and could cause the
premature corrosion of critical components. Refer to the product Safety Data Sheets (SDS) for
chemical information or handling, storage and emergency measures in case of accident.
CAUTION -Corrosion
-Some cleaning products are corrosive in nature and may cause damage to the product if used
improperly. When cleaning, always use appropriate Personal Protection Equipment (PPE) based on
established protocols (e.g., gloves, eyewear, etc.).
-Dispose of corrosive wastes according to the environmental laws that apply to your jurisdiction
and consult the Safety Data Sheets (SDS).

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7.1. Required Tools
-Clean dry cloth
-Soft brush
-Power washer
-Sodium Thiosulfate solution
7.2. Condition-Based Maintenance Plan
Condition-based maintenance is carried out by the maintenance supervisor when the safety checks have revealed
underlining issues that need immediate attention and/or to prolong the longevity of the system in optimal
conditions. The maintenance supervisor should perform condition-based maintenance minimally every three (3)
months, or when required. In case of a non-conformity, immediately stop using the product and contact Technical
Support at [email protected] for a remedial action plan.
CONDITION-BASED MAINTENANCE DONE
TASKS YES NO
Safety Checks
Perform the safety checks (refer to the Bracket Pro Serie 77 - FL Operating Guide) to get an
overview of the system’s current condition.
Clean the System
1. If needed, rough clean the Bracket Pro Serie 77 - FL using a soft brush to remove grease
and dirt.
2. Remove the contaminants collected during the use of the product using a power washer.
3. Clean using a solution of 0.13 oz/3.70 ml Sodium Thiosulfate in 1 pt./0.5 L of warm water
and clean cloth. For stains, spot clean applying the solution directly on the stain and let
stand on the surface.
NOTE: Avoid over saturation and ensure that the product does not stay wet longer than
the cleaner's manufacturer guidelines for proper disinfecting.
4. Thoroughly rinse the solution with clean water and clean cloth, then towel dry all the
components before returning to service.
Condition-Based Maintenance completed on (dd/mm/yyyy), by
Comments and observations:

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CONDITION-BASED MAINTENANCE DONE

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8. Spare Parts
Technimount reserves the right to change part numbers and products without notice. Please contact Customer
Service at [email protected] to ensure product options and availability, or Technical Support at
[email protected] for replacement parts or repair related issues.
PART/KIT NUMBER PART/KIT DESCRIPTION
770-10-LASP Bracket Pro Serie®77 for Laerdal Compact Suction Unit 4 with 800 ml disposable
canister and tubing (ground EMS and critical care transport only)
Contact Customer Service Bracket Pro Serie®mounting systems

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EMS
®
Technimount EMS offers mounting solutions that can be installed
on ambulance counters, walls and stretchers which allows for
the equipment to follow the patient throughout the continuum
of care. Our unparalleled level of flexibility allows for maximum
operability in EMS, hospital and military environments.
Technimount EMS is driven to offer innovative solutions that
respond to the unique device management needs of emergency
and Critical Care Transport (CCT) teams for ground and air
ambulances. Safety is at the core of our values, all Technimount
systems are tested in compliance with the highest industry
standards for impact resistance. Technimount EMS is committed
to developing innovative solutions as healthcare practices evolve.
TECHNIMOUNT E.M.S. HOLDING INC.
3770 Jean Marchand Street, Suite 100-C
Quebec (QC) G2C 1Y6
Canada
T + 1 581.700.6613
TF + 1 888.639.2758 (North America)
technimount.com