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PURPOSE OF THE DOCUMENT
This user guide is designed to assist you with the installation, operation and maintenance of the Technimount Bracket
Pro Serie 151 for the MaxBlend 2 Oxygen Blender from Maxtec.
PRODUCT DESCRIPTION
The Bracket Pro Serie 151 is a universal solution to mount the MaxBlend2 Oxygen Blender from Maxtec in different
applications such as, on surface, a vertical system, stretcher or wall systems. It is designed to securely support and
transport the MaxBlend2 Oxygen Blender in pre-hospital and hospital environments. The Bracket Pro Serie 151
provides a higher flexibility for different EMS/CCT protocols and applications. It is recommended for the safe transport
of the MaxBlend2 Oxygen Blender during inter-hospital transfers for neonatal critical care.
INTENDED USE OF THE PRODUCT
The Bracket Pro Serie 151 is a mounting solution to securely transport the Maxtec MaxBlend2 Oxygen Blender during
inter-hospital transfers. It is designed to be installed on the equipment as described in this user guide. The Bracket
Pro Serie 151 is for crew who has received the appropriate training necessary to operate the equipment in the field
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 operation of this equipment, it is highly recommended to train staff prior to use.
LIMITATION OF LIABILITY
Technimount has designed a system to attach 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 limitation 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 addition, the mounting systems are designed by Technimount to install different medical equipment. Therefore,
Technimount is not responsible for any damage that may result from the installation of multiple medical equipment
on the stretcher. For example, risks related, but not limited to, potential stretcher overloading, tipping, interference
between equipment, access restriction 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 staff and partners to use Technimount products according to the safest practices and in accordance with the
user's guide we provide. In addition, 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 confirming the purchase and accepting delivery of the transport system or any
Technimount product, this constitutes confirmation of consent to this limitation of liability clause.
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10
INTRODUCTION
BP151 UG 202108-01
www.technimount.com
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