Inventek Systems 341 Manuel D’Utilisation
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USER SAFETY INFORMATION
Cautions
This device must be installed as part of a system in conjunction with the MONITORING NODE and in
accordance to guidance and minimum characteristics per requirements provided by Mortara for deployment of
the system on the hospital/clinic’s IT network. Refer to those requirements as well as Manufacturer Disclosure
Statement for Medical Device Security (MDS2) statements provided by Mortara before deploying and using the
system.
the system on the hospital/clinic’s IT network. Refer to those requirements as well as Manufacturer Disclosure
Statement for Medical Device Security (MDS2) statements provided by Mortara before deploying and using the
system.
The device and patient cable should be cleaned between each use. Cleaning must be performed with the system
turned off and battery removed. Let all parts dry well before turning the power back on.
Prevent liquids from penetrating the system, components, or the monitor. Do not spray the system with liquid
cleaning agents. Do not allow the system, components or accessories to become in contact with unknown
substances which may compromise its mechanical or electrical integrity. If liquids have penetrated the system,
open by authorized personnel for inspection and let dry completely.
substances which may compromise its mechanical or electrical integrity. If liquids have penetrated the system,
open by authorized personnel for inspection and let dry completely.
Do not attempt to clean the telemetry device or patient cables by submersing into a liquid, autoclaving, or
steam cleaning as this may damage equipment or reduce its usable life. Wipe the exterior surfaces with a warm
water and mild detergent solution and then dry with a clean cloth. Use of unspecified cleaning/disinfecting
agents, failure to follow recommended procedures, or contact with unspecified materials could result in
increased risk of harm to users, patients and bystanders, or damage to the telemetry device.
water and mild detergent solution and then dry with a clean cloth. Use of unspecified cleaning/disinfecting
agents, failure to follow recommended procedures, or contact with unspecified materials could result in
increased risk of harm to users, patients and bystanders, or damage to the telemetry device.
No user-serviceable parts inside. Damaged or suspected inoperative equipment must be immediately removed
from use and must be checked/repaired by authorized service personnel prior to continued use.
The S2 accommodates rechargeable batteries. If the rechargeable battery appears to become defective,
refer to Mortara Technical Support.
Do not pull or stretch patient cables as this could result in mechanical and/or electrical failures. Patient cables
should be stored off of the floor away from bedrails and wheels to avoid cable damage. Roll the patient cables
into a loose loop prior to storage.
into a loose loop prior to storage.
When necessary, dispose of the telemetry device, its components and accessories (e.g., batteries,
cables, electrodes), and/or packing materials in accordance with local regulations.
Check that all operating and environment conditions such as ambient temperature meet the device’s
specifications. Allow the device to stabilize within its intended operating environment for a minimum of two
hours prior to use. Do not use the device outside the operating and environment conditions specified (section
15).
hours prior to use. Do not use the device outside the operating and environment conditions specified (section
15).
Do not exert excessive pressure on the touchscreen LCD or use a sharp or hard object with it. Excessive
pressure may permanently damage the display.
The device is UL classified:
UL-classified device in the USA and Canada.
Upon request, Mortara can supply a service manual that includes test instructions as well as a list of spare parts
that must be used with the S2.