Noninvasive Medical Technologies NMT-NCIQ1 NMT-NcIQ User Manual

Noninvasive Medical Technologies, Inc. NMT-NcIQ

User Manual

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Date Submitted2008-08-05 00:00:00
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' (GEM Noninvasiye Medical
. Technologles
NONINVASWE TECHNOLOGIES
ACROSS THE CARE CONTINUUM
‘ sigma MANUAL
Consult the operator‘s manual tor more de—
tails
Neil) is a Class II Medical Electrical Equip-
ment in which protection against electric
shock does not rely on BASiC INSULATION
only, but in which additional safety precau-
tions such as DOUBLE INSULATION or RE—
lNFORCED lNSULATlON are prcwded,
there being no provision for protective
earthing or reliance upon installation condi-
tions.
Nle uses Class BF applied parts
This equipment has been tested and/014ml to comply with the limits/pr a
Class B digital device, pursuant to Part 15 of the FCC Rules
Nclo is a prescription device to be used on
or by, the order of a Doctor or licensed
health care professional.
Noninvasive Medical Technologies, Inc.
6412 S. Arville
Las Vegas, NV 89118
Toll Free: 1—800-466-8552
Fax: 702—614-4170
www.nmtinc.org
Table of Contents
Introduction
Indications & Contraindications
Nle Kit
Physical Features
How to Use Nle
Power—Battery
How to get a measurement
Start
Set
Signal
Stick
Maintenance
Technical Specifications
Troubleshooting
NcIQ Software Installation
6-7
8-10
10
8-9
(9000000
11
12
13-14
Inroduction
The NcIQ is a transportable Non-Contact Hemod)"
namic Monitor that provides measurement of:
. Heart Rate
. Respirations
- CardiacOutput
As the monitor tracks these assessment parameters,
a Life Score number is assigned based on the change
in trend over time.
NciQ is a monitor that uses bioimpedance technology
to provide quick easy vital sign assessment in any en-
vironment. The NcIQ is NOT a medical diagnostic de-
vice. The doctor or a designated clinical professional
is responsible for interpreting what action may be re-
quired as a result of the NciCl reported values.
Indiwtions
NcIQ can be used for:
. Trauma assessment
Precautions
- Pacemakers
- Internal Cardiac Defibrillators
Contraindlcations
Nle should not be used: ‘ . .
- Directly on the skin when indiViduaIs have
skin sensitivities to adhesive material
- Directly over metallic materials suck as
Kevlar, aluminum, etc.
The Nle Kit
The Nle Kit contains the following:
. Nle Monitor —- 1
NcIQ Battery — 2
Nle Backers - 5
Nle Receiver — 1
NciQ Receiver Software — 1
Nle Physical Features
Description
The front of the NcIQ has one Start Button (1) and
one yellow light that flashes (2) when the device is
searching for a good signal. The yellow light glows
constant without flashing when a good signal is found,
indicating that the Nle should be left in place.
1. Stan Button
2. Signal Acquisition
Light
Front of the NcIQ
On the front of the Nle are a series of four
label icons that depict how to use the Nle:
0 Start
. Set
. Signal
. Stick
These are part of the label instmction, and not buttons
for use.
The back of the NcIQ has a peel off adhesive backer (3)
that attaches to textiles, clothing or the skin.
3. Adhesive Backer
How to Use the Nle
NcIQ means Noncontact IQ and can be used on the out-
side of regular clothes to monitor important vital signs, or
apply directly to the skin.
1. START— Press the start button. Depress the start
button down until it clicks and a green light will
appear underthe start button.
2. SET— When the Nle is turned on, the yellow signal
acquisition light will begin to blink. At this time the
Nle is searching for an adequate signal to meas-
ure. Hold the Nle on the center of your chest over
your clothing, or directly on the skin. When the yellow
light is flashing the NcIQ is still looking for a signal to
measure. You will also feel one small buzz which
also indicates that the Nle is searching for a good
signal.
3. SlGNAL— When the yellow light changes to a solid
steady light, then the Nle has found the correct place-
ment for signal acquisition. You will also feel three small
buzzes or vibrations from the NcIQ which means that
you need to leave the NcIQ in one spot.
4. STICK— When the yellow light quits flashing and
becomes solid, and you the three vibrations, indi-
cating that you have found the correct NcIQ place—
ment, then gently allow the NcIQ to come away
from your chest and peel back the adhesive
backer. The adhesive backer can be placed on the
outside of clothes or directly on the skin
NW»
rmfii.
Note
if the Nle loses signal acquisition the yellow light will
flash again and one short buzz or vibration can be
felt. Return the NcIQ to the spot where you last re-
ceived signal acquisition and then wait for the yellow
light to turn $0|ld and feel three short buzzes.
5. SENDING — Within minutes the MGM) is sending
your measurement parameters to the NcIQ re—
ceiver designated by the healthcare professional.
See back page for Nle receiver downloading in-
structions.
Power
Battery install
. Slide open the battery door on the bottom of
the NcIQ.
. Insert the battery pack as shown in the picture
below. .
. Replace the battery door
- Test the unit after replacing each
battery.
Maintenance
Batteries
0 Only NcIQ batteries can be used to power up the
Nle. These custom batteries can be obtained
from a certified distributor or directly from Nonin-
vasive Medical Technologies
. Nle batteries should last for eight continuous
hours of use.
. The battery charge is becoming low when the
green Start button light begins to blink. Dispose of
batteries at designated battery. disposal locations
only.
Cleaning
. The outside surface of the Nle may be cleaned
with a soft pad soaked in alcohol (95%).A new
adhesive backer should be replaced in between
patient use.
10
Technical Specifications
Meg Disposable alkaline manganese dioxide -
AAAA- 9 cells in series parallel combination.
Delivers 4.5 volts and the cell thickness
is 8.3mm,
Provides approximately 1700 milli amperes
Cell nominal voltage- 1.5 volts
Operating temperatures -OF to 130F
Shelf life — 5 years at 21 C
Enclosures: Molded painted medical grade ABS
plastic
Dimensions: (L) 3.9", (W) 3.0", (D) 0.9"
M 5.6 ounces
Adhesive Backer: Disposable hypoallergenic
Measurement Current: 210 milliamps
M 915 mHz
Output: 2.4 GHz wireless transmission
Hemodynamic Parameters Measured and Reported
- Cardiac Output
- Heart Rate
- Respiration
11
Troubleshooting
Problem
Gren Start button
Does not light up
Signal Search vibra-
tion
does not occur
Solutions
Possible Causes
Low battery Replace battery
Low battery Replace battery
NCIQ receiving soft-
ware
Does not display any
results
Low battery in . Replace comms
Comms node node battery
- Communications
frequency interfer—
ence may Prevent
the data transmis—
sion at 2.4 GHz., try
moving the comma
node closer to the
NclO . j
Nle software dis—
plays
Unbelievable results
|ncorrect chest i- Waitforsoftware
placement Niurnbers to repopu-
late
The window one
more time, if the re-
sults are still unbe-
lievable, Then repo-
sition the Nle over
the Center of the
chest per instruc-
tions and wait for the
next set of values to
repopuiate the soft-
ware window.
12
Ncht Software Installation Instructions
in order to monitor NCIQs with the NCIQ Casualty
Management software, follow these steps.
Installing the software
Insert the NCIQ Casualty Management Software CD
into your computer and complete the Setup Wizard.
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Setting up the software
To setup the program, the proper Serial Port needs
to be entered into the program under Setup, Select
[Radio Com Port] in the [Setup]
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13
dialog box will be brought up,
at nor the Serial Port connecting the Relay. then press
[ok].
Now exit the program to save the new setting. The
program only saves settings upon exit.
Operating the software .
Ensure that the Relay is powered on. Start the applica-
tion, then press the first icon on the toolbar, the green
LED style indicator above the button will light up. Now
turn the NClQ on, it should appear as [Present] in the
application.
After changing the data offset to “1” in the Options win-
dow, click “OK". Then cioee the application by clicking
the “X“ in the top right corner of the application window.
When you reopen the application, the data will be
aligned property.
14
“This equipment has been tested and found to comply
with the EMC limits for the Medical Device Directive
93/42/EEC (EN 55011 Class M & Ev 6060142). These
limits are designed to provide reasonable protection
against harmful interference in a typical medical installa—
tion. The equipment generates, uses and can radiate
radio frequency energy and, if not installed and used in
accordance with these instructions, may cause han'nful
interference to other devises in the vicinity. However,
there is no guarantee that interference will not occur in a
particular installation. if this equipment does cause
harmful interference with other devices, which can be
determined by turning the equipment off and on. the
user is encouraged to try to correct the interference by
one or more of the following measures:
. Reorient or relocate the receiving device.
. increase the separation between the equipment.
0 Consult the manufacturer or field service technician
for help.”
This device complies with part 15 of the FCC Rules.
Operation is subject to the following two conditions: (1)
This device may not cause harmful interference, and (2)
this device must accept any interference received, in-
cluding interference that may cause undesired opera-
ticn.
Any changes or modifications not expressly approved by
the party responsible for compliance could void the
user’s authority to operate the equipment,
15
Noninvasive Medical
@T Technologies
Noninvasive Medical Technologies, NC.
6412 S. Arville
Las Vegas, NV 89118
1-888-466-8552 - 702-614-4170 (Fax)
www.NMT|NC.ORG
Rev 1
9/2007

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