Chattanooga 70002 User manual

Neo Ultrasound
Module Manual
Installation
Instructions
DJO , LLC
A DJO Global Company
1430 Decision Street
Vista, CA 92081-8553
T: 1-800-592-7329 USA
T: 1-760-727-1280
F: 1-760-734-5608
DJOGlobal.com
© 2017 DJO, LLC. All rights reserved.
Neo Ultrasound Module Manual
13-8911 Rev E
For complete User Operating Instructions,
including Cautions, Warnings, Dangers,
Indications, and Contraindications, refer to the
User’s Manuals.
• Domestic Market, US only, refer toVectra Neo
Clinical Therapy System User Manual, Item
#13-7646 (CDVersion, item #13-7647).
• International Market, refer to Intelect Neo
Clinical Therapy System User Manual, Item
#13-7651 (CDVersion, item #13-7652).
• To obtain a copy, contact your local
representative or DJO Customer Care.
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Neo Ultrasound Module Manual
Install the module from the left side (when facing the
screen) of the unit.
Items included in this module:
Ultrasound Module - PN 70002
• Ultrasoundmodule
• Faceplates(tocovermoduleafterinserted)
Tools required (not included):
• #2Phillipsscrewdriver
• Standardslottedscrewdriver
TheSystemisprogrammedtoautomaticallyrecognize
the new Module, therefore, no software installation is
required.
Completethefollowingstepstoinstallthemodule:
1. Poweroffdevice.Removethepowercordfromthe
rearofthedevice.
2.Removetheblankfaceplateoverthefirstslotfromthe
front on the left and right sides of the unit. Insert a
straight-slotscrewdriverinthetopslot,pressingdown
withslightpressure.Pullthefaceplateaway.
3. Thefirstslotisillustratedbelow,butthetechniqueis
the same for all modules.
4. Themodulemustbeinsertedontheleftside,intothe
first slot as shown. Insert the module into the first slot,
with32pins(2x16)insertedinfirst.
5. Setthemoduleinplacewithgentlepressureuntilyou
feelanendpointoftravel.
MODULE INSTALLATION

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Neo Ultrasound Module Manual
MODULE INSTALLATION (CONTINUED)
Cable Insertion
ShownbelowistheCableInsertionlocation.
ForcompleteUserOperatingInstructions,including
Cautions, Warnings, Dangers, Indications, and
Contraindications,refertotherespectiveUser’sManuals.
• DomesticMarket,USonly,refertoVectraNeoClinical
TherapySystemUserManual,item#13-7646(CD
Version,item#13-7647).
• InternationalMarket,refertoIntelectNeoClinical
TherapySystemUserManual,Item#13-7651(CD
Version,item#13-7652).
• Toobtainacopy,contactyourlocalrepresentativeor
DJOCustomerCare.
6. Usinga#2Phillipsscrewdriver,securethemodule
withtheprovided8-32x5/16”screwatthebottom
tab,asshown.
7. InserttheUltrasoundFaceplateswithconnection
openings,suppliedwiththemodule,atthebottom
(1)andsnapintoplaceatthetop(2),ontheLeftand
Rightsides,asshown.
8. Plugintheunitandpressthepowerbutton,allow
theunittoinitializeandthenverifythatthenewly
installedmoduleisshownasavailableontheHome
screen.
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Neo Ultrasound Module Manual
ULTRASOUND SPECIFICATIONS
Applicator Sizes
Intelect Neo:
Large Crystal........................ 0-15 W @ 1 MHz, 0-10 W @ 3.3 MHz
Medium Crystal .................................0-6W @ 1 and 3.3 MHz
Small Crystal................................... 0-3 W @ 1 and 3.3 MHz
Vectra Neo:
10 cm2Crystal....................... 0-15 W @ 1 MHz, 0-10 W @ 3.3 MHz
5 cm2Crystal....................................0-6W @ 1 and 3.3 MHz
2 cm2Crystal................................... 0-3 W @ 1 and 3.3 MHz
1 cm2Crystal.......................................0-1.5W @ 3.3 MHz
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 MHz, ± 5%; 3.3 Mhz, ±5%
Duty Cycles ................................10%, 20%, 50%, Continuous
Pulse Repetition Rate
Intelect Neo........................................16, 48, or 100 Hz
Vectra Neo ...........................................100 ± 20% Hz
Pulse Duration . . . . . . 1 mSec, ±20%; 2 mSec, ±20%; 5 mSec, ±20% Output Power
Amplitude...........................0 to 2.5 W/cm2in continuous mode,
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0-3 W/cm2in pulsed modes
Output accuracy .............................. ± 20%, 10% of maximum
Temporal Peak to Average Ratio: . . . . . . . . . . . . .2:1, ± 20%, at 50% Duty Cycle
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5:1, ± 20%, at 20% Duty Cycle
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9:1, ± 20%, at 10% Duty Cycle
Beam Nonuniformity Ratio
Intelect Neo (Measured by IEC Method) ...................6:1 maximum
Vectra Neo (Measured by FDA Method) ...................5:1 maximum
Beam Type................................................Collimating
IPXX Rating for Unit..............................................IPX0
IPXX Rating for Applicator.........................................IPX7
Treatment Time ...........................................1 to 30 min
ULTRASOUND SPECIFICATIONS (CON’T)
Head Warming Feature
The HeadWarming feature of a Neo Therapy System utilizes Ultrasound
output, resulting in warming of the Applicator to increase patient comfort.
With Head Warming enabled, ultrasound is emitted without pressing the
Start button while an ultrasound treatment is being setup. The Applicator LED
will not illuminate during the HeadWarming period. US Channel will indicate
“Head Warming”.
Output..............................0 - 50% Cycling of maximum power
Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.3 Mhz
Applicator Temperature................... 29.4 °C - 43.3 °C (85 °F - 110 °F)
Effective Radiating Areas (Vectra Neo)
ERA High ERA Low
Description ERA (cm2) cm2% cm2%
10 cm2Crystal 8.5 10 +18% 7 -18%
5 cm2Crystal 4 5 +25% 3 -25%
2 cm2Crystal 1.8 2 +11% 1.4 -22%
1 cm2Crystal 0.9 1 +11% 0.4 -55%
Effective Radiating Areas (Intelect)
Description ERA cm2 (minimum)
Large Crystal 5.0
Medium Crystal 2.0
Small Crystal 1.0

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Neo Ultrasound Module Manual
• Read, understand, and practice the precautionary and operating instructions.
Know he limitations and hazards associated with using any electrical
stimulation, laser device or ultrasound device. Observe the precautionary and
operational decals placed on the unit.
• All modalities should be routinely checked before each use to determine that all
controls function normally, especially that the intensity control does properly
adjust the intensity of the ultrasonic power output in a stable manner. Also,
determine that the treatment time control does actually terminate ultrasonic
power output when the timer reaches zero.
• Device is designed to comply with electromagnetic safety standards. This
equipment generates, uses, and can radiate radio frequency energy and, if not
installed and used in accordance with instructions, may cause harmful
interference to other devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. Harmful interference to
other devices can be determined by turning this equipment on and off. Try to
correct the interference using one or more of the following:
- Reorient or relocate the receiving device
- Increase the separation between the equipment
- Connect the equipment to an outlet on a different circuit from that to
which the other device(s) are connected and consult the factory field
service technician for help.
- Consult your authorized DJO dealer for help.
• Do not operate this unit when connected to any unit other than DJO devices or
accessories specifically described in user or service manuals.
• DO NOT disassemble, modify, or remodel the unit or accessories.This may cause
unit damage, malfunction, electrical shock, fire, or personal injury.
• Failure to use and maintain the Intelect® Neo System, its modules, and its
accessories in accordance with the instructions outlined in this manual will
invalidate the warranty.
• Use of parts or materials other than DJO’s can degrade minimum safety.
• The Intelect® Neo Clinical Therapy System is not designed to prevent the ingress
of water or liquids. Ingress of water or liquids could cause malfunction of internal
components of the system and therefore create a risk of injury to the patient.
CAUTION WARNING
• Thisdeviceshouldbeusedonlyunderthecontinuedsupervisionofa
physician or licensed practitioner.
• Makecertaintheunitiselectricallygroundedbyconnectingonlyto
a grounded electrical service receptacle conforming to the applicable
national and local electrical codes.
• Thisdeviceshouldbekeptoutofthereachofchildren.
• UseofaccessoriesotherthanthosespecifiedinthisUserManualmay
increase electrical emissions and decrease electrical immunity of the
device.
• DONOToperatethisunitinanenvironmentwhereotherdevicesarebeing
used that intentionally radiate electromagnetic energy in an unshielded
manner.
• Cleanapplicatorsaftereachuse,otherwiseitcanleadtocross
contamination and infection.
• Intheeventofall300-Levelora200-Levelerrormessagethatcannotbe
resolved, immediately stop all use of the system, and contact the dealer
or DJO for service. Errors andWarnings in these categories indicate an
internal problem with the system that must be tested by DJO or aTrained
Technician before any further operation or use of the system.
- Use of a system that indicates an Error or Warning in these categories
may pose a risk of injury to the patient, user, or extensive internal
damage to the system.
• Useofcontrolsoradjustmentsorperformanceofproceduresotherthan
those specified herein may result in hazardous exposure to ultrasonic
energy.
• Disconnectthesystemfromthepowersourcebeforeattemptingany
maintenance, installation, removal or replacement procedures to prevent
electrical shock and possible damage to system.
DANGER
• Handle, clean and dispose of components and accessories that have
come in contact with bodily fluids according to National, Local and
Facility rules, regulations and procedures.
• DO NOT connect the unit to an electrical supply without first
verifying that the power supply is the correct voltage. Incorrect
voltage may cause unit damage, malfunction, electrical shock, fire,
or personal injury. Your unit was constructed to operate only on the
electrical voltage specified on the Voltage Rating and Serial Number
Plate. Contact your DJO dealer if the unit is not properly rated.
• Device is not designed to be used in oxygen rich environment.
Explosion hazard if the device is used in the presence of flammable
anesthetic mixture with air, oxygen, or nitrous oxide.