Chattanooga 70005 User manual

Neo Laser
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 Laser Module Manual
13-8907 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.
0086

2
Neo Laser Module Manual
Install module from the left side (when facing the screen)
of the unit.
Items included in this module:
Laser Module – PN 70005
• Lasermodule
• ProtectiveEyewear,2Pair
• LaserInterlock
• PatientRemote,LaserInterruptSwitch
• Faceplates(tocovermoduleafterinserted)
Tools required (not included):
• #2Phillipsscrewdriver
• Standardslottedscrewdriver.
TheSystemisprogrammedtoautomaticallyrecognize
thenewModule,therefore,nosoftwareinstallationis
required.
Completethefollowingstepstoinstallthemodule:
1. Poweroffdevice.Removethepowercordfromthe
rearofthedevice.
2. Removetheblankfaceplateoverthefourthslotfrom
the front on the left and right sides of the unit. Insert
astraight-slotscrewdriverinthetopslot,pressing
downwithslightpressure.Pullthefaceplateaway.
3. Thefourthslotisillustratedbelow,butthetechnique
is the same for all modules.
4. Themodulemustbeinsertedontheleftsideinthe
fourthslotasshown.Insertthemoduleintotheslot,
with32pins(2x16)infirst.
5. Setthemoduleinplacewithgentlepressureuntilyou
feelanendpointoftravel.
MODULE INSTALLATION

3
Neo Laser Module Manual
MODULE INSTALLATION (CON’T)
Cable Insertion
ShownbelowistheCableInsertionlocation
ForcompleteUserOperatingInstructions,including
Cautions,Warnings,Dangers,Indications,and
Contraindications,refertotheUser’sManuals.
• DomesticMarket,USonly,refertoVectraNeoClinical
TherapySystemUserManual,item#13-7646(CD
Version,item#13-7647).
• InternationalMarket,refertoIntelectNeoClinical
TherapySystemUserManual,Item#13-7651(CD
Version,item#13-7652).
• Toobtainacopy,contactyourlocalrepresentativeor
DJOCustomerCare.
6. Usinga#2Phillipsscrewdriver,securethemodule
withtheprovided8-32x5/16”screwatthebottom
tab,asshown.
7. InserttheFaceplatewithconnectionopenings,
suppliedwiththemodule,ontheLeftandRightsides,
atthebottomandsnapintoplaceatthetopasshown.
8. Plugintheunitandpressthepowerbutton,allow
theunittoinitializeandthenverifythatthenewly
installedmoduleisshownasavailableontheHome
screen.

4
Neo Laser Module Manual
LASER SPECIFICATIONS
Power
Electrical Type.................................................TYPE B
Output Type ..................................... Infrared Lamp (Laser)
Laser Class....................................................... 3B
Laser Technical Specications
Pulse Frequencies........................ 8 Hz - 10000 Hz and continuous
Wavelengths......................670-950 nm (dependent on applicator)
Output......................... 100-1440 mW (dependent on applicator)
Output accuracy ................................... +/- 20% of nominal
Description of Device Markings
RefertotheDomesticandInternationalUser’sManualsfor
detailedinformationontheDeviceMarkings.
Laser Applicator Specications
ForallsinglediodeandclusterlaserandLEDapplicators,
theexpectedincreaseinthemeasuredquantitiesafter
manufacturecombinedwiththevaluesmeasuredatthe
timeofmanufactureis±20%.
Thesoftwareincorporatesacoolingfunctionthatforces
theusertocoolthelaserclusterspriortothenext
treatmentwhentreatmenttimesexceed3minutesper
application.Thesoftwarewillcalculatethecoolingtime
needed as follows:
• Fora3minutetreatment,itwillforcea15secondcool
downperiod
• Fora4minutetreatment,itwillforcea2minutecool
downperiod
• Thesoftwareextrapolatesfortimesbetween3and4
minutes
Note:Amessagewilldisplayfor5secondsonthescreen
informingtheuserthattheprobeiscoolingdownandthe
timeperiodrequired.Iftheuserattemptstousetheprobe
beforethecooldownperiodiscompleted,themessage
re-displays.Whencooldowniscomplete,amessage
displaystheunitisreadyforuse.
• Read, understand, and practice the precautionary and operating instructions.
Know the limitations and hazards associated with using any electrical
stimulation, laser device or ultrasound device. Observe the precautionary and
operational decals placed on the unit.
• 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 ClinicalTherapy 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.
DANGER
CAUTION

5
Neo Laser Module Manual
• Read, understand, and practice the precautionary and operating instructions.
Know the limitations and hazards associated with using any electrical
stimulation, laser device or ultrasound device. Observe the precautionary and
operational decals placed on the unit.
• 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 ClinicalTherapy 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.
DANGERWARNING
• 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.
• This unit is considered to be a Class 3B Laser product and thus emits
visible and invisible Laser radiation (IR). Avoid direct eye exposure to
the Laser beam. The symbol to the left is located on the back of the
applicator and indicates the active radiant surface (the area on the
applicator that emits infrared Laser energy and the direction of the
beam of light).When the unit is on, not all wavelengths are visible
to the naked eye.Therefore, when performing any operational or
functional check, always wear Chattanooga laser protective
eyewear.
• 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.
• Laser protective eyewear should be worn during laser treatment by
the operator and patient to block infrared light energy from the
eyes during treatment.
• DO NOT point the Laser beam directly into human or animal eyes.
The lens of the eye does not detect the invisible, coherent Laser
beams, potentially resulting in permanent retinal damage.
• Thisdeviceshouldbeusedonlyunderthecontinuedsupervisionofa
physician or licensed practitioner.
• Makecertaintheunitiselectricallygroundedbyconnectingonlyto
a grounded electrical service receptacle conforming to the applicable
national and local electrical codes.
• Thisdeviceshouldbekeptoutofthereachofchildren.
• UseofaccessoriesotherthanthosespecifiedinthisUserManualmay
increase electrical emissions and decrease electrical immunity of the
device.
• DONOToperatethisunitinanenvironmentwhereotherdevicesarebeing
used that intentionally radiate electromagnetic energy in an unshielded
manner.
• Cleanapplicatorsaftereachuse,otherwiseitcanleadtocross
contamination and infection.
• Intheeventofall300-Levelora200-Levelerrormessagethatcannotbe
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 a Trained
Technician before any further operation or use of the system.
• UseofasystemthatindicatesanErrororWarninginthesecategoriesmay
pose a risk of injury to the patient, user, or extensive internal damage to
the system.
• Useofcontrolsoradjustmentsorperformanceofproceduresotherthan
those specified herein may result in hazardous exposure to ultrasonic
energy.
• Disconnectthesystemfromthepowersourcebeforeattemptingany
maintenance, installation, removal or replacement procedures to prevent
electrical shock and possible damage to system.
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