Chattanooga 2090 User manual

Leading Therapy in a New

Direction!

User Manual

Model 2090

OptiFlex 3 Continuous Passive Motion Unit

TABLE OF CONTENTS

FOREWORD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

ABOUT OPTIFLEX CPM UNIT . . . . . . . . . . . . . . . . . . . . . . . . 24

Precautionary Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2

Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3

Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

Dangers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

NOMENCLATURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 511

Unit Familiarization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Pendant Familiarization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

Pendant Functions and Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-11

SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12

Additional Deﬁ nitions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12

SETUP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1316

Unit Placement and Softgoods Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . .13

New Patient Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14-15

Pediatric Footplate Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16

Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16

TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18

Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18

WARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

OptiFlex® 3 Continuous Passive Motion (CPM) Therapy Unit

FOREWORD


This manual has been written for the operators of the OptiFlex 3 Continuous Passive Motion (CPM) Therapy Unit. It contains general instructions for operation, precautionary instructions, and maintenance recommendations. In order to obtain maximum life and efficiency from your OptiFlex 3 CPM Unit, and to assist in the proper operation of the unit, read and understand this manual thoroughly.

The specifications put forth in this manual were in effect at the time of the publication. However, owing to Chattanooga Group’ s policy of continuous improvement, changes to these specifications may be made at any time without obligation on the part of

Chattanooga Group.

Before administering any treatment to a patient, you should become acquainted with the operating procedures, as well as the indications, contraindications, warnings, and precautions.

Product Description

Continuous Passive Motion is a postoperative procedure designed to aid in patient recovery after joint surgery. This unit is typically used postoperatively for total knee replacement and Anterior Cruciate Ligament (ACL) repairs. After extensive joint surgery, if a patient fails to move the joint, tissue around the joint will become stiff and scar tissue will form, resulting in a joint with limited range of motion. By repeatedly flexing and extending the affected joint through a prescribed arc of motion for an extended period of time, the

OptiFlex 3 CPM Unit lessens the adverse effects of immobilization and trauma on the knee joint.

www.ActiveForever.com

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ABOUT OPTIFLEX 3 CPM UNIT

PRECAUTIONARY INSTRUCTIONS

The precautionary instructions found in this section and throughout this manual are indicated by specific symbols. Understand these symbols and their definitions before operating this equipment. The definition of these symbols are as follows;


NOTE:

Throughout this manual “NOTE” may be found. These Notes are helpful information to aid in the particular area or function being described.

Caution-

Text with a “CAUTION” indicator will explain possible safety infractions that could have the potential to cause minor to moderate injury or damage to equipment.

Warning-

Text with a “WARNING” indicator will explain possible safety infractions that will potentially cause serious injury and equipment damage.

Danger-

Text with a “DANGER” indicator will explain possible safety infractions that are imminently hazardous situations that would result in death or serious injury.

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Read, understand and practice the precautionary and operating instructions found in this manual before operating or using the unit. Know the limitations and hazards associated with using the OptiFlex 3 Continuous Passive Motion (CPM) Therapy Unit.

Observe any and all precautionary and operational decals placed on the unit.

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Only use OptiFlex 3 on firm, flat, level surfaces.

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Extreme caution should be taken when in use with or around children.

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Use OptiFlex 3 only for its intended purpose as described in this manual.

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Turn power switch off before unplugging unit from its power source.

Do not use the cord to unplug the power cord from the unit.

Grasp at the power cord base.

Transport and store the OptiFlex 3 in temperatures between 0° and 140 °F (-18° to 60 °C) to prevent damage to the unit or its components.

Use extra care when touching metal of OptiFlex 3 after exposure to cold or heat to prevent static shock to persons and or the unit.

Condensation could result and damage OptiFlex 3 if unit is subjected to periods of low temperatures followed by periods of high temperatures.

Use care when carrying, transporting or storing the OptiFlex 3 unit to prevent damage to the unit from dropping or improper transport and storage methods.

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U.S. Federal law restricts this device to sale by, or on the order of, a physician or licensed practitioner.

Make certain that the unit is electrically grounded by connecting only to a grounded electrical service receptacle conforming to the applicable national and local electrical codes.

Keep hair, loose clothing, loose bedding, fingers and toes away from the hinge components of the unit.

Do not use the OptiFlex 3 outdoors or on wet surfaces. Use only on firm, flat, stable level surfaces to ensure stability of the unit while in operation.

Materials of the unit may become flammable or combustible if exposed to a source of ignition.

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Heat generated within the pendant may cause ignition of the pendant if wrapped in bedding or other materials.

Do not use OptiFlex 3 while smoking or around open flame.

OptiFlex 3 has been designed for protection against the exposure of urinary incontinence. Precautionary measures should still be taken when any type of liquid comes in contact with an electrical apparatus.

Always turn off and unplug unit from electrical source before servicing or cleaning. Failure to do so could result in electrical shock or personal injury.

Handle the unit only when unit is dry and hands are dry to prevent electrical shock.

Do not use the OptiFlex 3 as a toy.

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Exercise caution when using accessories and auxiliary devices such as muscle stimulators, cold packs and other modalities. Route lead wires, hoses, tubes, etc. away from the working mechanism of the

OptiFlex 3 to help prevent damage to the Optiflex 3 and any other modality used with it.

Unconscious patients or patients under heavy influence of medication must be constantly attended and monitored while the

OptiFlex 3 is in use.

The OptiFlex 3 unit must be completely visible at all times during use. Never cover the unit with bedding or any other means of concealment while in operation.

If the OptiFlex 3 is used in conjunction with the optional OptiFlex

“T” trolley, make certain the OptiFlex 3 unit is resting on the mattress of the bed and the OptiFlex “T” is suspended with no weight on the casters to prevent possible movement of the unit and or possible injury to patient.

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NOMENCLATURE

UNIT FAMILIARIZATION

Footplate Mounting Bracket

Footplate and Pendant Storage

Calf Support Assembly

Footplate Angle

Adjustment Knob


Footplate Angle

Adjustment Knob

Calf Length Adjustment

Knob (One on Each Side)

Knee Hinge

Knee Potentiometer and Hinge

Femur Hinge

Assembly

(One on

Each Side)

Motor Cover

Pendant

(See Page 6)

Transport and Storage

Handle

Unit Base Assembly

5

Thigh Adjustment Scale

Knob (One on Each Side)

Thigh

Support

Assembly

Thigh

Adjustment Scale

(cm)

(One on Each

Side)

NOMENCLATURE

PENDANT FAMILIARIZATION

Fast Back™

Carriage will slow down within 15° of the flexion angle.

Mode

Used with Fast Back, Oscillation Zone, and Progressive ROM*

Reset

Clear previous treatment settings and completed cycles.

Extension

Adjusts the extension angle.

Flexion

Adjusts the flexion angle.

Speed

Adjusts the speed of operation.

Extension/Flexion Delay

Allows user to program carriage to stop at both the extension and flexion angle for the time programmed.

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Oscillation Zone™

Carriage will oscillate three times between the flexion angle and 10° less than the flexion angle.

Progressive ROM™ *

Unit will automatically increase the programmed flexion angle by 1° every hour up to a maximum of 5° per day.

Up Arrow

Allows user to increase treatment parameters.

Down Arrow

Allows user to decrease treatment parameters.

Comfort Zone™

Temporarily decreases the flexion ROM* when discomfort is experienced.

Start/Stop

(Emergency Stop)

Start or Stop Treatment.

* Range of Motion

NOMENCLATURE

PENDANT FUNCTIONS AND USE

All user input and feedback is provided through the pendant. The following are descriptions of each button provided with OptiFlex® 3.

Extension: View and modify the extension angle parameter.

How to use: To view the extension angle, press and hold the Extension button. To modify the current extension angle, press and hold the Extension button while pressing either the Up or Down Arrow.

Flexion: View and modify the flexion angle parameter.

How to use: To view the flexion angle, press and hold the Flexion button. To modify the current flexion angle, press and hold the Flexion button while pressing either the Up or Down Arrow.

Speed: View and modify the speed parameter.

How to use: To view the speed, press and hold the

Speed button. To modify the current speed, press and hold the Speed button while pressing either the Up or

Down Arrow.

Extension/Flexion Delay: View and modify the delay time for the extension or flexion angles. Using

Extension/Flexion Delay will cause the carriage to stop at the extension and flexion angle for the time programmed.

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How to use: To view the extension/flexion delay time, press and hold the Extension/Flexion Delay button.

You can set independent Delay times for extension and flexion. If an extension and or flexion delay time is required, simply hold down the Delay button and the

Extension or Flexion button and use the Up or Down

Arrows to adjust the time.

Up Arrow: Increases treatment parameters in conjunction with other buttons.

How to use: Select the specific function to increase

(Speed, Extension, Flexion or Extension/Flexion Delay).

While pressing and holding the appropriate button, use the Up Arrow to increase the value of the specified function.

Down Arrow: Decreases treatment parameters in conjunction with other buttons.

How to use: Select the specific function to decrease

(Speed, Extension, Flexion or Extension/Flexion Delay).

While pressing and holding the appropriate button, use the Down Arrow to decrease the value of the specified function.

Reset: Resets all parameter and patient counters to factory defaults.

How to Use: To reset patient compliance counters, press and hold lightly by inserting a paper clip and accept reset by pressing the Mode button. To display total unit run time and cycles, press and hold Reset for 3 seconds, the total unit time and cycles are temporarily displayed.

NOMENCLATURE


Start/Stop (Emergency Stop): Starts or stops the treatment.

How to Use: Press the Start/Stop (Emergency Stop) button to begin or end the treatment.

NOTE: When unit is stopped and the Start/Stop

(Emergency Stop) button is pressed, the unit will immediately begin moving in the opposite direction of the last movement.

Comfort Zone™: Temporarily decreases the flexion

ROM when discomfort is experienced during treatment.

How to Use: Press and the carriage will immediately reverse direction to move toward the extension angle.

For the next five cycles, the carriage will operate in a range 5° less than the angle where the button was pressed. The Comfort Zone Flexion Angle is 5° less than the angle where the button was pressed. Once five cycles are complete, the Comfort Zone Flexion Angle will be increased by 1° each consecutive cycle until it reaches the currently Programmed Flexion Angle. See

Chart 1.

NOTE: If Comfort Zone is pressed within 30° of the currently Programmed Extension Angle, treatment will stop and the message "Comfort Zone Too Small" will be displayed.


CHART 1 COMFORT ZONE

C = Comfort Zone activated temporary flexion limit established.

5° = 5° less than the angle where Comfort Zone was activated.

Upon completion of five cycles, ROM will increase by 1° each cycle until it reaches P.

P = Programmed Flexion angle.

S = Start/Finish.

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If pain is severe, do not use the Comfort Zone function. Stop treatment immediately. Failure to stop treatment could result in tissue damage and could compromise the surgical repair.

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NOMENCLATURE


Mode: Used together with Fast Back™, Oscillation

Zone™ and Progressive ROM button to enable and disable the appropriate mode. All three modes or any combination may be used at once.

How to Use: Press Mode button along with desired function (Fast Back, Oscillation Zone and/or

Progressive ROM).

Fast Back™: When the carriage reaches 15° less than the Programmed Flexion Angle, it will begin to slow down. The deceleration rate will be half of the

Programmed Speed when the carriage comes within

10° of the flexion angle. Upon reaching the flexion angle, the carriage will reverse direction and resume the

Programmed Speed as it moves towards the extension angle. See Chart 2.

How to Use: While pressing and holding the Mode button, press the Fast Back button to enable the Fast

Back mode.

NOTE: If both Fast Back and Oscillation Zone modes are enabled, the carriage will move at the slower of 75°/ min. and half of the Programmed Speed while in the

Oscillation Zone ROM.


CHART 2 FAST BACK

Non-Working ROM

Fast Speed

Fast Speed

F = Programmed Flexion Angle

E = Programmed Extension Angle

Working ROM

(10°)

Slow Speed

Fast Speed

Working ROM

Speed = 60°/ min.

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NOMENCLATURE


Oscillation Zone™: When the carriage reaches the

Programmed Flexion Angle, it will oscillate between the

Programmed Flexion Angle and 10° less than the flexion angle, three times. The 10° range of motion is known as the Oscillation Zone ROM. While in the Oscillation

Zone ROM, the carriage will move at 75°/min. or the

Programmed Speed, whichever is slower. On the third oscillation cycle, the carriage will hold at the flexion angle for the Programmed Extension/Flexion Delay

Time. See Chart 3.

How to Use: While pressing and holding the Mode button, press the Oscillation Zone button to enable the

Oscillation Zone mode.

NOTE: If both Fast Back™ and Oscillation Zone modes are enabled, the carriage will move at the slower of 75°/ min. and half of the Programmed Speed while in the

Oscillation Zone ROM.

CHART 3 OSCILLATION ZONE

Non-Working ROM Working ROM

(10°)

Carriage oscillates

3 times before holding on the last cycle.

H = Optional Hold on Extension /Flexion Limit

*

= Start / Finish

F = Programmed Flexion Angle

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Progressive ROM™: When Progressive ROM is activated, the unit will automatically increase the

Programmed Flexion Angle by 1° every hour, up to a maximum of 5° per 24 hour period. See Chart 4.

How to Use: Press and hold the Mode button. Press the

Progressive ROM button to enable the Progressive

ROM mode. Set the desired Final Flexion Angle by pressing and holding the Flexion Button while using the Up and Down Arrows. Accept the Final Flexion

Angle by pressing the Mode Button.

NOTE: The unit must run for a full hour at the entire

ROM before the flexion angle will be increased.

Decreasing the flexion angle will automatically deactivate this mode.

CHART 4 KNEE FLEXION ROM VS. TIME

5° Increase per Day

Day 1 Day 2 Day 3 Day 4 Day 5 Day 6 Day 7

I = Initial Knee Flexion ROM

F = Final Knee Flexion ROM

ROM = I + D(n-

1

) x 5 where n is the number of days of therapy

NOMENCLATURE


Independent Delay Time

You can set independent Delay times for extension and flexion. If an extension and or flexion delay time is required, simply hold down the

Delay button and the Extension or Flexion button and use the Up or

Down Arrows to adjust the time.

Selectable Scrolling

The scrolling feature is disabled at the factory. Should you desire to enable this feature, simply press and hold the Delay and Mode buttons. The display will scroll patient data for two cycles then return to displaying Current Carriage Angle.

Patient Lock-Out

The Patient Lock-Out feature prevents the patient from changing any parameter except Comfort Zone™ and Start/Stop (Emergency Stop).

To enable the Patient Lock-Out feature: Press and hold the Up Arrow and the Mode button for three seconds. A single short beep will confirm that the feature has been activated.

Repeating the above sequence will deactivate the feature. A single short beep will confirm that the feature has been deactivated.

Language Selection

To select display language, press and hold the Mode and Extension buttons simultaneously for 3 seconds. Use and arrows to select desired language and then press Mode to accept.


Force Reversal

Force Reversal is a programmed setting that will automatically reverse the direction of the leg orthosis if the device detects a greater amount of resistance than what is programmed. Force Reversal allows you to set the amount of force required to passively move the joint without causing unnecessary pain or damage to the surgery.

The Force Reversal feature has 10 sensitivity settings, with a minimum setting of 1.

NOTE: The maximum setting of 10 is the factory default and functions as carriage obstruction.

To change the Force Reversal sensitivity setting, press and hold the

Speed and Extension/Flexion Delay buttons simultaneously and use the down arrow to decrease the sensitivity setting.

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SPECIFICATIONS

TECHNICAL SPECIFICATIONS

MODEL 2090

Input:

Weight:

Length:

Electrical Class:

100 - 240 VAC~50/60 Hz, 75 VA

27 lbs (12 kg)

37 in (94 cm)

Class I, Type B

Operation

Knee Flexion ROM Limit:

Knee Extension Limit:

Knee Speed Range :

Maximum Patient Weight:

Calf Length Range:

(knee joint to sole of foot)

Thigh Length Range:

(hip joint to knee joint)

120°

10° Hyper Extension

30°/min. to 150°/min. Nominal

350 lbs (159kg)

10 to 23.5 in (25.4 to 59.7 cm)

12 to 19 in (30.5 to 48.3 cm)

Transportation and Storage

Unit should be transported and stored within the following conditions:

Temperature:

Humidity:

0° - 140°F (32° - 60°C)

0% - 75% Relative Humidity


ADDITIONAL DEFINITIONS:

ROM- “Range Of Motion”.

Standby Power ON

Emergency Stop

Type B Equipment

Standby Power OFF

Start

Attention, Consult

Accompanying Documents

OptiFlex® 3 complies with the following Safety Standards:

UL 60601-1

CAN/CSA C22.2 No. 601.1-M90 w/AZ

IEC/EN 60601-1

IEC/EN 60601-1-2

Meets MDD 93/42/EEC, CE 0413

Type “B” Equipment, Class I

Suitable for continuous operation

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SETUP

UNIT PLACEMENT AND SOFTGOODS INSTALLATION

1. Place the unit on a level surface.

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Place the unit on a level surface. Use of the unit on unstable surfaces do not give the stability the unit requires. If the unit becomes unstable, serious injury to the patient may occur.

The Softgoods Kit is for single patient use only. A new Softgoods

Kit must be used for each new patient.

Make certain that the unit is electrically grounded by connecting only to a grounded electrical service receptacle conforming to the applicable national and local electrical codes.

2. Install the Softgoods Kit to the carriage of the OptiFlex 3. Use the

installation instructions packaged with the Softgoods kit.

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Chattanooga Group Softgoods Kit (Part Number 20533) is designed specifically for the OptiFlex 3 unit. Attempted use of any other brand of CPM Softgoods Kit may cause malfunction of the unit and injury or discomfort to the patient.

3. Plug the unit into an approved grounded outlet. Turn the power on.

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SETUP

NEW PATIENT SETUP

Reset Pendant

Depress the Reset on the Pendant

(i.e. paper clip, pen, etc.). With Reset depressed, press the Mode Button.

The Unit is now ready for new patient parameter input. Refer to pages 7 through

11.

Measuring Patient

Measure the patient from the hip joint

(greater trochanter) to the knee in centimeters.


Adjust OptiFlex Femur Component

Loosen the Thigh Adjustment Scale Knobs on each side of the unit. Raise or lower the unit to the measured distance. Tighten the

Thigh Adjustment Scale Knobs.

Placing Patient

Place the OptiFlex 3 unit, with Softgoods Kit installed, under the patient’s leg.

Align patient’s knee with the unit hinge.

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SETUP

NEW PATIENT SETUP

Securing Patient

After patient is positioned and all adjustments are made, secure the patient to the OptiFlex 3 using the strap included in the Softgoods Kit.

Starting/Stopping Treatment

After all parameters have been made, see pages 7 through 11, start treatment by pressing the Start/Stop (Emergency Stop) button.

Stop Treatment by pressing the Start/Stop

(Emergency Stop) button.

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Comfort Zone™

If the patient experiences discomfort, the

Comfort Zone button may be pressed and the carriage will immediately reverse direction and move toward the extension angle. For the next five cycles, the carriage will operate in a range 5° less than the angle where the button was pressed. Once five cycles are complete, the Comfort Zone

Flexion Angle will increase by 1° each cycle until it reaches the Programmed Flexion

Angle.

Emergency Stop

Should the patient need to stop the treatment , they may press the Start/Stop

(Emergency Stop) button once and treatment will immediately stop.

SETUP

PEDIATRIC FOOTPLATE SETUP

Pediatric Footplate

Remove footplate from unit. Lay aside for re-installation.


Loosen the footplate adjustment knobs and rotate footplate support as shown. Tighten the footplate adjustment knobs.

Re-install footplate.

Loosen the tibial adjustment knobs and pull out the footplate assembly.

Rotate the footplate assembly 180° and reinsert into the tibial adjustment tubes.

Tighten the tibial adjustment knobs.

ACCESSORIES

Patient Kits

20533  OptiFlex Patient Kit

40128  34” Strap Kit

OptiFlex 3 CPM Unit Accessories

89900  OptiFlex Bedmount

89928 – OptiFlex Storage Rack

2031 – OptiFlex T Trolley

2032 – OptiFlex Lift

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TROUBLESHOOTING


The OptiFlex 3 CPM Therapy Unit is designed with patient safety in mind. An error can be caused by both external and internal disturbances.

Before calling for service, carefully review this operator’s guide. In the event you are still unable to correct the problem, contact your Chattanooga

Group dealer for all repair service. Be certain to specify your serial number and a detailed description of the issue you encountered.

ERROR

1 & 2 Pendant isn't communicating correctly with unit.

Defective Cable, Pendant or Main

3

5

6

7

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10

11

Error reading the EEPROM on the motor pcb.

RTC battery voltage is too low indicating bad battery.

ERROR DEFINITION

A general error on the motor pcb has occurred.

Board.

PROBABLE CAUSE

Defective Cable, Pendant or Main

Board.

Pendant Battery Voltage is low.

Main Board Failure.

POSSIBLE REMEDY

• Replace the Cable, Pendant or Main Board.

• Return to Chattanooga Group for service.

• Replace the Cable, Pendant or Main Board.


• Replace the Pendant Battery.


• Replace the Main Board.


The angle pot sensor is out of range.

The angle pot is not changing when the carriage is supposed to be moving.

The motor tachometer does not match expected value.

The motor pcb has not communicated with the pendant in a reasonable amount of time.

The motor pcb was reset via the watchdog.

Carriage angle below -10° limit.

Carriage obstruction or the Angle Pot

Screw is loose.

• Loosen the Femur Adjustment Knobs. Raise the

carriage to above zero and tighten the Femur

Adjustment Knobs. Turn the unit oﬀ and Back on

with the power switch.

• Remove the obstruction.

• Tighten the Angle Pot Screw.


Main Board Failure.

Main Board Failure.





Main Board Failure.

• Replace the main board.


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MAINTENANCE

CLEANING


After each use, clean the unit using a soft cloth dampened with water and a mild antibacterial detergent.

SERVICE

Should the OptiFlex 3 CPM unit require service, contact the selling dealer or Chattanooga Group Service Department.

All returned units to the factory for service must include the following:

WARRANTY REPAIR/OUT OF WARRANTY REPAIR

1. Written statement containing the following information:

• RA Number - Obtain from factory

• Unit Serial Number

• Contact person with phone and fax numbers

• Billing address (for out of warranty repair)

• Shipping address (where to ship unit after repair)

• Detailed description of problem or symptoms

2. Copy of original invoice issued at purchase of the unit.

3. Ship unit to Factory in the original container with all accessories and information as required in item one (1) above to:

Phone: USA: (800) 592-7329

Outside USA: +1 (423) 870-7200

Outside USA Fax: +1 (423) 870-2046

Service to these units should be performed only by Service Technicians certified by Chattanooga Group.

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WARRANTY


Chattanooga Group (“Company”) warrants that the OptiFlex 3 Model 2090 Continuous Passive Motion (CPM) therapy unit (“Product”) is free of defects in material and workmanship. This warranty shall remain in effect for two years (24 months) from the date of original consumer purchase. If this Product fails to function during the two year warranty period due to a defect in material or workmanship, Company or the selling dealer will repair or replace this Product without charge within a period of thirty (30) days from the date on which the Product is returned to the Company or the dealer.

All repairs to the Product must be performed by a service center authorized by the Company. Any modifications or repairs performed by unauthorized centers or groups will void this warranty.

The warranty period for accessories is 30 days. Accessories consist of Patient Softgoods Kit shipped with the unit.

To participate in warranty coverage, this Product’s warranty registration card (included with Product) must be filled out and returned to the Company by the original owner within ten (10) business days of purchase.

This Warranty Does Not Cover:

Replacement parts or labor furnished by anyone other than the Company, the selling dealer or a certified Company service agent.

Defects or damage caused by labor furnished by someone other than Company, the selling dealer or a certified Company service agent.

Any malfunction or failure in the Product caused by product misuse, including, but not limited to, the failure to provide reasonable and necessary maintenance or any use that is inconsistent with the Product User Manual.

COMPANY SHALL NOT BE LIABLE IN ANY EVENT FOR INCIDENTAL OR CONSEQUENTIAL DAMAGES.

Some states do not allow the exclusion or limitation of incidental or consequential damages, so the above limitation or exclusion may not apply to you.

To obtain service from Company or the selling dealer under this warranty:

1. A written claim must be made within the warranty period to the Company or the selling dealer. Written claims made to the Company should be sent to:

Hixson, TN 37343 USA

Phone: USA: (800) 592-7329

Fax: (423) 875-5497

Canada: (800) 361-6661

Outside USA: +1 (423) 870-7200

Outside USA Fax: +1 (423) 870-2046

2. The Product must be returned to the Company or the selling dealer by the owner.

This warranty gives you specific legal rights and you may also have other rights which vary from state to state or location to location.

The Company does not authorize any person or representative to create for it any other obligation or liability in connection with the sale of the Product. Any representation or agreement not contained in the warranty shall be void and of no effect.

THE FOREGOING WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED, INCLUDING ANY WARRANTY

OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.

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Chattanooga 2090 User manual

Leading Therapy in a New

Direction!

User Manual

FOREWORD

Product Description

www.ActiveForever.com

MODEL 2090

Operation

Transportation and Storage

Related manuals

Chattanooga Group

OptiFlex

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