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8

8.  AC INDICATOR LIGHT

 

Identifies that the unit is plugged into an ~ (AC) power 

source. The unit is operating on battery if this light is 

not illuminated.

9.  QUICK REFERENCE CARDS

 

Pull-out cards that contain general use instructions and 

help codes.

10.  CUFF CONNECTORS

Ports to connect hoses to cuff(s).

11.  POLE CLAMP

 

Adjustable clamp to mount the unit on a tourniquet 

stand.

2.5 SINGLE CUFF OPERATION

1.  Connect the power cord to an electrical power 

source that is compatible with the ratings listed on 

the nameplate of the unit.

2.  Connect a dual port cuff to the unit at the main cuff 

connectors.

3.  Press the ON/STANDBY touch-switch to turn the 

unit on. The unit will execute a self-check diagnos-

tic test as described in Section 2.2 of this manual. 

Successful completion of the self-check indicates 

the unit is ready for use.

 

CAUTION:

 If either cuff is pressurized to 50 mm Hg 

or more during power-up, the 

A.T.S.

 2000 Tourni-

quet will declare it an abnormal start-up sequence. 

It will assume that a surgical procedure is in pro-

cess, and will adopt pressures sensed in each cuff 

as the new set point. It will automatically go into the 

regulate mode on the cuff(s) which had the excess 

pressure. To alert the operator of this condition, the 

unit will sound a high pitch tone and illuminate the 

Alarm Silence Switch Light. The operator should 

immediately check the pressure set point and read-

just to the proper set point if necessary. The alarm 

will be cleared as soon as the set point is exam-

ined.

4.  The default settings for cuff pressure and time are 

retrieved from the nonvolatile storage during power 

up. These values may be changed prior to cuff 

inflation by following Section 2.4 step 2b.

 

For each patient, tourniquet pressure should be set 

to the minimum effective pressure. The minimum 

effective pressure should be determined by fac-

tors such as: whether the cuff is to be applied to 

an upper or lower limb; whether the limb is normal, 

hypertrophied, or obese; the patient’s preoperative 

systolic pressure; and the maximum anticipated 

rise in systolic pressure during the procedure.

5.  Prepare the patient in accordance with your estab-

lished procedures and cuff manufacturer’s instruc-

tions. The precautions of Section 1 and the follow-

ing are offered as a guide to assist in  

this process.

 

In most cases a tourniquet cuff should be applied 

to the widest part of the limb to allow as much 

tissue as possible to lie between the cuff and any 

nerves or vascular structures susceptible to dam-

age. The optimum positions are the upper arm and 

the proximal third of the thigh. In certain cases of 

forefoot surgery, the tourniquet cuff can be applied 

around the calf or to the area proximal to the mal-

leoli. For emergency surgery of the hand, a suf-

ficiently small tourniquet can be fitted around the 

wrist.

 

Apply a leak-free tourniquet cuff smoothly without 

wrinkles. The valve port and hose connections 

should be placed so that the hose will not be 

kinked when the limb is positioned for surgery. The 

limb is then prepared and draped for surgery. The 

viability of the skin and deeper tissues should be 

established prior to exsanguination of the limb and 

tourniquet inflation.

 

Exsanguinate the limb by elevating it for a minimum 

of 2 minutes and wrapping it, distal to proximal, 

using an Esmarch, Martin, or elastic bandage. The 

bandage should come up approximately to 1 in. 

(2.5 cm) from the edge of the tourniquet cuff. The 

elastic bandage is removed following inflation of the 

cuff. If regional anesthesia is being used, the anes-

thetic agent or nerve block is then administered.

 

The tourniquet time depends greatly on the 

patient’s anatomy, age, and absence of vascular 

disease. The surgeon will determine: 1. when the 

tourniquet is to be inflated; 2. to what pressure; 3. 

for how long; 4. whether to allow for intermittent 

aeration of tissues by deflating the cuff for 10 to 

15 minutes; 5. at what point in the operation the 

tourniquet should be released. In many operating 

rooms, it is customary to prominently note the time 

of inflation, and to warn the surgeon after a certain 

time has elapsed. This will allow the surgeon to as-

sess the need for further tourniquet time.

 

There is a general agreement that, for reasonably 

healthy adults, about 1 1/2 hours is safe and 2 

hours should not be exceeded without releasing the 

tourniquet to allow the underlying tissue to breathe. 

During this time, the limb should be elevated about 

60 degrees, and steady pressure should be applied 

to the incision with sterile dressing.

 

Under optimum conditions, the tourniquet cuff can 

be kept inflated until the final compression dress-

ings are in place. Postoperative swelling is then 

kept to a minimum.

6.  The cuff is inflated by pressing the MAIN CUFF 

INFLATE touch-switch. The unit will pressurize the 

main cuff to the preset pressure and start the infla-

tion clock. If the unit cannot pressurize the  

cuff to within 15 mm Hg of the set point in less then 

30 seconds, a pressure alarm will be sounded. See 

Section 2.8 for information about possible alarm 

conditions.

7.  At the end of the procedure, deflate the cuff by 

pressing the MAIN CUFF DEFLATE touch-switch. 

The PRESSURE display will show the deflation of 

the cuff, and the inflation clock will stop. Record the 

elapsed time if desired.

8. 

Remove the tourniquet cuff and any underlying 

bandages immediately following final deflation.

 

The time of tourniquet cuff removal should be not-

ed, and circulation of the limb should be checked.

9.  The time clock display(s) may be reset to zero with-

out turning the unit off. This would enable the unit to 

be used for multiple procedures without turning the 

unit off (and thus erasing the selected pressure set 

point if other than the default is used). see Section 

2.4 step 3c.

Summary of Contents for A.T.S. 2000

Page 1: ...Operator Service Manual A T S 2000 TOURNIQUET SYSTEM REF 60 2000 101 00...

Page 2: ...EDIES In no case shall Zimmer Inc be liable for any special incidental or consequential damages whether based on breach of warranty or other legal theory Some states do not allow limitations on warran...

Page 3: ...ns 6 2 3 2 Volume Selection 7 2 4 Controls Indicators and Connectors 7 2 5 Single Cuff Operation 8 2 6 Dual Cuff Operation 9 2 7 Bier Block Cuff Operation IVRA 9 2 8 Alarm Conditions 9 2 8 1 Pressure...

Page 4: ...ssis From Rear Case 24 8 10 Separating Chassis 25 11 CPU Board 26 12 Power Supply Board 27 13 CPU Schematic Sheet 1 of 3 ENCLOSED 14 CPU Schematic Sheet 2 of 3 ENCLOSED 15 CPU Schematic Sheet 3 of 3 E...

Page 5: ...s time alarm low battery voltage hardware failure For certain types of equipment mal functions the unit will also display error messages for certain equipment malfunctions that identify the cause of e...

Page 6: ...Skin grafts in which all bleeding points must be readily distinguished Compromised vascular circulation e g peripheral artery disease Diabetes mellitus The presence of sickle cell disease is a relativ...

Page 7: ...ing effect exerted by an unpressurized cuff and its padding if used which prevents venous return at the beginning of the operation 2 By blood remaining in the limb because of insufficient exsangui nat...

Page 8: ...cuff line with connector and second cuff line with connector into the reservoir sense ports See Fig 1 m Apply 250 mm Hg of pressure to the reservoir sense ports The display should read 250 3 mm Hg n...

Page 9: ...etting touch switch or The TIME display will display the time setting with an asterisk in the far left digit The asterisk helps the operator identify that the data being displayed is the set point dat...

Page 10: ...uet can be fitted around the wrist Apply a leak free tourniquet cuff smoothly without wrinkles The valve port and hose connections should be placed so that the hose will not be kinked when the limb is...

Page 11: ...Table 2 1 The appropriate actions indicated are based on the most probable causes and should only be used as a guide Other causes of alarm conditions may indicate a need for other actions In addition...

Page 12: ...ESSURIZED DURING POWER UP This will occur if for example the unit is turned off and back on without deflating the cuff STEADY HIGH PITCH CUFF INFL LIT If a cuff pressure is 50 mm Hg or greater at the...

Page 13: ...OF CALIBRATION OR CAL VALVE MALFUNCTION CAL2 FAIL STEADY HIGH PITCH LIT SECOND CUFF OUT OF CALIBRATION OR CAL VALVE MALFUNCTION CALR FAIL STEADY HIGH PITCH LIT RESERVOIR OUT OF CALIBRATION OR CAL VALV...

Page 14: ...AC power or during patient transport The Windowing Watch Dog Circuit Safety Processor is a hardware circuit that monitors the timing signal generated by the microprocessor as well as valve states and...

Page 15: ...nd 475 13 Remove source pressure then disconnect the calibra tion connecting hose from both sense ports 14 Return the set points to zero by pressing the time touch switch 3 times for each cuff 15 Pres...

Page 16: ...aintenance is required of the battery charg ing circuit The life of the batteries depends on the type of service and the storage method Battery replacement will need to be more frequent with continued...

Page 17: ...nabled TP11 5 V 0 5 V 5 V Supply TP12 5 V 0 V 0 5 V 50 mV 5 V Nominal 0 V when depressing ON STANDBY switch on membrane panel TP13 V Common 50 mV Bulk Supply Common TP14 4 5 V 0 V 1 V 50 mV 0 V if Saf...

Page 18: ...ill not inflate a Touch Switch Panel connector not properly plugged into P9 b Tubing inside unit may be pinched or improperly connected c Valve s stuck d Pump not properly plugged into P10 2 Cuff s wi...

Page 19: ...ngs b Leak in valve manifold c Transducer not working TP29 Voltage will vary with pressure 0 25 to 4 V CPU Board 13 Valve fail alarm message a Faulty valve driver b No power to valves TP17 CPU Board T...

Page 20: ...07 Valve 24 V Burkert fast inflate deflate 60 2000 000 08 Fuse 500 mA 5 x 20 mm 62 1129 001 00 Contol Panel 13 touch switch 62 1131 001 00 Alarm Silence Switch without lamp 62 1132 001 00 Alarm Silen...

Page 21: ...cm 60 7500 005 30 in 76 cm x 4 125 in 10 5 cm 60 7500 006 34 in 86 cm x 4 125 in 10 5 cm 60 7500 007 42 in 107 cm x 4 125 in 10 5 cm A T S Contour Cuff Dual Port Single Bladder 60 7500 008 42 in 107...

Page 22: ...f 60 7400 002 Contour Arm Cuff 60 7400 003 Contour Thigh Cuff 60 7400 004 Lower Leg Cuff A T S Low Pressure Cuff Dual Port Dual Bladder 60 7400 010 Cylindrical Arm IVRA Cuff 60 7400 011 Contour Arm IV...

Page 23: ...y A Reservoir Sense Ports B Main Cuff Sense Port C Second Cuff Sense Port D Calibration Hose Assembly E Calibrated mmHg Pressure Meter minimum range of 0 to 700 mmHg F Pressure Regulator 0 to 700 mmHg...

Page 24: ...ON STANDBY I O Touch Switch B PRESSURE SETTING Touch Switches C TIME SETTING Touch Switches D INFLATE DEFLATE Touch Switches E ALARM SILENCE Switch F PRESSURE Displays G TIME Displays H AC Indicator L...

Page 25: ...23 3 Block Diagram...

Page 26: ...from Rear Case 1 Remove Pole Clamp knob Removing Chassis from Rear Case 2 Remove Rear Cover Screws Removing Chassis from Rear Case 3 Remove 4 Feet and Screws Removing Chassis from Rear Case 4 Slide F...

Page 27: ...25 8 9 10 Separating Chassis 1 Remove top 2 screws Separating Chassis 3 Access to all components Separating Chassis 2 Remove Recessed Bottom 3 screws...

Page 28: ...26 11 CPU Board...

Page 29: ...27 12 Power Supply Board...

Page 30: ...manual Electrical Hazard Year of manufacture Replace fuse as marked Conformity Marking of the Council of the European Community T V Product Service Munich Germany UL Classification Mark Medical Equipm...

Page 31: ...initions 17 WARNING A T S WILL NOT DEFLATE CUFF IN STANDBY MODE MEDICAL EQUIPMENT WITH RESPECT TO ELECTRIC SHOCK FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601 1 CAN CSA C22 2 NO 601 1 A...

Page 32: ...Revised 02 05 1996 2005 Zimmer Orthopaedic Surgical Products Printed in U S A 62 2000 101 00 Zimmer Orthopaedic Surgical Products 200 West Ohio Avenue P O Box 10 Dover Ohio U S A 44622...

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