User’s Guide
REF
Integrated Power Console (IPC™) System
EC300
Symbols
EUR · USA · JPN · AUS
IPX1
EC REP
IPX7
ACC
IPX8
DEHP
STERILE
NIM
Accessory
REF
LOT
SN
REFURBISHED
!USA
On/O Button Package Contents Follow
EMC Compliance
Mark
Instructions For
Use
Do Not Oil Do Not Immerse
105345
Conforms to ANSI/AAMI ES60601-1,
Certied to CAN/CSA-C22.2 No.60601-1,
IEC/EN 60601-1
Caution: Federal law (USA) restricts this device
to sale by or on the order of a physician.
>120 VAC
ON
<120s
Fuse
Use By Date
Accessory
AC Power Type BF Applied Part Foot Pedal
Output Start/Stop Fine Irrigant
Is Approximately
Equal To
Non-Sterile Consult Instructions
Non-Sterile
Quantity
Not Greater Than
120vac
Caution
Applied Part
OFF
Duty Cycle
>180s
Catalog Number Manufacturer
Lot Number
Serial Number Ergonomically
XX° C
>X° C
BUR
EHS
Fr
Protected Against
Vertical Water Drops
Protected Against
The Eects Of
Temporary
Immersion In Water
Protected Against
The Eects Of
Temporary
Immersion In Water
RF Transmitter
(Interference May
Occur)
for Use
Stim Bur Connector
NIM Console
Connector
Electrical High
Speed Handpiece
Connector
World Wide Standard
for Medical Tubing
Diameter
Date of Manufacture Handpiece
<XX° C
Temperature
XX° C
Limitation
Outer Limits =
Transport
Inner Limits = Use
Engineered
F
R
1
2
Oscillate
Forward
Reverse
Connector
Adjustment
Left Foot Control
Unit Button /
Mode Button
Right Foot
Control Unit
Button / Control
Button
Top Foot Control
Unit Button
/ Handpiece
Button
Locked
Unlocked
Pump Head 1
Pump Head 2
Refurbished
Authorized Representative in the European
Community
Precaution: Pinch Hazard. Keep Fingers Clear
Of Rollers
PHT
Contains DEHP (di-2-ethyl hexyl phthalate)
Protective Earth
Equipotential Ground Connector
Use With
RoHS - Environmental friendly use period China (SJ/T11364-2006)
Do Not Dispose Of This Product In The
Unsorted Municipal Waste Stream. Dispose Of
This Product According to Local Regulations.
See
Recycling.Medtronic.com for Instructions On
Proper Disposal Of This Product.
If the single use symbol is on the device
label then this device is designed for single
patient use only. Do not reuse, reprocess, or
resterilize this product. Reuse, reprocessing, or
resterilization may compromise the structural
integrity of the device and/or create a risk of
contamination of the device, which could result
in patient injury, illness, or death.
Adapter
Attachment
Bone Mill
Brush
Control Unit
Dissecting Tool
Instrument Case
Lubricant/Diuser
Motor
Multi-Use Disposable Attachment
Regulator
USA Only Speed Range
<NNNN
min
For use up to
“NNNN” RPM
Table of Contents
Symbols .......................................................................................................................................................... 2
IPC™ System .................................................................................................................................................... 4
Glossary ............................................................................................................................................................................................................................... 4
Indications for use ...........................................................................................................................................................................................................4
Device description ........................................................................................................................................................................................................... 4
Contraindications ............................................................................................................................................................................................................4
Additional IPC™ congurations ..................................................................................................................................................................................4
Warnings .............................................................................................................................................................................................................................4
Precautions .........................................................................................................................................................................................................................5
System requirements and specications ................................................................................................................................................................5
System sounds ..................................................................................................................................................................................................................6
System gures ...................................................................................................................................................................................................................7
Pre-and Post-operating instructions ...................................................................................................................................................................... 10
IPC™ components ......................................................................................................................................................................................................... 12
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity ............................................................................................... 13
Limited warranty ........................................................................................................................................................................................................... 15
For items contaminated with TSE agents ............................................................................................................................................................ 15
Troubleshooting ........................................................................................................................................... 16
Error codes .................................................................................................................................................... 18
Cleaning and sterilization ............................................................................................................................ 20
Customer service .......................................................................................................................................... 21
Integrated Power Console (IPC™) System
IPC™ SYSTEM
IPC™ System
Glossary
The following words and acronyms may be used in this guide.
FCU Foot Control Unit
FWD Forward - Rotation is clockwise
I.V. Intravenous
IPC™ Integrated Power Console
OSC Oscillate
REV Reverse - Rotation is counter-clockwise
Tool Surgical cutting device
Motor Handpiece/drill
Accessory Any compatible product that can be used with the IPC™
Attachment Any compatible product that can be secured to a handpiece
Indications for use
The IPC™ is indicated for the incision/cutting, removal, drilling, and sawing of soft and hard tissue and bone, and biomaterials in Neurosurgical
(Cranial, Craniofacial), Orthopedic, Arthroscopic, Spinal, Sternotomy, and General surgical procedures.
Device description
The IPC™ System is a powered drill and saw system that will remove soft tissue, hard tissue and bone during surgical procedures. The system
consists of a power control console, foot pedal, connection cables and assorted handpieces to drive various burs, blades, drills, rasps, cannulae
and saws. It includes integrated irrigation pumps for irrigation of blades, burrs and for motor or attachment coolant.
Contraindications
The IPC™ System is contraindicated for arthroscopic microdiscectomy in individuals with the following:
• Severe/progressive neurological decits
• Cauda equine syndrome
• Active infection
Arthroscopic microdiscectomy is not indicated for individuals with sequestered disc fragments, discogenic pain, internal disc destruction, or
lumbago.
Additional IPC™ congurations
Additional IPC™ congurations are available. Refer to the following User’s Guides for related information.
• IPC™ System Model: 1898001 (CFN 1898851)
• IPC™ System Model: 2340000 (User’s Guide M976332A001)
Consult the appropriate User’s Guide for indications, contraindications, warnings, and component information specic to each system.
Warnings
System warnings
W1 It is important that the IPC™ system operator be familiar with the system User’s Guide, its precautions, procedures and safety issues.
W2 Do not use the IPC™ system in the presence of ammable anesthetics. Avoid potential ignition or explosion of gases.
W3 To avoid the risk of electric shock, this equipment must only be connected to a supply main with protective earth.
W4 To avoid the risk of electrical shock, achieve electrical grounding reliability with proper connections. Connect the IPC™ system to hospital
grade receptacles only.
W5 Do not attach any system component or accessory other than Medtronic approved components to the IPC™ system as this may result in
electrical shock, component damage, substandard performance, increased emissions, or decreased immunity.
W6 Disconnect power to the IPC™ system before cleaning the unit to avoid electrical shock.
W7 This medical device complies with EN60601-1-2 safety standard for electromagnetic compatibility, requirements and test. However, if this
equipment is operated in the presence of high levels of electromagnetic interference (EMI) or highly sensitive equipment, interference may
be encountered and the user should take whatever steps are necessary to eliminate or reduce the source of the interference. Diminished
performance may lengthen operating time for the anesthetized patient.
W8 Do not operate the IPC™ system in the presence of Magnetic Resonance Imaging devices.
1-4
Integrated Power Console (IPC™) System
IPC™ SYSTEM
W9 Medical Electrical Equipment needs special Precautions regarding EMC and needs to be installed and put into service according to the EMC
information provided in this Guide.
W10 The IPC™ system should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the IPC™ system
should be observed to verify normal operation in the conguration in which it will be used.
W11 Portable and mobile RF communications equipment can aect Medical Electrical Equipment.
W12 Keep NIM™ Muting Probe cable away from IPC™ system cables to prevent unintended EMG interference or muting.
W13 After each procedure, properly clean all reusable system components.
W14 All service must be performed by Medtronic qualied personnel only. Repair and/or modication to the IPC™ system by anyone other than
qualied service personnel may signicantly compromise the unit’s ability to perform eectively and/or void the equipment warranty.
W15 Auxiliary Power Outlet with protective cover is for use with the Hydrodebrider or Bone Mill only. Consult Hydrodebrider and Bone Mill
instructions prior to use.
Precautions
P1 Do not kink cables. Inspect cables and pins for cracks, tears or corrosion.
P2 When using a Y-Splitter, only one multifunction foot pedal shall be active at a time.
P3 Do not connect multiple Y-Splitters.
P4 Remove and discard accessories following local regulations for proper disposal of contaminated materials.
System requirements and specications
Console Specications
Functional Standards for Electrical Systems
ANSI/AAMI ES60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential
performance
IEC 60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential
performance
EN 60601-1 Medical electrical equipment - Part 1: General requirements for basic safety and essential
performance
IEC 60601-1-4 Medical electrical equipment - Part 1: General Requirements for Safety, Part 4: Programmable
Electrical Medical Systems
IEC 60601-1-2 Medical electrical equipment - Part 1-2: General Requirements for Safety - Collateral Standard:
Electromagnetic Compatibility - Requirements and Tests
CAN/CSA C22.2
#60601-1
Medical Electrical Equipment - Part 1: General Requirements for basic safety and essential
performance
2005, 2012
2005, 2012
2006, 2014
1996, 1999
2007, 2014
2005, 2014
Physical Dimensions
Size 277 mm Width x 353 mm Height x 267 mm Depth
Weight 7.3 kg
Operational Environment
Temperature +10 °C to +33 °C
Humidity 30 % to 75 % RH
Barometric Pressure 700 - 1060 hPa
Transport and Storage Environment
Temperature -40 °C to +70 °C
Humidity 10 % to 95 % RH
Barometric Pressure 500 to 1060 hPa
Display / Touchscreen
Type High contrast, digital, graphic color, visible in complete darkness
Resolution Display 21 cm diagonal, resolution 480 X 640 pixels
Audio Output
Baseline Audio Sound Level 60 dBA minimum SPL (1 m)
Integrated Power Console (IPC™) System
1-5
IPC™ SYSTEM
Electrical
Input Voltage 100 V-240 V ± 10%
Frequency 50/60 Hz
Power Consumption 500 VA
Auxiliary AC output 200 VA Max.
Internal Fuse 5 x 20 mm T. L. 5 A, 250 V
Medtronic Xomed P/N 11270066
Duty Cycle for Applied Part Maximum On Time 120 Seconds
Minimum O Time 180 Seconds
System power cords
Region Part Number Region Part Number Region Part Number
USA, Barbados, Belize,
Bolivia, Canada,
Colombia, Ecuador,
Venezuela
China EA604 India, South Africa EA607 Switzerland EA601
Argentina EA608 Israel EA609 Denmark EA610
Australia, New Zealand EA605 Japan EA603 or 1895823 Italy, Chile EA611
Standard
EA600 or 1895820
6 meter
EA650 or 1897821
United Kingdom,
Ireland, Hong Kong,
Malaysia, Singapore
EA606 Austria, Belgium, Finland,
France, Germany, Greece,
Korea, Luxembourg,
Netherlands, Norway,
Portugal, Spain, Sweden
EA602 or 1895822
System sounds
The following tones can sound while using the IPC™ Console.
IPC™ Tone Cause(s)
1 Tone • Conrmation of change button pressed.
• Change from Forward to Oscillate.
• Change of active handpiece.
2 Tones Change from Oscillate to Forward.
3 Tones • Audible Alarm. Error detected. See screen for error message.
• Active handpiece is in Reverse and foot pedal pressed.
• First time accessory changes from Forward to Reverse.
Long Tone Change from handpiece to drill.
1-6
Integrated Power Console (IPC™) System
System gures
12
IPC™ SYSTEM
Figure 1-1. IPC™ Console Front
1
2
3
4
5
1 Pump 1: Coolant, irrigation
2 Touchscreen
3 Power on/o
4 Pump 2: Irrigation
5 Console connector panel for peripheral devices
Figure 1-2. IPC™ Console Back
1
2
3
4
5
67 8
1 Pole clamp
2 Compact ash card port (Medtronic Use)
3 Manual start/stop
4 Auxiliary power outlet
5 Endo-Scrub 2 connector
6 Fuse access
7 Equipotential Ground Connector.
Apply potential equalization conductor.
8 Hospital grade power cord connector
1 Legend EHS™ 4 Stimulus input from patient interface
2 Legend EHS™ Stylus, Stealth-Midas™ 5 Stimulus output to stim bur guard or
3 Midas Rex™ Stylus Touch™ motor,
Microsaws, High-torque handpiece,
and MR8 motors
Integrated Power Console (IPC™) System
Figure 1-3. IPC™ Console Connector Panel
3567 8
4
(NIM™ or NIM-Eclipse™)
POWEREASE™
6 Not applicable
7 IntelliFlow™ irrigation remote control
8 Multifunction foot pedal
Figure 1-4. Multifunction Foot Pedal & Y-Splitter
1
5
4
2
3
1
5
1 Mode button 5 Foot pedal
2 Handpiece button 6 Y-Splitter
3 Control button 7 Port 1
4 Slip-resistant foot pad 8 Port 2
6
7
8
2
4
3
1-7
IPC™ SYSTEM
Figure 1-5. IPC™ Touchscreen
Figure 1-6. IPC™ Pumps Screen
1
Speed
2
3
4
5
1 Displays active handpiece 5 Opens Help screen
2 Accessory control panel 6 Inactive handpiece
3 Foot pedal variable control 7 Set active handpiece settings as default
4 Opens Pumps screen
Acceleration
Pump 2
Pumps
?
?
Help
Handpiece Name
+
60000
100
+
+
%
+
+
0
cc/min
+
RPM
Prime
(Handpiece Name)
Control
Finger
Mode
FWD
REV
Foot
Both
Prime
Pump 1
None
None
3
7
6
4
1 Close Pumps screen 3 Pump 1 panel available accessories
2 Prime/Flush pump 4 Pump 2 panel available accessories
Pump 2
None
None
M4
M4
Irrigation
Irrigation
Prime
Endo-Scrub® 2
Endo-Scrub® 2
Prime
Endo-Scrub® 2
Endo-Scrub® 2
1
2
Figure 1-7. Operating Room Setup
3
2
1
10
4
9
7
8
1 Mode anesthesia equipment 6 Microscope
2 IPC™ system 7 Surgeon
3 Nursing supplies/Surgical
instruments
4 Scrub nurse 9 Anesthesiologist
5 NIM™ Monitor 10 Patient
1-8
8 Electro-Surgical unit
5
6
Integrated Power Console (IPC™) System
Figure 1-8. IPC™ System Conguration
1
IPC™ SYSTEM
Figure 1-9. IntelliFlow™ Remote Control
1
2
2
3
11
3
4
10
9
5
6
8
7
1 Irrigation and coolant bags 7 Irrigation pole base diameter
2 Irrigation pole 8 Irrigation pole basket
3 IPC™ console 9 Power cord
4 Console connector panel 10 Pump 2
5 Accessory cables 11 Pump 1
6 Console height
1 Pause/On-O
2 Increase/Decrease Fine Adjustment
3 Increase/Decrease Coarse Adjustment OR
Select stainless steel tubing size (French size) for suction
irrigator.
Integrated Power Console (IPC™) System
1-9
IPC™ SYSTEM
Pre-and Post-operating instructions
The following are general IPC™ pre- and post-operating instructions. Refer to other sections of this User’s Guide for operating instructions
specic to individual handpieces or accessories.
When the system arrives
• Verify the contents of the box match the packing slip. If incomplete or damaged, notify Medtronic Customer Service.
• If container is damaged, or cushioning material shows stress, notify carrier and Medtronic Customer Service. Keep shipping materials for
carrier inspection.
• Save the cartons and packing material. If the instrument is to be shipped the shipping package will provide proper protection.
Set up the IPC™
Refer the related topics for detailed instruction.
1. Install pump cartridges or irrigation tubing.
2. Prepare IPC™ for use.
3. Calibrate touchscreen, if necessary.
4. Change system settings, if necessary.
5. Set up and prime pumps.
6. Conrm system operation.
7. Press the manual start/stop button on the back of the console (Figure 1-2) and verify you can start/stop the handpiece, irrigation and/or
coolant ow.
Install the pump cartridges or irrigation tubing
The pumps are available for use with accessories requiring irrigation or cooling.
1. Locate the correct pump and lift up the lock (Figure 1-10).
Pump 1: Coolant, lens cleaning or irrigation
Pump 2: Irrigation
Note: The number on the pump must match the number on the cartridge (either 1/1
or 2/2). If the cartridge does not have a pump designator number, use the Pump Setup
Screen to install the pump cartridge.
2. Insert the pump cartridge.
3. Snap the pump lock shut.
Note: Ensure the pump cartridge does not crimp the tubing.
Figure 1-10. Install Pump Cartridge
1
2
3
Prepare IPC™ for use
1. Verify Operation Room set up (Figure 1-7). The surgeon may have preferences to the location and visibility.
2. Verify the wheels are locked on the IPC™ cart.
3. Inspect all components for damage and determine if the system is ready for use.
4. Mount the IPC™ and irrigation/coolant bags on the I.V. pole (Figure 1-8).
Notes:
• Mount irrigant and coolant bags above the IPC™ to ensure adequate ow.
• It is recommended to use an irrigation pole with minimum base diameter of 53 cm and to mount all items as low as possible to increase
stability during use.
• For transport or uneven oor conditions greater than 10 degrees, maximum height to mount the console is 38 cm if irrigation and coolant
bags are at fully extended pole height.
5. Plug the IPC™ into the power source. Position the IPC™ so that it does not obstruct the power source for the purpose of disconnecting the
Main voltage by the power cord.
6. Locate the correct foot pedal or accessory connection port on the connector panel (Figure 1-3), align the mark on the connector to the mark
on the console, and then insert the connector.
7. Connect suction, cooling and/or irrigation tubing.
8. Turn on the IPC™ and verify the system passes the self-test and the accessory screen appears on the IPC™ monitor.
Note: If the IPC™ does not detect a handpiece or foot pedal the Connect Handpiece/Connect Foot Switch screen appears. Do the following:
• Verify the cable is connected to the correct connection port.
• Press [OK] in the Connect Handpiece/Connect Foot Switch message window to continue use of the IPC™ without the handpiece or foot
pedal.
1-10
Integrated Power Console (IPC™) System
IPC™ SYSTEM
Calibrate touchscreen
Note: This step is optional.
1. Turn on the IPC™ console.
2. When the system starts, on the Splash screen, press [Settings].
3. On the Settings screen, press Touch Screen Calibration and follow the screen prompts.
Change system settings
Note: During surgery, system settings can be overwritten.
1. Turn on the IPC™ console.
2. While the system starts, on the Splash screen, press [Settings].
3. To change the language, press the appropriate language.
4. To change the default settings, press [Default].
• On the Default screen, press the Forward or Backward arrow to change the accessory.
• Make changes to the default settings.
• To conrm system settings and return to the Splash screen, press [OK].
5. For accessories with audible tones, press the REV Audible Tones button to control the following:
• The system delivers one set of reverse beeps when the Reverse mode is activated.
• The system delivers one set of reverse beeps the rst time the drill is used in Reverse mode after the Reverse mode has been activated.
6. To conrm system settings and continue to the IPC™ touchscreen, press [OK].
7. To restore settings to factory default, press [Restore].
Set up and prime pumps
• The IPC™ turns on pump 1 and/or 2 long enough to purge air out of the tubing set(s) the rst time the prime button is pressed.
• The IPC™ resets the prime feature when you turn IPC™ power O and On.
• After you prime the pump, the prime button and functionality become ush functionality.
1. Connect tubing from an IPC™ cartridge to irrigation or coolant port on an accessory.
2. On the irrigation tubing, turn the clamp to OPEN.
3. If an accessory uses the clear drip chamber (Visao), ll the clear drip chamber with coolant. To ll, squeeze and release the chamber until full.
4. On the IPC™ touchscreen (Figure 1-5), press the pumps button.
Note: The IPC™ pumps screen is also available from the Connect Handpiece/Connect Foot Switch screen which the system displays during
IPC™ preparation for use if a handpiece or foot switch is not detected by the system.
5. On the IPC™ pumps screen (Figure 1-6), select the accessory for each pump.
6. For each pump, press the prime button and verify the following:
• Pump(s) run until air is completely purged from tubing.
• Small amount of lubricant ows at the tip of the irrigation device.
• Pump(s) turns o.
7. Press the close button.
Pump default congurations
The pump conguration is dependent on the handpiece(s) connected to the console. The following table denes the pump default settings (X)
and default options (O).
Handpiece Cooling Irrigation Irrigation Pump 1 Pump 2 Pump 1 Pump 2
Stylus Touch™ X O O O O O
Legend EHS™, Legend EHS™
Stylus, Stealth-Midas™ and
MR8 motors
Midas Rex™ Microsaws O X O O O O
* When the IPC™ detects both the Endoscrub 2 and the Stylus Touch™, and the Legend EHS Stylus, or Midas Rex™ MR8, Midas
Rex™ MR8 Plus, Midas Rex™ MR8 Touch, or Stealth-Midas™ MR8, by default, the system sets pump 2 as a “shared” irrigation
pump. You must manually connect the irrigation tubing to the active handpiece.
Integrated Power Console (IPC™) System
Table 2. IPC™ Pumps Screen Default Congurations
Pump 1 Pump 2 Endo-Scrub 2 Suction Irrigator
X O* O O O O
1-11
IPC™ SYSTEM
+
+
Conrm system operation
1. Conrm the irrigation pedal starts handpiece and irrigation ow. Verify the speed changes from white to yellow in the Speed box on the
touchscreen.
2. Conrm the foot pedal buttons operate. Refer to Multifunction foot pedal for details.
3. On the touchscreen, verify you can do all of the following:
• Adjust Speed: In the Speed box, press the plus and minus buttons.
• Change Modes: In a Mode box, press any mode button.
• Adjust Flow Rate: In the Irrigation box, press the plus and minus buttons.
+
+
Disassemble the IPC™
1. Remove irrigation tubing or cartridge from IPC™ pump.
Note: Before removing the tubing from the pump, adjust the clamp on the intravenous tubing to the CLOSED position to prevent excessive
drainage of irrigant from the intravenous bag.
2. Disconnect components and cables. To disconnect non-silicone multi-pin cables from the console, push the cable toward the console and
then pull out by the lock ring.
Note: Silicone insulated multi-pin and single pin cable connectors do not have a lock ring. Remove these types of cable connectors straight
from the connector panel.
3. After disconnecting insulated connectors from the console, connectors that have debris under the insulator must be cleaned according to
Cleaning and Sterilization instructions. If debris is still present after cleaning and sterilization, return for warranty servicing.
4. See Cleaning and sterilization section of this User’s Guide for instructions.
IPC™ components
Auxiliary power to console
Note: The auxiliary power outlet is available for use with the Hydrodebrider™ and Bone Mill consoles only.
The auxiliary power outlet is for use at grid voltage ≤120 VAC only.
Multifunction foot pedal
You can use the multifunction foot pedal (Figure 1-4) to start/stop the handpiece, control handpiece speed, handpiece selection and mode of
operation. Refer to the Multifunction foot pedal controls topic for each handpiece for specic use and control.
Y-Splitter
Y-Splitter (Figure 1-4) allows using a maximum of two multifunction foot pedals connected to a single IPC™. In this conguration, the Y-Splitter
shall be connected to the IPC™, and the multifunction foot pedal(s) shall be connected to the Y-Splitter. When connecting a single foot pedal to
the Y-Splitter, you may connect to either Port 1 or 2.
IntelliFlow™ irrigation remote control
Use the IntelliFlow™ irrigation remote control (Figure 1-9) to start/stop and change irrigation ow while in the sterile eld.
If you are using handpiece irrigation:
• To pause irrigation ow, press the Pause/On-O button.
• To adjust ow rate, press the Fine Adjustment or Coarse Adjustment Increase/Decrease button.
If you are using the Suction Irrigator:
• To pause or turn on/o the Suction Irrigator, press the Pause/On-O button.
• To adjust ow rate, press the Fine Adjustment Increase/Decrease button.
• To select the stainless steel tubing size (French size), press the Stainless Steel Tubing Size button.
1-12
Integrated Power Console (IPC™) System
IPC™ SYSTEM
Electromagnetic compatability
Environment of Intended Use: Professional healthcare facility environment
Guidance and manufacturer’s declaration – electromagnetic emissions
The IPC™ System is intended for use in the electromagnetic environment specied below. The customer or the user of the IPC™ System should assure that it is used in such an
environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic
emissions
IEC 61000-3-2
Voltage
uctuations/icker
emissions
IEC 6100-3-3
The IPC™ System is intended for use in the electromagnetic environment specied below. The customer or the user of the IPC™ System should assure that it is used in such an
environment.
Immunity test IEC 60601-1-2 test level Compliance level Electromagnetic environment - guidance
Electrostatic
discharge (ESD) IEC
61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
Power frequency
(50/60 Hz)
magnetic eld
IEC 61000-4-8
NOTES:
1. UT is the mains voltage prior to application of the test level.
2. When the console is powered and connected to the footswtich, application of -15KV air discharge onto the footswitch buttons may cause
the console to freeze. Power cycle the console to re-establish normal operation.
Group 1 The IPC™ System uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause
Class A The IPC™ Systems suitable for use in all establishments, ther than domestic and those directly connected to the public low-
Class A
Complies
any interference in nearby electronic equipment.
voltage power supply network that supplies buildings used for domestic purposes.
Guidance and manufacturer’s declaration – electromagnetic immunities - part I
± 8 kV contact
± 15 kV air
± 2 kV for power supply lines
± 1 kV for input/output lines
± 1 kV line to line
± 2 kV line to earth
0% UT (100% dip in UT)
for 0.5 cycle at 0°, 45°, 90°, 135°,
180°, 225°, 270°, and 315°
0% UT (100% dip in UT)
for 1 cycle at 0°
40% UT (60% dip in UT) for
5 cycles
70% UT (30% dip in UT) for 0.5 sec
0% UT (100% dip in UT) for 5 sec
30 A/m 30 A/m Power frequency magnetic elds should be at levels characteristic of a typical location
± 8 kV contact
± 15 kV air
± 2 kV for power supply lines
± 1 kV for input/output lines
± 1 kV line to line
± 2 kV line to earth
0% UT (100% dip in UT)
for 0.5 cycle at 0°, 45°, 90°, 135°,
180°, 225°, 270°, and 315°
0% UT (100% dip in UT)
for 1 cycle at 0°
40% UT (60% dip in UT) for
5 cycles
70% UT (30% dip in UT) for 0.5 sec
0% UT (100% dip in UT) for 5 sec
The relative humidity should be at least 5% Note-1.
Mains power quality should be that of a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital environment.
If the user of the IPC™ System requires continued operation during power mains
interruptions, it is recommended that the IPC™ System be powered from an
uninterruptible power supply or a battery.
in a typical commercial or hospital environment.
Integrated Power Console (IPC™) System
1-13
IPC™ SYSTEM
Guidance and manufacturer’s declaration – electromagnetic immunities - part II
The IPC™ System is intended for use in the electromagnetic environment specied below. The customer or the user of the IPC™ System should assure that it is used in such an
environment.
Immunity test IEC 60601-1-2 test
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is aected by absorption and reection from structures, objects and people.
level
3 Vrms
150 kHz to 80 MHz
6 Vrms
150 kHz to 80 MHz
in ISM bands and
amateur radio bands
3 V/m
80 MHz to 2.7 GHz
9–28 V/m
Spot frequencies
385 MHz–5.785 GHz
Pulse modulation
Compliance level Electromagnetic environment - guidance
3 Vrms
150 kHz to 80 MHz
6 Vrms
150 kHz to 80 MHz
in ISM bands and
amateur radio bands
3 V/m
80 MHz to 2.7 GHz
9–28 V/m
Spot frequencies
385 MHz–5.785 GHz
Pulse modulation
Portable RF communications equipment (including peripherals such as antenna cables and external antennas)
should be used no closer than 30cm (12 inches) to any part of the IPC™ System, including cables specied by
the manufacturer. Othewise, degradation of the performance of this equipment may result.
Portable and mobile RF communications equipment should be used no closer to any part of the IPC™ System
including cables, than the recommended separation distance calculated from the equation applicable to the
frequency of the transmitter.
Recommended separation distance
where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter
manufacturer, E is the immunity test levels in volt per meter (V/m), and d is the recommended separation
distance in meters (m).
Interference may occur in the vicinity of equipment marked with the following symbol:
d = (6/E) √P
Recommended separation distances between
portable and mobile RF communications equipment and the IPC™ System
The IPC™ System is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the IPC™ System can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the IPC™ System as recommended
below, according to the maximum output power of the communications equipment.
Rated
maximum
output
power of
transmitter
P(W)
0.01 0.03 0.03 0.07 0.03 0.03 0.03 0.07
0.1 0.07 0.07 0.21 0.07 0.07 0.07 0.21
1 0.22 0.22 0.67 0.22 0.22 0.22 0.67
10 0.7 0.7 2.12 0.7 0.7 0.7 2.12
100 2.2 2.2 6.7 2.2 2.2 2.2 6.7
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be determined using the equation applicable to the
frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is aected by absorption and reection from structures, objects and people.
380 MHz–390MHz
d = 0.22√P
430 MHz–470MHz
d = 0.22√P
Separation distance according to frequency of transmitter m
704 MHz–787MHz
d = 0.67√P
800 MHz–960MHz
d = 0.22√P
1.7 GHz–1.99GHz
d = 0.22√P
2.4 GHz–2.57GHz
d = 0.22√P
5.1 GHz–5.8GHz
d = 0.67√P
1-14
Integrated Power Console (IPC™) System
IPC™ SYSTEM
Limited warranty
A. This Limited Warranty provides the following assurance for the customer who purchases a Medtronic IPC System. This Limited Warranty is ex-
tended only to the buyer purchasing the IPC System directly from Medtronic or from its aliate or its authorized distributor or representative.
The IPC System includes the console, foot control, and Intelliow remote control (hereinafter referred to as Single Use Components) and jointly
referred to as the IPC System, unless specically noted.
i. Should a System Component fail to function to Medtronic’s published specications during the term of this Limited Warranty (one [1] year
from the date of sale of a new System Component or ninety [90] days from the date of sale of a refurbished or used System Component),
Medtronic will either repair or replace the Motor Component or any portion thereof.
ii. Should a Semi-reusable Component fail to function to Medtronic’s published specications during the term of this Limited Warranty (thirty
[30] days from the date of sale of a new Semi-reusable Component), Medtronic will replace the Semi-reusable Component or any portion
thereof.
iii. Should a Single Use Component fail to function to Medtronic’s published specications prior to its “use by” date Medtronic will replace the
Single Use Component.
B. To qualify for this Limited Warranty, the following conditions must be met:
i. The Product must be used on or before its “Use By” or “Use Before” date, if applicable.
ii. The Product must be used in accordance with its labeling and may not be altered or subjected to misuse, abuse, accident or improper
handling.
iii. Medtronic must be notied in writing within thirty (30) days following discovery of a defect.
iv. The Product must be returned to Medtronic within thirty (30) days of Medtronic receiving notice as provided for in (3) above.
v. Upon examination of the Product by Medtronic, Medtronic shall have determined that: (i) the Product was not repaired or altered by any-
one other than Medtronic or its authorized representative, (ii) the Product was not operated under conditions other than normal use, and
(iii) the prescribed periodic maintenance and services, if applicable, have been performed on the Product.
C. This Limited Warranty is limited to its express terms. THIS LIMITED WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED
WHETHER STATUTORY OR OTHERWISE, INCLUDING ANY IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.
In no event shall Medtronic be liable for any consequential, incidental, prospective or other similar damage resulting from a defect, failure, or
malfunction of the IPC System, whether a claim for such damage is based upon the warranty, contract, negligence or otherwise.
D. The exclusions and limitations set out above are not intended to, and should not be construed so as to, contravene mandatory provisions of
applicable law. Users may benet from statutory warranty rights under legislation governing the sale of consumer goods. If any part or term of
this Limited Warranty is held by any court of competent jurisdiction to be illegal, unenforceable, or in conict with applicable law, the validity
of the remaining portion of the Limited Warranty shall not be aected, and all rights and obligations shall be construed and enforced as if this
Limited Warranty did not contain the particular part or term held to be invalid.
For items contaminated with TSE agents
Medtronic recommends incineration of devices that have directly or indirectly contacted patients suspected or conrmed with prions or a
Transmissible Spongiform Encephalopathy (TSE) such as Crutzfeld-Jakob disease (CJD).
Integrated Power Console (IPC™) System
1-15
TROUBLESHOOTING
Troubleshooting
For any troubleshooting items not corrected by the actions below, contact Customer Service.
General system troubleshooting
Issue Possible Cause Action
Pump(s) does not run. Failed internal components. Contact Customer Service
Little or no irrigation ow. Tubing Set improperly seated in pump. Reposition tubing in pump, verify pump lid
is fully closed with the uid ow from left to
right.
Tubing is pinched or kinked. Check tubing at side of pump, see Irrigation/
Coolant Pumps.
Check remaining tubing for pinched or kinked
areas, if necessary replace tubing.
Tubing clamps are restricting ow. Set tubing clamps in “open” position.
Irrigation ow rate setting low. Adjust irrigation ow rate.
Irrigator obstructed. Replace irrigator.
Pump stall error. Tubing set improperly placed in pump. Reposition tubing in pump, verify pump lid
is fully closed with the uid ow from left to
right.
Tubing is pinched or kinked. Check tubing is not pinched or kinked on side
of pump (see section on “Irrigation/Coolant
Pumps”).
Handpiece connected but console reads
“Connect Handpiece.”
Handpiece connected but console displays
incorrect handpiece.
Console does not power up. Power cord not properly connected. Connect power cord.
Power switch light is on but Touchscreen does
not come on.
Console does not power down. Power switch failure. Unplug power cord, Contact Customer Service.
Touchscreen does not respond. Screen gasket displaced or failed internal
Touchscreen does not work properly. Touchscreen not calibrated. Calibrate Touchscreen.
Console displays wrong handpiece / motor type. Console misidentied the handpiece /
Moisture in cable conicts with handpiece
recognition.
No power. Check power available (i.e. power strip is on,
Power Inlet Fuses blown. Replace fuses with 5.00 A, 250 V, time delayed
Failed internal components. Contact Customer Service.
Failed internal components. Contact Customer Service.
components.
motor.
Run a dry cycle when sterilizing.
circuit breaker is closed, etc.).
fuses (P/N 11270066 Fuse Kit 1898125 ).
Contact Customer Service.
Disconnect and reconnect the motor cable.
Turn console o then on.
1-16
Moisture in cable conicts with handpiece
recognition.
Change motor, motor cable, or console to
isolate the problem.
Run a dry cycle when sterilizing.
Integrated Power Console (IPC™) System
TROUBLESHOOTING
Issue Possible Cause Action
Foot control unit buttons or pedal does not
respond.
Faulty Y-Splitter. Disconnect Y-Splitter and connect FCU to IPC
directly.
Incorrect use. Press and hold buttons for at least 1 second,
wait for console conrmation beep.
Top button does not respond. One (1) handpiece connected (top button has
no function with 1 handpiece connected).
Connector not fully inserted. Disconnect and reconnect the FCU cable
connector.
Try dierent FCU or console to isolate the
problem.
Internal component failure. Contact Customer Service.
Handpiece fails to rotate. Failed foot switch. Disconnect foot switch, use manual start/stop
rocker switch on rear of console.
Failed handpiece motor or motor driver. Contact Customer Service.
Cables are not property connected. Ensure handpiece cable is properly connected.
Cables are damaged. Check cables for cracks, splits, or bent
connector pins.
Handpiece is too hot to touch/hold. Blade, bur, and/or attachment transferring
heat to handpiece.
Remove and reinstall or change blade, bur,
and/or attachment. Ensure the part is properly
seated before resuming use.
Inadequate irrigation and/or coolant. Ensure adequate irrigation and/or coolant is
present.
Integrated Power Console (IPC™) System
1-17
ERROR CODES
Error codes
Code # Title Cause Description
1 MCB does not report that it booted within 5 seconds of AI telling it
to start and subsequent reattempts fail.
2 NOT USED. NOT USED. NOT USED
3 UI-MCB Com Failure - Max resends exceeded. System Error. Power o. Wait 10 seconds. Power on. If
4 UI-MCB Com Failure - Get answer failed.
5 UI-MCB Com Failure - No status message received.
6 UI-MCB Com Failure - Serialization ID error.
7 UI-MCB Com Failure - Timeout exception.
8 UI-MCB Com Failure - Variable not recognized.
9 Pump 1 stalled (no transitions on opto sensor). Pump #1
10 Pump 2 stalled (no transitions on opto sensor). Pump #2
11 Unrecognized/damaged handpiece plugged in on port 1 (rst 12
pin).
12 Unrecognized/damaged handpiece plugged in on port 2 (second
12 pin).
13 Unrecognized/damaged handpiece plugged in on port 3 (4 pin).
14 Unrecognized/damaged handpiece plugged in on port 4 (Skeeter).
15 Handpiece stalled. Handpiece
16 MCB motor overcurrent detected. Motor
17 Unrecognized/damaged multifunction foot pedal plugged in. Foot Pedal
System Error. Power o. Wait 10 seconds. Power on. If
error persists, call Customer Service.
error persists, call Customer Service.
Check tubing connection.
stalled.
Check tubing connection.
stalled.
Handpiece. Unplug handpiece and plug back in. If error
persists, replace handpiece.
Check accessory.
stalled.
Unplug handpiece and plug back in. If error
overcurrent.
persists, replace handpiece.
When using foot pedal only, unplug foot
Connection
error.
pedal and plug back in. If error persists,
replace foot pedal or switch to manual
control.
When using Y-Splitter, disconnect foot pedal
and Y-Splitter, then connect foot pedal
directly to IPC™. If after reconnecting foot
pedal, the error goes away, replace Y-Splitter
with another unit. If error persists, replace
foot pedal and reconnect both Y-Splitter
and foot pedal or switch to manual control.
18 Damaged handpiece or nger lever base out of position. Finger Control
error.
Stylus Touch™ - A nger control error has
been detected. Check that the control lever
ring is properly seated in one of the four
possible positions. If error persists contact
Customer Service. Press OK to use alternate
control method.
POWEREASE™ - Please check mode select
switch to ensure a mode has been selected
by rotating mechanism until it rests in a
detent. If error persists, contact Customer
Service.
19 UI self test failure - culture (language) registry entry. Self Test Failed. Power o. Wait 10 seconds. Power on. If
20 UI self test failure - sector conguration registry entry.
error persists, call Customer Service.
21 UI self test failure - corrupt usage data le or unable to create usage
data le.
22 NOT USED. NOT USED. NOT USED.
1-18
Integrated Power Console (IPC™) System
ERROR CODES
Code # Title Cause Description
23 MCB non-specic self test failure. Self Test Failed. Power o. Wait 10 seconds. Power on. If
24 MCB self test failure - port 1.
error persists, call Customer Service.
25 MCB self test failure - port 2.
26 MCB self test failure - port 3.
27 MCB self test failure - port 4.
28 MCB self test failure - bridge transitor 1 shorted.
29 MCB self test failure - bridge transitor 2 shorted.
30 MCB self test failure - bridge transitor 3 shorted.
31 MCB self test failure - bridge transitor 4 shorted.
32 MCB self test failure - bridge transitor 5 shorted.
33 MCB self test failure - bridge transitor 6 shorted.
34 MCB self test failure - A/D converter.
35 MCB self test failure - motor error.
36 MCB self test failure - 3.3 volt supply.
37 MCB self test failure - 12 volt supply.
38 MCB self test failure - 48 volt supply.
39 MCB self test failure - FCU port.
Integrated Power Console (IPC™) System
1-19
CLEANING AND STERILIZATION
Cleaning and sterilization
Reprocessing Instructions are subject to change. Refer to manuals.medtronic.com for current Reprocessing Instructions.
Clean the multifunction foot pedal
• If debris is present under the foot pedal’s boot, return for warranty service.
• Do not immerse or sterilize the foot pedal.
• Do not use alcohol, other solvents or abrasive cleaners.
1. On the slip resistant foot pad ONLY, spray a neutral enzymatic detergent, pH 6.0-8.0, or a phenol based disinfectant, mixed according to
manufacturer’s instructions.
2. Leave the solution on the foot pad for approximately 10 minutes.
3. Dampen a cloth with a neutral enzymatic detergent, pH 6.0-8.0, or a phenol based disinfectant, mixed according to manufacturer’s
instructions.
4. Wipe the foot pedal with the damp cloth until visually clean.
5. Dry the unit with a clean, non-abrasive cloth.
Clean the Y-Splitter
1. Do not immerse or sterilize the Y-Splitter.
2. Do not use alcohol, other solvents or abrasive cleaners.
3. Dampen a cloth with a neutral enzymatic detergent, pH 6.0 – 8.0, or a phenol based disinfectant, mixed according to manufacturer’s
instructions.
4. Wipe the Y-Splitter with a damp cloth until visually clean.
5. Dry the unit with a clean, non abrasive cloth.
1-20
Integrated Power Console (IPC™) System
Customer service
For further information regarding the use of this product or to report any problems, please contact Medtronic using the appropriate information
provided on the blue and white contact information card packaged with each device; or contact your local distributor.
Medtronic Powered Surgical Solutions
4620 North Beach Street
Fort Worth, Texas 76137 USA
www.medtronic.com
US Help Line
800 468 9710
International Service
International Customers should contact their local Medtronic Neurologic Technologies representative.
The following are trademarks or registered trademarks of Medtronic, Inc. in the United States and other countries: Intelliow™, IPC™, Legend EHS™, Midas Rex™,
Stylus Touch™. All other trademarks, service marks, registered trademarks or registered service marks are the property of their respective owners in the United States
and other countries.
The information contained in this document is accurate at time of publication. Medtronic reserves the right to make changes to the product described in this manual.
Refer to manuals.medtronic.com for the current version.
Medtronic Xomed
6743 Southpoint Drive North
Jacksonville, Florida 32216-0980
USA
medtronic.com
+1 800 874 5797
EC REP
Authorized Representative in the European Community
Medtronic B.V.
Earl Bakkenstraat 10
6422 PJ Heerlen
The Netherlands
+31 45 566 8000
Europe/Middle East/Africa
Medtronic International Trading Sàrl
Route du Molliau 31
Case Postale 84
CH- 1131 Tolochenaz
Switzerland
+41 21 802 7000
Australia
Medtronic Australasia Pty Ltd
2 Alma Road
Macquarie Park, NSW 2113
Australia
Canada
Medtronic of Canada Ltd
99 Hereford Street
Brampton, Ontario L6Y 0R3
Canada
+1 905 460 3800
Technical manuals
medtronic.com/manuals
© 2019 Medtronic
175027EN
M988671A001 A
2019-05
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