MTP 3000 User manual

MODEL 3000
PHACOEMULSIFICATION SYSTEM
Operator’s Manual

TO OUR VALUED CUSTOMERS:
Thank you for purchasing the Model 3000 Phacoemulsification System (Model 3000)
by Medical Technical Products, LP (MTP). The Model 3000 is intended for use in the
disruption and extraction of cataractous lens material from the eye with the use of
ultrasonic energy, a process known as “Phacoemulsification”.
The Model 3000 is both 510(k) cleared1and CE Marked2. The Model 3000 is the latest
example of our commitment to provide products that meet customer expectations of
quality, performance, and value.
The operator’s manual is your written guide to the Model 3000. Please read the entire
manual carefully. DO NOT attempt to use the system without having an adequate
understanding of all of its functions, controls, and limitations.
No information on surgical procedures is given in this manual. MTP claims no
responsibility or liability resulting from any technique practiced.
Pay close attention to warnings and cautions throughout this manual.
If you have any questions or require additional information, please contact Medical
Technical Products, LP Customer Service at:
1022 Fuller Street
Santa Ana, CA 92630
Tel: [phone]
www.medtechprods.com
Monday – Friday 9:00 AM to 5:00 PM (PST)
1 510(k) No. K080803, dated 09/22/08

Model 3000 PHACOEMULSIFICATION SYSTEM
Model 3000 PHACO PACKAGE
Qty
Part Number
Description
1
551-0034-001
Console, MTP
1
553-0001-001
Footpedal, Model 3000
1
01-899145
US Handpiece, STT
1
551-7002-001
Travel Case
1
23-9024
US Tip Pack, 19 GA, 30°, LT
1
551-0067-001
Collection Bags, 10 pk
1
551-0050-001
Tubing Cartridge
1
17031-S2-8
Power Cord, 120V (USA)
1
551-7001-001
Vinyl Cover
1
551-6001-001
Operator’s Manual
1
430-2215-002
Fuse Set
SYSTEM COMPONENTS SOLD SEPARATELY
Part Number
Description
551-0052-001
Automated IV Pole Cart
553-0001-001
Footpedal, Model 3000
01-899145
US Handpiece, STT
01-899530
US Handpiece, Mini
551-7002-001
Travel Case
430-2215-002
Fuse Set
17031-S2-8
Power Cord, 120V (USA)
551-7001-001
Vinyl Cover
551-6001-001
Operator’s Manual
TUBING CARTRIDGE & ACCESSORIES
Part Number
Description
551-0102-004
Tubing Set (4 Tubing Cartridges & 40 Collection Bags)
551-0067-001
Collection Bags (pack of 10)
US PHACO TIPS & ACCESSORIES
Part Number
Description
23-9024 US Tip Pack (Qty 1 ea: US Tip, 30°, 19 GA; US Tip Wrench;
Irrigation Sleeve; Test Chamber)
23-9022
US Tip, 30°, 20 GA
23-9023
US Tip, 30°, 19 GA
23-9020
US Tip Wrench
23-9003
19 GA Irrigation Sleeve
23-9021
20 GA Irrigation Sleeve
23-9004
Test Chamber (Pack 5)
IA HANDPIECES & ACCESSORIES
Part Number
Description
23-9000
IA Handpiece, Titanium
23-9001
Aspiration Tip (0.3 mm)
23-9002
Aspiration Tip (0.3 mm, 45°)
23-9003
19 GA Irrigation Sleeve (Pack5)
VITRECTOMY
Part Number
Description
23-9006
Vitrector, Guillotine (includes Irrigation Sleeve)
CAUTERY
Part Number
Description
23-9050
Forceps, Straight (0.4 mm)
23-9051
Cord, Cautery, Reusable 12’

Page 1 of 90
TABLE OF CONTENTS
1.0 WARNINGS AND PRECAUTIONS .………………………………………………………4
2.0 WARRANTY INFORMATION .……………………………………………………………..6
3.0 PRODUCT INFORMATION .……………………………………………………………….7
3.1 UNPACKING THE SYSTEM .…………….………………….………………….………………….…………………... 7
3.2 OPERATOR’S MANUAL .……………….………………….………………….………………….…………………….. 7
3.3 SYSTEM CONSOLE .………………….………………….………………….………………….………………………. 7
3.4 SYSTEM HANDPIECE .……………….………………….………………….………………….……………………..... 8
3.5 SYSTEM TUBING CASSETTE .……………….………………………….………………….……………………....... 8
3.6 SYSTEM FOOT PEDAL .……………………….………………………….………………….……………………....... 8
3.7 (OPTIONAL) CARTWITH IV POLE .……………….………………………….………………….……………......... 9
4.0 SYSTEM DESCRIPTION .………………………………………………………………...10
4.1 SYSTEM OVERVIEW .………………….………………….………………….………………….…………………… 10
4.2 SYSTEM SIGNS AND SYMBOLS .……………………….……………….………………….…………………….... 16
4.3 TECHNICAL SPECIFICATIONS .………………….……………………….………………….……………………... 18
4.4 ENVIRONMENTAL REQUIREMENTS .………………….……………….………………….………………………. 21
4.5 FACTORY DEFAULT SETTINGS .………………….……………….….………………….………………………. 21
5.0 SYSTEM OPERATION OVERVIEW .………………………………………………........22
5.1 SYSTEM SOFTWARE OVERVIEW .……………………………………………………….……….……………….. 22
5.2 MAIN MENU .………….…………………….………………….………………….………………….……………….. 24
5.3 IRRIGATION (IRR) MODE .………….……………………….………………….………………….……………….. 26
5.4 PHACO (U/S) MODE …………….…………………….………………….………………………….……………… 28
5.4.1 Phaco Mode Functions.………….…………………….………………….………………….………………... 29
5.4.2 Phaco Normal Mode.……………….…………………….………………….………………….……………… 30
5.4.3 Phaco Burst Mode.……………….…………………….………………….………………….……………….. 32
5.4.4 Phaco Micro Mode.……………….…………………….………………….………………….……………….. 33
5.4.5 Multimode Soft-keys 1, 2, 3.…………………….………….………………….………………….…………... 35
5.5 IRRIGATION /ASPIRATION (I/A) MODE ..…………….…………………….…………………….……………… 36
5.5.1 I/A Mode Functions.……………….…………………….………………….………………….……………….. 37
5.5.2 Multimode Soft-keys I/A1, I/A2, and Cap Vac .….…………………….………………………….……….. 38
5.6 VITRECTOMY (VIT) MODE .….……………………….…………………….…………………….………………... 39
5.6.1 VIT Mode Functions .………….……………….……….…………………….………………………….……… 40

Page 2 of 90
TABLE OF CONTENTS (continued)
5.7 COAGULATION (COAG) MODE .…………………….…………………….…………………….………………... 41
5.8 HELP MODE .……………………………………….….….…………………….…………………….……………….. 42
5.9 OPTIONS MODE .……………………………………….….….……………….…………………….……………….. 43
5.9.1 PROGRAMS Mode .……………….……………………………………….………………….……………….. 43
5.9.2 Create and Save a Custom Program.……………….…………………….……………….………………. 44
5.9.3 Recalling a Program.……………….…………………….………………….………………….……………… 45
5.9.4 Renaming a Saved Program without Changing Program Settings.………………………………….. 45
5.9.5 Change Saved Program Settings without Changing the Program Name..........................................46
5.9.6 Delete Program Names.…………………………………….…………….………………….……………….... 46
5.9.7 SETTINGS Mode.........................................................................................................................................47
5.9.8 Sound............................................................................................................................................................47
5.9.9 Change an Audible Indicator Setting.......................................................................................................48
5.9.10 Voice.............................................................................................................................................................49
5.9.11 Change Voice Indicator Setting................................................................................................................50
5.9.12 Video.............................................................................................................................................................51
5.9.13 Change Video Brightness Setting............................................................................................................51
5.9.14 Preferences..................................................................................................................................................52
5.9.15 Change Preference Settings.....................................................................................................................53
5.9.16 FOOTPEDAL Mode....................................................................................................................................54
5.9.17 FOOT PEDAL CALIBRATION PROCEDURE ......................................................................................56
6.0 SYSTEM SETUP AND PREOPERATIONAL CHECKS .………………………...........58
6.1 SYSTEM SETUP .………………………………………………………………………………………………………. 58
6.2 ACCESSORY SETUP .……………………………………………………………….………………………………... 60
6.2.1 Irrigation / Aspiration Handpiece .…………………………………………………………………………….. 60
6.2.2 Vitrectomy Handpiece .………………………………………………………………………………………….. 61
6.2.3 Cautery Handpiece ..…………………………………………………………………………………………….. 61
6.2.4 Ultrasonic Handpiece .…………………………………………………………………………………………... 62
6.3 SYSTEM PREOPERATIONAL CHECKS .………………………….………………….………….………………… 64
6.3.1 Prime Cycle .………………………………………………………………………………………………………. 64
6.3.2 System Fluidics Test .…………………………………………………………………………………………… 64

Page 3 of 90
TABLE OF CONTENTS (continued)
7.0 SYSTEM OPERATION .…………………………………………………………..…........65
7.1 IRR MODE .……………………………………………………………………………………………………………. 65
7.2 U/S PHACO MODE .…………………………………………………………………………………………………. 66
7.3 I/AMODE ..…………………………………………………………………………………………………………….. 67
7.4 VIT MODE .……………………………………………………………………………………………………………. 68
7.5 COAG MODE .……………………………………………………………………………………………………….. 69
7.6 REPLACING THE IRRIGATION SOLUTION CONTAINER..…………………………………………………….. 70
7.7 REPLACING THE ULTRASONIC (U/S) HANDPIECE.………………………………………………………….. 71
7.8 SYSTEM MESSAGES .………………………………………………………………………………………………. 72
8.0 SYSTEM CLEANING.................................................................................................74
8.1 PURGING THE SYSTEM CONSOLE ..…………………………………………………………………………….. 74
8.2 CLEANING THE SYSTEM CONSOLE .……………………………………………………………………………. 75
8.3 CLEANING THE FOOT PEDAL.……………………………………………………………………………………. 75
8.4 CLEANING THE OPTIONAL CARTWITH IV POLE ...………………………………………………………….. 76
8.5 CLEANING ACCESSORIES .……………………………………………………………………………………….. 76
8.6 CLEANING VITRECTOR .………………………………………………………………………………………….... 77
8.7 STERILIZATION ..…………………………………………………………………………………………………….. 77
9.0 SYSTEM SERVICE....................................................................................................78
9.1 FUSE REPLACEMENT .…………………………………………………………………………………………….. 78
9.2 CONTACT TECHNICAL SUPPORT ...…………………………………………………………………………….. 79
10.0 SYSTEM TROUBLESHOOTING.............................................................................. 80
11.0 SYSTEM PERFORMANCE ...................................................................................... 85
11.1 EMC REQUIREMENTS FOR THE MODEL PHACOEMULSIFICATION SYSTEM.……………………….. 86

Page 4 of 90
1.0 WARNINGS AND PRECAUTIONS
DANGER: Possible risk of fire or explosion! The Model 3000 Phacoemulsification System (Model
3000) should never be used in the presences of flammable anesthetics, oxidizing gases (i.e. nitrous
oxide, oxygen), endogenous gases, disinfecting agents, cleaning agents, or aerosol sprays.
WARNING: Inspect condition of all operating equipment prior to beginning surgical procedure.
WARNING: Failure of the system could result in an unintended increase of output power.
WARNING: The patient should not come into contact with metal parts which are earthed or which
have an appreciable capacitance to earth (for example, operating table supports, etc.).
WARNING: Skin-to-skin contact (e.g. between the arms and body of the patient) should be avoided,
e.g. by insertion of dry gauze.
WARNING: Electrical shock hazard exists. DO NOT remove console cover. Call manufacturer for
service.
WARNING: Pinch point hazard exists. Keep hands and fingers clear when lowering the display.
WARNING: Console rear panel network and USB connections are for use by trained factory
personnel only.
WARNING: To avoid the risk of electric shock, this equipment must only be connected to a supply
mains with protective earth.
WARNING: The console can only be disconnected from the supply mains by means of the power
cord. Position the equipment so that the power cord is easily accessible.
WARNING: No modification of this equipment is allowed.
WARNING: The use of accessories other than those listed in this manual has not been evaluated
for safety and performance.
WARNING: The following components must be sterilized prior to their use: Ultrasonic Handpiece,
Tubing Set, Phaco Tip and Wrench, silicone Tip Sleeve, and Test Chamber. Consult package labels
and instructions that accompany these components for reprocessing instructions.
WARNING: Only use ultrasonic handpieces listed in this manual.
WARNING: Do not activate the “prime” and / or “tune” functions while handpiece is in the eye, as
this can create a hazardous situation that could result in patient injury.
WARNING: Connected accessories should be rated for at least the minimum peak output voltage
of the Model 3000 set at the intended output control setting in the intended operating mode.
WARNING: Avoid HF output settings where maximum output voltage may exceed rated accessory
voltage.
WARNING: Surgical waste presents a biological hazard and must be handled and disposed of
according to local governing ordinances.
WARNING: Follow local governing ordinances and recycling plans regarding disposal or
recycling of device components, accessories and packaging.
WARNING: The ultrasonic handpiece and foot pedal must be disposed of according to local
regulations at the end of their useful lives.
WARNING: Use of a damaged U/S tip or one that has been used excessively may adversely affect
healthy tissue.
WARNING: Never use a damaged or intentionally modified U/S tip as they could break or
malfunction.

Page 5 of 90
WARNING: Do not check function of ultrasonic handpiece by placing hand or finger against tip or
unintended damage to healthy tissue may result.
WARNING: Ensure sufficient volume of irrigation solution for the procedure. Level should be
monitored during the procedure.
WARNING: Ensure that the maximum capacity of the collection bag is not exceeded as this could
cause a hazardous situation to the patient.
WARNING: Do not manually force the pole height because this could cause incorrect indication of
bottle height and patient injury.
WARNING: Intraocular pressure of the eye can be affected by the suspension height of the
irrigating solution and vacuum level during surgery. Irrigation solution source must be at or above
the patient’s eye level.
WARNING: Use only tubing set approved for Model 3000.
WARNING: The level of the patient’s eye must be between the bottom of the installed tubing
cassette and no more than ten (10) centimeters below the bottom of the installed tubing cassette to
ensure proper fluid dynamics of the vacuum system.
WARNING: Hazards may exist with patients with cardiac pacemakers or other active implants due
to frequency interference with the action of the pacemaker or damage to the pacemaker itself.
WARNING: Ensure that any other monitoring electrode equipment or electromagnetic equipment
near the patient will not interfere with the surgical procedure or place the patient at risk with undue
contact when used simultaneously with the Model 3000 Phacoemulsification System.
WARNING: Interference produced by operation of the Model 3000 Phacoemulsification System may
adversely influence the operation of other electronic equipment.
WARNING: Electrode cables should be positioned in such a way that contact with the patient or
other cables is avoided.
WARNING: Temporarily unused active electrodes should be stored in a location that is isolated from
the patient.
WARNING: The output power selected should be as low as possible for the intended purpose.
WARNING: To reduce the risk of accidental burns, caution should always be taken when operating
high frequency surgical equipment.
CAUTION: Do not activate the ultrasonic handpiece with the tip in air as immediate, irreparable
damage may result.
CAUTION: Do not use abrasive cleaners or solvents on the system console, particularly the
touchscreen. Non-flammable agents should be used for cleaning and disinfection wherever possible.
CAUTION: Do not spray liquids directly onto the system console or submerge the system console or
foot pedal into liquids – see Chapter 9 Cleaning.
CAUTION: Do not activate the US Handpiece continuously at 100% power for more than 1 minute,
50% duty cycle.

Page 6 of 90
WARRANTY
2.0 WARRANTY INFORMATION:
The Model 3000 Phacoemulsification System (Model 3000) is intended for use by
medically-trained / qualified ophthalmic / cataract surgeons who bear full responsibility for
safe use at all times. Further, to repeat Medical Technical Products LP (MTP) earlier
instruction (Section 1.0 Warnings and Precautions), the operator must read this manual
carefully and become familiar with all its warnings.
MTP makes no medical recommendation. Use of the Model 3000 is a matter of
professional medical judgment in all cases.
MTP shall not, in any event, be liable for any actual or anticipated injury, direct, indirect,
special, incidental, or consequential damages arising out of the use of this product,
even if advised of the possibility of damage. Specifically, MTP is not liable for any costs,
such as lost profits or revenue, loss of MTP product use, substitute costs, third party
claims, or otherwise. Further, MTP’s sole liability is limited to the amount equal to the
purchased product price subsequent to any claim. This liability may not be waived or
amended without express written consent by MTP.
MTP warrants its products to be free from defects in materials and workmanship for a
period of one (1) year from the purchase date. This warranty does not apply to
products which have been damaged by accident, abuse, modification, misapplication,
and / or resulted from an unsuccessful attempted remedy of any confirmed /
unconfirmed nonconformance by a non-MTP trained field service technician/engineer.
This warranty applies only to the original purchaser and is not transferrable. Warranty
on consumable products is limited to the first use.
MTP’s sole warranty obligation under this warranty is limited to repairing / servicing or
replacing, at its option, any defective product. This limited warranty is exclusive and shall
be in lieu of all other expressed warranties, whether written, verbal, or implied, including
any warranty of fitness for a particular purpose or merchantability. The purchaser waives
all other warranties, guarantees, or liabilities arising by law or otherwise.

Page 7 of 90
SYSTEM INFORMATION
3.0 PRODUCT INFORMATION
3.1 UNPACKING THE SYSTEM
Your Model 3000 Phacoemulsification System (Model 3000) was thoroughly inspected and
tested prior to shipment. Carefully unpack and visually inspect all items for any apparent
damage that may have occurred during shipment. If any physical damage is found or any
item is missing when received, immediately notify the shipping company and Medical
Technical Products, LP (MTP). All claims for damage should be filed promptly.
NOTE: All packaging material should be saved for repackaging and returning the
system if necessary.
3.2 OPERATOR’S MANUAL
The Operator’s Manual for the Model 3000 provides the necessary system information for
the following areas:
System Description
System Setup and Preoperational Checks
System Operation Overview
System Operation
System Cleaning and Storage
System Service
System Troubleshooting
System Cleaning and Storage
WARNING: DO NOT attempt to setup and/or operate the Model 3000 until you have read
and understood the entire contents of the Operator’s Manual. You must have the knowledge
and a good understanding of the operational functions, controls, and limitations of the system
before its use.
Information on surgical procedures is not provided in this manual. MTP is not
responsible nor liable for malpractice resulting from any surgical techniques practiced.
3.3 SYSTEM CONSOLE
The Model 3000 utilizes a versatile, advanced microprocessor for control of all primary
functions. It operates with time-saving simplicity and it is extremely easy to operate.
The system requires no external air source and accepts a voltage range from 100 to 240
VAC. All operational functions, modes, and program options are independently set by
utilizing the system operational menus on the touchscreen of the console.
The tubing cassette loading process is simplified by a latch mechanism on the side of the
console which allows the operator to place and lock the cassette with ease.

Page 8 of 90
3.4 SYSTEM HANDPIECE
The Model 3000 features an Ultrasonic (U/S) Handpiece that receives an electrical energy
signal from the attached console and transfers it into a mechanical motion. This is
accomplished through the use of piezoelectric crystals, which are located inside an
environmentally isolated chamber at the interior of the handpiece. The mechanical motion, with
a frequency around 40 kHz and amplitude of a few thousandths of an inch, is then transferred
to an attached tip. The tip is inserted into the eye by the surgeon and placed in contact with the
intraocular lens. The vibrating motion of the tip, enhanced by cavitational energy, emulsifies the
lens. The emulsified lens is then aspirated from the eye.
3.5 SYSTEM TUBING CASSETTE
The Tubing Cassette is a reusable component of the Model 3000 that joins the fluid tubing to the
system console without direct fluid contact. The cassette provides connections between an
irrigating fluid source, such as intravenous administration tubing set, the ultrasonic handpiece,
and a waste collection bag. The cassette tubing mates with a pump head in the system console,
which provides the driving force to aspirate the emulsified lens and fluid from the surgical site. A
valve in the system console controls the gravity flow of the irrigating fluid to the surgical site,
maintaining intraocular pressure. The reusable tubing is dual lumen, or two tubes: one to deliver
the irrigating fluid, the other to remove the aspirated material.
3.6 SYSTEM FOOT PEDAL
The operation of the Model 3000 is mainly controlled by the Foot Pedal, which is linked to
the system by a cable connected to the back panel of the system console.
The main foot pedal has three (3) positions of operation:
Position 1: activates Irrigation
Position 2: activates Aspiration along with Irrigation
Position 3: activates the Ultrasonic Power along with Irrigation and Aspiration
NOTE: Foot pedal positions will vary depending on the Operation Mode selected.

Page 9 of 90
3.7 (OPTIONAL) CART WITH IV POLE
The Model 3000 has an Optional Cart with an Automated IV Pole that can be purchased
separately or along with your initial order. The optional cart contains the following features:
Locking casters
Shelf for holding the system console
Hanger for foot pedal storage when not in use
Surgical accessories tray
Automated IV pole
The automated IV pole has two (2) hangers on the top arms of the pole that can suspend one
solution bottle on each hanger. When the cart is connected to the back panel of the console,
the height of the IV pole is controlled from the console touchscreen.
All of the system components will be described in full detail in Section 4.0 System Description of
this manual.

Page 10 of 90
4.0 SYSTEM DESCRIPTION
4.1 SYSTEM OVERVIEW
FIGURES 4-1 through 4-7 refer to all controls, indicators and connections on the Model 3000.
Their associated descriptions are as follows:
Item
#
Name Description
1 REAR PANEL LABEL DISPLAYS SYSTEM RATINGS, SERIAL NUMBER,
ALL WARNINGS AND CAUTIONS
2 ON / OFF SWITCH I (ON) ; O (OFF)
3 RJ 45 CONNECTOR FACTORY USE
4 USB PORTS 1 & 2 FACTORY USE
5 FOOTPEDAL CONNECTOR CONNECTION FOR THE SYSTEM FOOT PEDAL
6 IV POLE CONNECTOR CONNECTION FOR THE OPTIONAL CART WITH
AUTOMATED IV POLE
7 AC POWER INPUT PROVIDES POWER CONNECTION AND
OVERLOAD PROTECTION TO THE SYSTEM
8 FUSE HOLDER CONTAINS TWO SYSTEM FUSES
9 CASSETTE LOCK LOCKING MECHANISM FOR THE TUBING
CASSETTE
10 VENT VALVE CONTROLS ASPIRATION LINE VENTING
11 IRRIGATION VALVE CONTROLS FLOW OF IRRIGATION FLUID
12 CASSETTE RELEASE BUTTON RELEASES THE CASSETTE WHEN PRESSED
13 ULTRASONIC CONNECTOR PROVIDES POWER TO THE ULTRASONIC
HANDPIECE
14 COAGULATION CONNECTOR PROVIDES POWER TO THE CAUTERY
FORCEPS
15 VITRECTOMY PORT PROVIDES AIR TO THE VITRECTOR
16 PERISTALTIC PUMP HEAD PROVIDES FLOW FOR SYSTEM ASPIRATION
17 VACUUM SENSOR SENSOR FOR MEASURING VACUUM
18 TOUCHSCREEN DISPLAY PROVIDES ACCESS TO USER INTERFACE
19 FRONT PANEL PROVIDES DISPLAY FOR THE SYSTEM
OPERATION
20 SPEAKERS PROVIDES AUDIBLE VOICE, INDICATORS AND
ALERTS

Page 11 of 90
4.1 SYSTEM OVERVIEW (CONTINUED)
FIGURES 4-1 through 4-7 refer to all controls, indicators and connections on the Model 3000.
Their associated descriptions are as follows:
Item
#
Name Description
21 CASSETTE ADMINISTRATION TUBE PROVIDES IRRIGATION INPUT FOR TUBING
CASSETE
22 TUBING CASSETTE PROVIDES SYSTEM CONNECTION FOR
IRRIGATION AND ASPIRATION FUNCTIONS
23 COLLECTION TUBE PROVIDES WASTE OUTPUT TO COLLECTION
BAG
24 COLLECTION BAG HANGER HANGER FOR THE COLLECTION BAG
25 IRRIGATION TUBE PROVIDES IRRIGATION INPUT FOR
ULTRASONIC HANDPIECE
26 ASPIRATION TUBE PROVIDES ASPIRATION OUTPUT FOR
ULTRASONIC HANDPPIECE
27 HEEL REST PROVIDES STABLE SURFACE FOR LEVERAGE
ONTO TREADLE
28 MAIN TREADLE ACTIVATES THE BASIC MODES OF THE
SYSTEM, USER INTERFACE FOR CONTROLS
29 LEFT SWITCH (SIDE KICK) ACTIVATES ASSIGNED FUNCTIONS (DEFAULT:
NOT USED)
30 RIGHT SWITCH (SIDE KICK) ACTIVATES ASSIGNED FUNCTIONS (DEFAULT:
REFLUX)
31 ASPIRATION PORT PROVIDES CONNECTION FOR ASPIRATION OF
WASTE
32 IRRIGATION PORT PROVIDES CONNECTION FOR IRRIGATION
FLUID
33 U/S HANDPIECE SOLID TITANIUM CONSTRUCTION.
COMPATIBLE WITH MTP PHACO(S).
34 HANDPIECE ELECTRICAL CONNECTOR PROVIDES POWER TO THE ULTRASONIC
HANDPIECE
35 SOLUTION HANGER HANGER FOR SUSPENDING SOLUTION BOTTLE
36 HANDLE HAND GRIP FOR MOVING THE CART
37 SHELF PROVIDES SECURE MOUNTING LOCATION FOR
SYSTEM CONSOLOE
38 CABLE MANAGEMENT STORES THE WRAPPED POWER CORD WHEN
NOT IN USE
39 FOOT PEDAL HANGER STORES THE FOOT PEDAL WHEN NOT IN USE
40 ACCESSORY TRAY PROVIDES CONVENIENT LOCATION FOR
HANDPIECES AND ACCESSORIES

Page 12 of 90
Figure 4-1: Console Back Panel
Figure 4-2: Connections Side View
1
2
3
4
8
7
6
5
9
10
11
12
13
15
14
16
17
9

Page 13 of 90
Figure 4-3: Console Front View
Figure 4-4: Cassette with Tubing Connection Side View
18
19
20
21
22
24
23
26
25

Page 14 of 90
Figure 4-5: Foot Pedal
Figure 4-6: Phaco Ultrasonic Handpiece and Cable/Connector
29
27
30
28
31
32
33
34

Page 15 of 90
Figure 4-7: Optional Cart with Automated IV Pole
37
40
39
38
36
35

Page 16 of 90
4.2 SYSTEM SIGNS AND SYMBOLS
SIGN / SYMBOL DESCRIPTION SIGN / SYMBOL DESCRIPTION
Alert: Read all related
information. DO NOT bypass.
Humidity Range: Range of
humidity in which the device can
safely and effectively operate.
B - Type Equipment: Providing
a particular degree of protection
against electrical shock,
particularly regarding allowable
leakage currents and reliability of
the protected earth connection (if
present).
Manufacture Date: Year the
device was manufactured.
BF - Type Equipment: As type
(B) but with isolated or floating
(F-type) applied part or parts.
Non-ionizing Radiation: Device
emits electromagnetic radiation
with insufficient photon energy to
ionize matter.
CE Marking Authorization:
Device meets the requirements
of applicable European
Directives.
Not for General Waste:
Component must be properly
disposed of.
Consult Accompanying
Documents.
Pressure Range: Range of
pressure under which the device
can safely and effectively
operate.
Electrical Hazard: Electrical
shock may occur when
performing necessary tasks
associated with electrical
environments.
Serial Number: Identification
number for the system console.
European Authorized
Representative: A legal entity
designated by non- European
Union (EU) manufacturers, to
represent them in the EU and
ensure their compliance with the
European Directives.
Temperature Range: Range of
temperature in which the device
can safely and effectively
operate.
Fuse: Protects the device from
excess electrical current. COAG Coagulation: Power connection
for coagulation handpiece.

Page 17 of 90
4.2 SYSTEM SIGNS AND SYMBOLS (CONTINUED)
SIGN / SYMBOL DESCRIPTION SIGN / SYMBOL DESCRIPTION
I/V POLE I/V Pole: Connection port for the
system (optional) Cart with I/V
Pole. VITVitrectomy: Power connection
for vitrectomy handpiece.
FOOTPEDAL Foot Pedal: Connection port for
the system foot pedal.
System Power ON: When
system is connected to main
power
U/S Ultrasonic: Power connection
for ultrasonic handpiece.
System Power OFF: When
system is disconnected from the
main power
Catalog Number: To identify the
manufacturer’s catalog number.
The catalog number shall be
placed adjacent to the symbol.
Batch Code: To identify the
manufacturer’s batch or lot code.
The code shall be placed
adjacent to the symbol.
Refer to Operator’s Manual:
Operator’s manual must be read.