Pelton & Crane Centennial RD36 Owner's manual

Centennial
Rear Delivery Center
Use & Care
POWER
AUX.
1
AUX.
2
MODE
TIMER
The
Centennial
P
OWE
R
A
U
X.
1
A
U
X.
2
MODE
T
IME
R
The
Centennial
Models: RD42,
RD42C & RD42B (Shown
with Model 2222
Instrument Delivery System
& Model 2238
Assistant’s Instrumentation)
Models: RD36,
RD36C & RD36B
(Shown with Model 2222
Instrument Delivery System
& Model 2238
Assistant’s Instrumentation)

TABLE OF CONTENTS
GENERAL INFORMATION................................................................................................................................................. 3
SAFETY.............................................................................................................................................................................. 4
CENTENNIAL REAR DELIVERY OVERVIEW................................................................................................................... 5
OPERATION....................................................................................................................................................................... 6
CABINETRY FUNCTIONS ................................................................................................................................................. 9
CONTROL PANEL FUNCTION ......................................................................................................................................... 10
ASEPTIC VACUUM OPERATION......................................................................................................................................11
CLEANING, DISINFECTING & STERILIZATION.............................................................................................................. 12
CLEAN WATER SYSTEM ................................................................................................................................................. 13
CARE OF THE UNIT......................................................................................................................................................... 14
ASSISTANT’S VACUUM INSTRUMENTS ........................................................................................................................ 15
CLEANING CABINETRY SURFACES .............................................................................................................................. 16
ADJUSTMENTS................................................................................................................................................................ 17
ELECTROMAGNETIC COMPATIBILITY........................................................................................................................... 18
NOTES .............................................................................................................................................................................. 22
Technical Support
Technical assistance is available Monday through Friday,
8:00 am to 6:00 pm (Eastern Standard Time).
Phone: [phone]
Fax: [phone]
Customer Service: 800-659-6560

3
043565 R04
34488
046725 REV 2, 12/09
OPERATORY CABINET
RDCD-C
IEC Type B, Class 1
(120VAC, 12A, 60Hz)
MN
SN
MO
YR
Conforms to: UL STD 60601-1
Certified to:CAN/CSASTD C22.2 NO. 601.1
Technical Description
Model Designation: Centennial Rear Delivery Center
Power Supply: 120V~60Hz 15A Service
Protection against harmful ingress penetration of
water:
ordinary equipment
Foot switch protected against dripping water IPX 1.
GENERAL INFORMATION
Product Disposal
Contact your local authorized dealer for proper
disposal of the device to ensure compliance with
your local environmental regulations.
Interference with Electromedical Devices
To guarantee the operational safety of electromedical
devices, it is recommended that the operation of
mobile radio telephones in the medical practice or
hospital be prohibited.
Strong EMI sources such as electro surgery units or
x-ray units may affect performance. If performance
problems occur, move the unit to another electrical
circuit or physical location.
Incompatible Units or Accessories
To guarantee the operational safety and function
of this device, the use of unapproved unit or
accessories is not advised. Doing so could result in
potential hazard. Use authorized accessories and
devices only.
Product Identication

This label states the unit model and serial number,

SAMPLE labels shown
below.
Denition of Symbols
The following symbols and terms may be used
throughout this manual:
WARNING: Failure to carefully follow the
described procedure may result in damage
to the equipment and/or injury to the patient/
operator.
Risk of electrical shock present.
Make sure power is disconnected before
attempting this procedure.
Authorized European Representative:
Medical Device and QA Services
76, Stockport Road

United Kingdom
e-mail: [email protected]
See operating instructions.
(AC) Alternating current.
Protective earth (Ground)
Manufacturing Date
Waste Electrical and Electronic Equipment.
Type B Applied part.
Conforms with the Essential Requirements of the
European Medical Device Directive 93/42/EEC for
Class I Devices.
Conforms with the Essential Requirements of the
European Medical Device Directive 93/42/EEC for
Class IIa Devices.
Indicates conformity to General Requirements for

General mandatory action required, important to


Off
On
Light Switch
0473
Working Environment

only. It is not safe to use it where there is

Storage Conditions: The device is appropriately
packaged in a box. If product is to be stored before
installation, storage and handling instructions in
the packaging should be adhered to. Handling and
storage conditions are marked on the box.
Temperature: -68°F to 122°F/ -50°C to 50°C
Relative Humidity: 10% to 80%
if the device is not to be used for some time, ensure

before the master switch is switched off.
34488
0473
046817 REV 4, 01/10
DENTAL UNITS
SET20
IEC Type B, Class 1
(115VAC, 8A, 60Hz)
MN
SN
MO
YR
Conforms to: UL Std. 60601-1
Certified to: CAN/CSA Std. C22.2 NO. 601.1
Conforms to: EN Std. 60601-1 IEC Std.60601-1

4043565 R04
Use only Pelton and Crane replacement
parts. All repairs should be performed by
authorized Pelton & Crane Dealer/ or their
representatives.
This operatory cabinet is not for use in rooms where an explosion hazard exists.
As manufacturers of electro-medical products we can assume responsibility for safety-related performance of

authorized for this purpose, and if components affecting safe operation of the unit that may be needed are
replaced with original parts.



SAFETY
Please read the safety warnings and instructions before using the device. The manufacturer’s liability is applicable
only if the device is used in compliance with the directions and safety warnings provided in this manual. Safety
warnings are spread throughout the manual.
WARNING: Only authorized service
technicians should attempt to service this
equipment. Use of other than authorized
technicians will void the warranty.
WARNING: Use a licensed electrician for
all wiring.
WARNING: Failure to disinfect equipment
between patients could expose user/
patient to cross contamination and bio-
burden/bio-contamination.
WARNING: To avoid risk of electric shock,
this equipment must be connected only to
supply mains with protective earth.
WARNING: Power cords and their
associated parts cannot be substituted
without increased risk of electric shock or

replacement parts only! Power cords must be

service loops, strain reliefs, and cord guards
are in place and that line, neutral and ground
wires are secured.
WARNING: A dental unit may include
magnets in the construction of the
device which may temporarily affect
the function/programming of some

If the implanted device is programmed to
respond to a magnet, people who have
these types of devices should avoid dental
units with magnets.
WARNING: This product must be
disinfected before use.
WARNING: Failure to use protective gloves
can expose operator and patient to cross-
contamination.
WARNING: Dental instruments and
accessories are sharp - use care when
near the dental unit.
WARNING: Failure to return handpieces
to proper location could result in alternate
or additional handpieces operating without
notice.
WARNING: Proper personal protective
equipment (PPE), including, but not limited
to, gloves and eye protection, must be used
when operating the dental unit.
WARNING: Failure to install the syringe
tip correctly can result in injury or damage.
Refer to the documentation that came with
the syringe for full instructions on proper
installation and use.

equipment is allowed.
Ensure that the J-box, delivery head and
PMU covers are in place before operating the
dental system. Failure to follow instructions
may cause electric shock or other injuries.
Refer to the Installation Instructions,
Use & Care manual and accessory
manufacturer’s literature to install and
operate safely.

WARNING: This product is intended for
use by trained dental/medical professionals
only.

5
043565 R04
Upper
storage
Control
panel
POWER
AUX.
1
AUX.
2
MODE
TIMER
The
Centennial
Midsection
Assistant’s
instrumentation
Work surface
Doctor’s delivery
system
Foot control
Base
section of
cabinet
(Shown with Model 2222 Instrument Delivery System
& Model 2238 Assistant’s Instrumentation)
CENTENNIAL REAR DELIVERY OVERVIEW

6043565 R04
Instrument Delivery System Functions
WARNING: Maximum additional weight
that can be added to the control is 3 lbs.
Do not exceed the maximum weight capac-
ity.
Flush Function

handpieces with water when activated. Hold the
handpieces over a suitable container and activate

for at least 20 seconds.

activated after each patient. This helps eliminate
possible bacterial contamination in handpieces and
water lines.
Air Coolant Control Valve
This valve controls the amount of coolant air that is
supplied to the handpiece in use.
Water Control Valve

The controls are laid out so as to correspond with
the handpieces in use.
Master On/Off Toggle
This toggle activates the control head. It must be in
the “OFF” position when not in use.
WARNING:
it is required that the control head Master
On/Off Toggle (D) be in the “OFF” position
when not in use.
Control Head Touch Pad
The electronic touch pad allows the user to adjust
the chair’s manual positioning using the direction-
al arrows shown. The user can also program and
access the chair’s automatic positions using the

button. If the chair is equipped with chair mounted
light, the light may be activated using the light sym-
bol button (the toggle switch on the light head must
be in the “on” position for this function to operate).
Scaler Control Valve
This valve adjusts the speed intensity for the scaler.
To obtain maximum speed, turn valve clockwise fully
and depress the foot control completely. To lower
speed, turn the valve counterclockwise. Scaler will
deactivate when returned to the handpiece holder.
Handpiece Oil Collector
The handpiece oil collector is located on the under-
side of the delivery head. It collects the excess oil
coming from the handpieces. Before using the hand-
pieces, remove the collector by turning it counter-
clockwise. Place 3 pieces of 2 x 2 gauze inside the
collector. Reinstall collector but do not overtighten.
OPERATION
Control Head Touchpad

7
043565 R04
Testing and Adjusting Instrument
Delivery System
Ensure that the Master On/Off toggle is in the “OFF” posi-
tion. Turn on the manual air and water valves (located at
the utilities) inside the left side panel door. Make a visual
and audible inspection for leaks.
position and
make a careful inspection for leaks in the following areas:
a) Utility Cabinet
b) Instrument Delivery System;
tubing and manifold connections.
c) Internal plumbing of the
Instrument Delivery System
settings at
the utilities (located inside the cabinetry) are set as follows:
Air - 70-80 PSI
Water- 35-40 PSI
Turn regulator knobs clockwise to increase pressure and

accurate pressure reading, bleed off the air pressure by
using the air syringe button. Adjust air pressure in half-turn
steps.
 and also
check the spray pattern. Place all handpieces tubings into
-
strument delivery system. A steady stream of water should

Ensure that the handpieces to be installed have the proper
connectors for the supplied tubings.
Install the connectors onto handpieces and place hand-
pieces into their appropriate holders. Standard handpiece
positions for a right-handed operator is as follows (viewed
from left to right):
(1) Air/Water Syringe
(2) High/Low Speed
(3) High/Low Speed
(4) High/Low speed
(5) Optional handpieces or High/Low
Flush Toggle
Master
On/Off
Toggle
OPERATION

8043565 R04
Testing and Adjusting the
Instrument Delivery System (Cont’d)
Locate the auto block in the instrument
delivery system. To adjust handpiece air,
locate drive air adjustment stems and install
handpiece to connector. Activate foot control
(see Foot Control Operation) while observ-
ing the reading on drive air pressure gauge.
Using the drive air adjustment stems, adjust
handpiece pressure to manufacturer’s require-
ments.
Check water spray pattern of each handpiece.
Rotate water control valve counterclockwise

air control valve counterclockwise will in-

Foot Control Operation
The foot control controls drive air and cool-
ant water for the treatment instruments.
• For Drive Air: Depress the center pedal.
For more drive air, further depress pedal.
• For Coolant Water and Air: Switch the tog-

center pedal.
• Further depressing the pedal will gradually
increase drive air and coolant water/air
when activated.
Drive Air Pedal
On/Off
Toggle
OPERATION
WARNING: 
without a bur in the chuck. Extend-
ed running with no load can dam-
age the handpiece.
#1
#2
#3 #4
Master
ON/OFF
Toggle
Drive Air
Gauge
Air Coolant
Control Valve Water Flow
Control Valves

9
043565 R04
POWER
AUX.
1
AUX.
2
MODE
TIMER
The
Centennial
Switched
Aux.1
Aux.2
Switched
Continuous
4 Amp. Power
Strip
Right Side Frame of Cabinet
4 amp.
Electrical
Outlet
4 amp. Electrical
Outlet
(C)
(D)
Left Side Frame of Cabinet
(E)
(F)
(G)
(B)
(J)
CABINETRY FUNCTIONS
Auxiliary Outlets (F)
The two (2) outlets in the power strip labeled
Aux. 1 and Aux. 2 are operated from the cab-
inet’s control panel. When an accessory is
plugged into these outlets, it is remotely con-
trolled through the control panel’s auxiliary
switches (H) (see “Operating Control Panel”, in
the Use & Care).
Florescent Light (J)

automatically activated when the power supply

Electrical Supply
WARNING: The total electrical capacity
for the cabinet is listed at 12 amps., 15
amp. circuit breaker service. Ensure
optional equipment that is plugged into
the outlets does not exceed 12 amps.
site.
master pow-
er switch (A).
will illumi-
nate to indicate power is available.
Electrical power for the cabinet is supplied by the
115V main power source for the operatory.
The AC electrical outlets (one located in the mid-
section (B), one in the right side frame (C) and
the continuous outlets (D) located in the left side
frame’s 4 amp. power strip (E) will have power
available at all times after the operatory support
center (OSC) is connected with the power source
in the operatory.
The 4 amp. power strip (E) that is located in the
left side frame, also consists of auxiliary outlets
(F) and switched outlets (G) that are operated
from the cabinet’s control panel.
Turn control panel master power 
to operate these two outlets.
POWER
AUX.
1
AUX.
2
MODE
TIMER
The
Centen
nial
AH
Main Power
Switch
Control Panel

10 043565 R04
The control panel is located in the upper center section.
This panel controls power to the auxiliary equipment
and the year, month, date, and time can be set. A timer
is also available when monitoring the time for a dental
procedure.
The control panel is powered by the cabinetry’s main
 

illuminate to indicate power is available.
When accessories are plugged into the auxiliary outlets
located in the side of the cabinet, they are remotely con-
trolled through the control panel’s auxiliary switches (B &
C). Ensure power is on to the control panel. Press the
Aux. 1 and Aux. 2 switches to operate optional equipment.
Press buttons once more to turn power off.
To set the panel’s functions, proceed as follows:
• 

indicate power is available.
• As previously stated, when accessories are plugged
into the auxiliary outlets, they are remotely controlled
through the control panel’s auxiliary switches (B & C).
To activate the auxiliary equipment, press Aux. 1 or
Aux. 2. Press auxiliary switch again to turn power off.
• An integrated clock (D) is located in the panel for
added convenience.
POWER
AUX.
1
AUX.
2
MODE
TIMER
The
Centen
nial
ABC
D
E
G
• Mode

press the Up(F) and down (G) switch to set. Press
Mode switch again to set month, hour and minutes.
Continue to press Mode switch and display will return
to time mode.
• TIMER (H): The timer is programmable from one
second to 99 minutes and 59 seconds.
The timer is set in one-second increments. To start
timer, press timer switch. Press the Up(F) or down
(G) button to set incremental seconds. When pressing
and holding the up or down buttons, the timer will set
seconds in automatic increments.
To activate the count-down time press the TiMer switch
once more. The display will start counting down. Once
count reaches zero, three (3) beeps will sound and

switch is pressed to deactivate it. To stop a countdown
or return to clock mode, simply press the TiMer switch.
CONTROL PANEL FUNCTION

11
043565 R04
WARNING: When using or replacing instrument
or syringe accessories, i.e., tips, drill bits, ensure
that accessories are securely engaged into the
instrument’s locking mechanism to prevent acci-
dental injury.

are returned to their original holders.
WARNING: Do not activate syringe while tip is
in direct contact with skin.
Vacuum is constantly supplied to the High Volume Evacua-
tor (A) and Saliva Ejector (B).
Levers on the HVE (A) and saliva ejector (B) valve bodies

lever downward. To

High Volume Evacuator (A)
The HVE accepts disposable and non-disposable tips with
an outside diameter of 7/16’’ (1.1 cm).
Saliva Ejector (B)
The saliva ejector accepts disposable and non-disposable
tips with an outside diameter of 1/4’’(.64 cm).
Assistant’s Instrument Holder (C)
The vacuum head pivots approximately 230°.
WARNING: Care must be taken when
using the saliva ejector or HVE. Do not point
the tip of the instrument directly on the patient’s
cheeks or gums.
C
Computer Storage (Models RD36C & RD42C)
Read computer system manufacturer’s recommended
safety, use & care and installation instructions.
The computer monitor is stored into the monitor storage
area (A) of the cabinet. Remove the access plug (B) lo-
cated in the monitor storage area (A) and open the cabi-
net’s right side panel door. Insert computer monitor cables
through the slot. Place CPU in the right side of base so
that the front of CPU is facing the side panel door. Follow
the computer system manufacturer’s installation procedure
and plug unit into the 4 amp outlet (C) located in the right
side panel frame.
POWER
AUX.
1
AUX.
2
MODE
TIMER
The
Centennial
B
A
C
D
Increase
Flow
Decrease
Flow
AB
ASEPTIC VACUUM OPERATION

12 043565 R04
CLEANING, DISINFECTING & STERILIZATION
IMPORTANT: Do not use powdered cleansers, scouring pads or abrasive scrubbers on any of
the painted, plastic or metal surfaces of this dental unit. To remove dried-on material, use a soft-
bristled brush and a solution of mild detergent.
Equipment can be cleaned with a solution of mild detergent and warm water. A variety of surface disinfectants are
available for use in dental treatment rooms. Some of these can cause discoloration of painted, plated or anodized
surfaces with repeated use. This can be minimized by careful adherence to the disinfectant manufacturer’s
instructions and by frequent washing with soap and water.
The Manufacturer strongly advocates the barrier
technique be used whenever possible to preserve the
      
possible disposable barriers should be used and changed
between patients. The barrier technique will ensure

of the equipment.
Unacceptable Disinfectants Conditionally Acceptable Disinfectants*

dental equipment and are not recommended. Use of
these products will void your warranty.
These disinfectants have been found to be the
least harmful to the equipment surfaces by our test
methods.
Disinfection & Sterilization
         
high priority for our customers and end users. OSHA, the
ADA and the CDC are also involved in this complex issue.
The Manufacturer will not attempt to specify the required
intervals for disinfection nor can it recommend the overall
best surface disinfectant. Please refer to the Infection
Control Recommendations published by the American
Dental Association for further information. The question
is often asked, “What should I use to disinfect my dental
unit, chair and light?” This question is more complex than
it seems because of the wide variety of products on the
market as well as formulations of the products changing
to meet the needs of increased asepsis.
Barrier Technique
Chemical Disinfection
Regardless of the chemical disinfectant used, it is
imperative that the equipment be thoroughly washed with
mild soap and warm water at least once per day. This
wash down will minimize the harmful effects of chemical
disinfectant residues being allowed to accumulate on the
equipment. When using chemical disinfectants, always
pay strict attention to the disinfectant manufacturer’s
directions. When using concentrated disinfectants,
measure the concentrate carefully and mix according
to package directions. Disinfectant solutions that are
relatively harmless to surfaces at their recommended
strengths can be corrosive at higher than recommended
dilution ratios.
WARNING: Disinfect only by wiping, no
spray disinfection. Please be aware that
Pelton & Crane expressly rejects any claims
for warranty or damages when using other
cleaning and disinfections solutions.
WARNING: *The Manufacturer makes
no representation as to the disinfectant

warranty expressed or implied that these
disinfectants will not damage the surface


warranty.
**Iodophor-based disinfectants will cause yellow staining on many surfaces.
Strong Phenols/Phenol Alcohol combinations
Sodium Hypochlorite/Household Bleach
Sodium Bromide
Strong Alcohol
Household Cleaners (Dental Equipment
Only)
Citric Acids
Iodophors**
Ammonium Chloride
Accelerated Hydrogen Peroxide (0.5%)
Chemical Composition
Quaternary Ammonium
Chemical Composition

13
043565 R04
CLEAN WATER SYSTEM
Maintenance
WARNING: Disinfect new water bottle prior
to use.
The water bottle system is designed to optimize the quality
of water being delivered to the handpieces and syringe.
The Clean Water System has three functions:

for patient use.

the syringe and handpiece tubings.
3. The unit can be purged with air to inhibit the growth of
 
NOTE: 
at the top of bottle to allow bottle to depressurize
when removing it from unit.
Disinfecting the bottle:
Fill bottle with the 100 ml disinfectant
solution, shake vigorously and let it
settle for 10 minutes. Shake again,
then rinse twice with water.
We recommend 100 ml of
disinfectant solution for
each application per week.
Always use a fresh mixture
every week.
In order to maintain a truly asepsis water system, daily and weekly cleaning procedures must be performed in a
consistent, regular manner. Failure to do so could result in contaminated water lines and a lower water quality
than is acceptable for patient use.
Once a month, activate the City/Bottle Water Switch ensuring that the switch functions properly. If any issues are
found, call an authorized service representative to replace the switch.
Once a month, activate the Foot Control toggle valve ensuring that the toggle valve functions properly turning the
water on and off to the handpiece. If any issues are found, call an authorized service representative to replace
the toggle valve.
1 part
(10 ml)
5.25% Sodium
hypochlorite
(household bleach)
9 parts
(90 ml)
Tap water
The Disinfectant Solution:
Once a month, visually check handpiece holders for excessive wear and handpiece activation. If any issues are
found, call an authorized service representative to replace.
Once a month, visually check handpiece tubing for wear and tear and any separation of the tubing from the
connector. If any issues are found, call an authorized service representative to replace.

authorized service representative to repair or replace.

14 043565 R04
WARNING: In order to mitigate the
risk of cross-contamination between
patients, disinfection and sterilization
of handpieces must occur after each
dental procedure. Refer to the
handpiece manufacturer’s instructions
and recommendations for sterilization
or disinfection procedures.


through the handpiece tubings. The need for this is

normal use, which can lead to stagnation and the potential


and end of each day. This may be done with or without
handpieces installed, but having handpieces on the

required.
NOTE: Some models may not come equipped
with the handpiece control head. Refer only to
the sections of this manual that pertain to your
particular unit.
CARE OF THE UNIT
Asepsis Automatic Control
Control Head and Arm
The control head and post can be cleaned with a solution
of mild detergent and warm water. A variety of surface
disinfectants are available for use in dental treatment
rooms. Some of these can cause discoloration of painted,
plated or anodized surfaces with repeated use. This can
be minimized by careful adherence to the disinfectant
manufacturer’s instructions and by frequent washing with
soap and water.
IMPORTANT: Do not use powdered cleansers,
scouring pads or abrasive scrubbers on any of the
painted, plastic or metal surfaces of this dental unit.
To remove dried-on material, use a soft-bristled
brush and a solution of mild detergent.
Handpiece Flush — Daily Maintenance
The weekly cleaning procedure should be performed at
least once a week, preferably at the start of the week
before treating patients. If the unit is to be stored for
any length of time, perform the weekly maintenance
routine immediately before and after storage.
1. Purge the unit with air.
2. Flush the system with disinfectant solution:
a. Turn the unit off. Empty the water bottle,
replacing the water with cleaning solution (see
Disinfectant Solution, page 13).
b. Hold the handpiece tubings and syringe
over the cuspidor or other suitable container.
Turn the unit on, wait a few moments, then

control until a continuous stream of solution is
running through the system.
3. Allow the disinfectant to remain in the unit for 10 to

Solution is used up.
4. Purge the unit with air:
a. Hold the handpiece tubings and syringe over a
container. Turn the unit on, wait a few


Allow adequate time for fresh water to make its way through the entire system and displace all standing water.
The American Dental Association and the Centers for Disease Control can provide additional recommendations

solutions in the self-contained water system.

and foot control until all Solution is purged from
the system.
b. Turn the unit off. (If the unit will be stored,
stop here)
5. Fill with clean water:
a. With the unit turned off, remove the empty
disinfectant bottle. Replace with clean bottle and
water.
b. Hold the handpiece tubings over a suitable
container. Turn the unit on, wait a few moments


Replace handpieces and do the same with the syringe.
The unit is now ready for use.
Weekly Maintenance
Handpiece Oil Collector:
Replace the 2 x 2 gauzes with clean gauzes in the
handpiece oil collector every 90 days or more often if
handpieces are oiled frequently.

15
043565 R04
ASSISTANT’S VACUUM INSTRUMENTS
Draw clear water through each valve, while opening
and closing it several times. Leave the valve open for
several seconds to allow all of the water to clear the
hoses. The HVE and Saliva Ejector tips should always
be replaced with sterile ones before each patient.
We recommend that you draw a vacuum system
sanitizing solution which is non-toxic and
environmentally safe through each valve, while
opening and closing it.
At least once a day the solids collector screen should
be cleaned or replaced as needed. Turn off the
vacuum pump before removing the solids collector

amount of material in the screen, more frequent
cleaning is necessary.
Clean the external surfaces of the vacuum instruments
using a solution of mild detergent and warm water.
Thoroughly rinse the syringe with clean water, then dry
with a clean, soft, lint-free cloth.

regulated by the thumb lever and that the HVE and SE are being cleaned and maintained properly.
Disassemble the valve and lubricate the internal parts when operation becomes stiff or sticky. Clean the inner
surfaces and apply a small amount of O-ring lubricant to the moving parts and O-rings.
After Each Patient
At the End of Each Day
Cleaning the Solids Collector
Cleaning
Sterilization
Remove each valve from its tubing for sterilization.
A vacuum plug may be inserted into the quick
disconnect while there is no valve in place.
In any situation involving high-risk patients, it is
recommended that the instruments be removed for
sterilization after every patient.
WARNING: Ultrasonic cleaning is not
recommended, as the chemicals used

instrument.
WARNING: Do not use sodium
hypochlorite or any chlorine bleach on
the vacuum instruments. These products
will permanently damage the instruments.

pads or abrasive scrubbers, any of which


16 043565 R04
Disinfecting the Surfaces
Disinfect cabinet surfaces by spraying or wiping with
surface disinfectant using the spray-wipe-spray tech-

Asepsis Procedures).
WARNING: Follow the manufacturer’s direc-
tions for use of disinfectants! Use only the dis-
infectants that have been tested and approved.
For additional infection control, as well as to reassure
your patients that you are following strong protective
practices, we strongly recommend the use of coverings
such as plastic, foil or treated paper or autoclavable
components (such as light handles, assistant’s instru-
mentation cover, tray mat, etc.) as well as the use of
surface cleaners and disinfectants either daily or fol-
lowing each patient, depending on the circumstances.
Cleaning the Surfaces
To remove dirt and disinfectant residues, clean the
surfaces regularly with a normal, commercial cleaning
agent.
WARNING:
Doing so can cause damage to the cabinet
surface.
Cleaning Agents
Because of their high concentration and the substances
they contain, many cleaning agents can affect surfaces
by dissolving, etching, bleaching or discoloring. Carefully
wipe surface with a damp cloth and use an appropriate
cleaning agent to lessen potential damage.
CLEANING CABINETRY SURFACES
Cleaning Stainless Steel Fixtures
Clean surface using warm water with a mild,
non-scratching abrasive powder such as typical
household cleanser. Do not use brushes or steel
wool as they may cause scratches and will leave
particles embedded in the surface which can lead
to rusting. For more aggressive cleaning, a small
amount of vinegar can be added to the cleanser.
Rinse the surface with warm water. Once thoroughly
rinsed, wipe the surface dry with a soft towel to
avoid water spots.
Stains resulting from normal use are the most com-
mon surface contaminates. Using glass cleaner,
spray and gently wipe the surface with a soft cloth.
Rinse thoroughly with warm water. Wipe the surface
dry with a soft cloth to avoid water spots.
Repair surface scratches using the following
technique: Using 120 grit emery cloth or paper,
-
sure. Once the scratch is removed, polish the
surface using a 3M scotch brite pad. Polish in the

is restored.

17
043565 R04
Instrument Delivery System Tension Adjustment:
Using a 3/32” Allen wrench, loosen the set screw (A) lo-
cated in the pivot arm. Using the 9/16” hex wrench, loosen
hex bolt (B) to decrease tension or tighten bolt to increase
tension according to the dentist’s preference. Tighten set

ADJUSTMENTS
A
Converting Unit to Left/Right or Right/Left Delivery:
Grasp hoses together to avoid hose interference and lift
up vacuum arm.
Pull the vacuum arm forward to unlock and tilt upward.
Swing the doctor’s control head underneath assistant’s
arm and move assistant’s arm to the new position.
When conversion is complete, push vacuum arm back to
lock in place.
B

require additional adjustments once unit is installed.
1. Water Filter/Regulator:
 35-40 psi
(275.8 kPa). To adjust, turn regulator knob clockwise
to increase pressure and counterclockwise to de-
crease pressure.
2. Air Filter/Regulators:
The air regulator should be set at 70-80 psi (551.7
kPa). To adjust, turn regulator knob clockwise to
increase pressure and counterclockwise to decrease
pressure.
2.
1.

18 043565 R04
ELECTROMAGNETIC COMPATIBILITY
Electrical medical devices are subject to special EMC safety measurements and as a result the
equipment must be installed according to the installation instruction manual.
PORTABLE ELECTRONIC DEVICES
Portable and mobile high frequency electronic communications equipment may interfere with
electronic medical devices.
STATIC SENSITIVE DEVICES
Where labeled, this equipment contains static sensitive devices that require special
precautions when handling. At a minimum, a grounded wrist strap that is connected to a
ground stud should be worn to reduce the possibility of damage to the unit.
MEDICAL ELECTRICAL EQUIPMENT
ELECTROMAGNETIC COMPATIBILITY
(TECHNICAL DESCRIPTION)
ELECTROMAGNETIC COMPATIBILITY testing has been done for this product.
ACCESSORY USE

result in an increase of electromagnetic emissions and/or a decrease in electromagnetic
immunity of the system. Do not use any accessories not authorized or approved by the
manufacturer.
INTERFERENCE FROM OTHER EQUIPMENT
If other equipment is used adjacent to or stacked with this equipment, the system must be
observed to verify normal operation.
MEDICAL ELECTRICAL EQUIPMENT ELECTROMAGNETIC COMPATIBILITY
(Instructions for use)
ATTENTION
OBSERVE PRECAUTIONS
FOR HANDLING
ELECTROSTAT IC
SENSITIVE DEVICES
ELECTROMAGNETIC COMPATIBILITY

19
043565 R04

customer or the user of this product should ensure that it is used in such an environment.
UTis the AC. mains voltage prior to application of the test
level.
Guidance and manufacturer‘s declaration-electromagnetic immunity
IMMUNITY TEST IEC60601 TEST LEVEL  

ELECTROSTATIC DISCHARGE
(ESD) IEC 61000-4-2
61000-4-2
+/-6 kV contact
+/-8 kV air
+/-6 kV contact
+/-8 kV air
Floors should be wood, concrete

covered with synthetic material
the relative humidity should be
at least 30%. Where labeled,
a ground strap (connected to
ground lug) should be worn
to reduce the possibility of
damaged to the unit when
servicing.
ELECTRICAL FAST

IEC 61000-4-4
Capacitive Clamp
+/-1 kV, 5/50 nsec pulse
+/-5 kHz repetition
frequency
Direct Injection
+/-2 kV, 5/50 nsec pulse
+/-5kHz repetition
frequency
Capacitive Clamp
+/-1 kV, 5/50 nsec pulse
+/-5 kHz repetition
frequency
Direct Injection
+/-2 kV, 5/50 nsec pulse
+/-5kHz repetition
frequency
Mains power quality should be
that of typical commercial or
hospital environment.
SURGE IEC 61000-4-5 +/-1 kV differential mode
+/-2 kV common mode
+/-1 kV differential mode
+/-2 kV common mode
Mains power quality should be
that of typical commercial or
hospital environment.
VOLTAGE DIPS, SHORT
-


IEC 61000-4-11
30% reduction, 500 ms
60% reduction, 100 ms
>95% reduction, 10 ms
>95% reduction, 5000 ms
30% reduction, 500 ms
60% reduction, 100 ms
>95% reduction, 10 ms
>95% reduction, 5000 ms
Mains power quality should
be that of typical commercial
or hospital environment. If
the user requires continued
operation during power mains
interruptions, it is recommended
that the product be powered by
an uninterrupted power supply or
battery.


61000-4-8
3 A/m 3 A/m 
should be at levels characteristic
of a typical location in a
typical commercial or hospital
environment.
ELECTROMAGNETIC COMPATIBILITY

20 043565 R04
NOTE 1: At 80 MHz to 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption

a
mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically


used exceeds the applicable RF compliance level above, the product should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting
or relocating the product.
b

customer or the user of this product should assure that it is used in such an environment.
Guidance and manufacturer's declaration-electromagnetic immunity
Portable and mobile RF
communications equipment should
be used no closer to any part of the
product, including cables, than the
recommended separation distance
calculated from the equation applicable
to the frequency of the transmitter.
Immunity Test IEC60601 Test
Level
Compliance
Level
Conducted RF
IEC 61000-4-6
3 Vrms
150 kHz to 80
MHz
Where P is the maximum output
power rating of the transmitter
in watts (W) according to the
transmitter manufacturer and d is the
recommended separation distance in
meters (m).
-

transmitters, as determined by an
electromagnetic site survey, (a) should
be less than the compliance level in
each frequency range. (b)
-
Interference may occur in the vicinity
of equipment marked with the following
symbol:
ELECTROMAGNETIC ENVIRONMENT
GUIDANCE
 
 
Radiated RF
IEC 61000-4-3
3 V/m
80 kHz to 2.5
MHz
3 Vrms
3 V/m
ELECTROMAGNETIC COMPATIBILITY
