ASI 90-2115 Installation and operating instructions

ASI MEDICAL INC. | 8811 American Way, Suite 130, Englewood, CO 80112
Advanced Dental Systems® & Advanced Endodontic Systems®
Customer Support Team | www.asisupport.com | 303-407-6072
ADVANCED SELF-CONTAINED
DENTAL SYSTEM
Operation & Service Manual
Document No. 65-OS08, Rev-B, April 27, 2021
Dental Operative Unit
Models: 90-2115 | 90-2125
This guide provides important steps for setup, use, and maintenance of the ASI delivery system.
It includes important details which must be followed to ensure safety and proper use.
This document includes sections for optional components that may or may not be included in your
system. Your system may contain built-in accessory instruments from other manufacturers.
Please refer to the original manufacturer’s instructions for operation and maintenance for those
instruments.

Contents
Operation & Service Manual, Advanced Self-Contained Dental System
www.asisupport.com 65-OS08 Rev-B (04/27/21)
1SYMBOLS & SAFETY PRECAUTIONS
2OPERATING ENVIRONMENT & CLASSIFICATION OF EQUIPMENT
3PRODUCT DESCRIPTION, SPECIFICATIONS & WARRANTY
Intended Use
Product Description / Theory of Operation
Dimensions, Specifications & Technical Data
Warranty Information
4UNPACKING & INSTALLATION
5START UP, OPERATION & SHUT DOWN
6CLEANING/DISINFECTING, STORAGE & SHIPPING
7TROUBLESHOOTING
8SERVICING & PREVENTATIVE MAINTENANCE
9SCHEMATICS, DIAGRAMS & PARTS LISTING
10 REFERENCES OR SUPPLEMENTAL INFORMATION (OPTIONAL)

Section 1 Contents
Symbols & Safety P
recautions
www.asisupport.com 65-0047 Rev-A | 11/12/20
SYMBOLS
DESCRIPTION OF DANGER LEVELS
GENERAL SAFETY PRECAUTIONS
IDENTIFICATION OF SYMBOLS
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SYMBOLS & SAFETY PRECAUTIONS
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SYMBOLS
These symbols are used in this manual.

Important information for users and technicians
⚠
Warning Symbol
DESCRIPTION OF DANGER LEVELS
⚠
⚠DANGER
DANGER indicates a maximum hazardous situation that can directly cause serious injury of death.
⚠
⚠WARNING
WARNING indicates a hazardous situation that can lead to serious injury of death.
⚠
⚠CAUTION
CAUTION indicates a hazardous situation that can lead to property damage or minor to moderate injury.
GENERAL SAFETY PRECAUTIONS
In addition to observing the normal precautions associated with standard dental practices and procedures, the
following precautions should be strictly noted and observed during the set-up, operation, and maintenance of
this system.
⚠
⚠WARNING
COMPRESSED AIR
The compressed air system that operates this unit is under pressure. Compressed air can propel dust or loose particles and
can
cause bodily injury or damage. Always turn the system off and bleed off air pressure before attaching or removing air lines o
r
accessories or servicing this unit. All air lines should be periodically inspected and replaced if worn or damaged.
If an o
utside compressed air supply is used to power this unit, the air supply must be regulated to 80 psi or below. Excessive air
pressure could cause certain components to rupture.
⚠
⚠
WARNING
ELECTRICAL VOLTAGE
This system is powered by high voltage
electricity. Like any other electrically powered device, if it is not used properly, it can
cause electrical shock. Always plug the power cord into an electrical outlet with adequate fuse protection and proper grounding.
In the event of a short circuit, gr
ounding reduces the risk of shock by providing an escape wire for the electric current. Improper
grounding of the unit can result in a risk of electric shock. Always unplug the unit before doing any service or repair to the unit.
⚠
⚠WARNING
PRESENCE OF HEAVY METALS/AMALGAM
This
system may be equipped with optional suction instruments. As part of dental procedures, particles of amalgam may be
suctioned into the dental suction handpieces and collected within the system and trap filter.
Recycle amalgam in accordance
with local guidelines.
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⚠
⚠WARNING
INFECTIOUS MATERIALS
Infectious disease workplace safety protocols to safeguard against cross contamination of infectious disease should always
be
observed. When maintaining the suction system or emptying the contents of the suction waste
container, safe precautions and
practices including the wearing of face mask, eye protection and gloves are to be followed.
⚠
⚠WARNING
QUALIFIED PERSONNEL ONLY
The
product should only be operated by qualified personnel only. The operator bears responsibility for the correct settings and
proper use of the system. ASI Medical, Inc. (ASI) cannot be held liable for any malfunction of this product, or performance
failure and/or its designed or desired utility, nor can ASI be held liable for injuries
to persons or animals, in any case when the
device is misused or not operated, applied or maintained in strict accordance with user/owner instructions set out in the
operation manual. In the event of any doubt or question, the user is to contact ASI for clarification or assistance.
⚠
⚠
WARNING
ELECTROMAGNETIC COMPATIBILITY (EMC)
Changes or modifications to this product not expressly approved by the manufacturer may result in increased emissions or
decreased immunity performance of the product and could
cause EMC issues with this or other equipment. This product is
designed and tested to comply with applicable regulation regarding EMC and shall be installed and put into service according
to
the EMC information stated below:
⚠
WARNING
Use of portable phon
es or other portable or mobile radio frequency (RF) emitting equipment near the product may cause
unexpected or adverse operation.
⚠
WARNING
The use of accessories, transducers
, and cables other than those supplied may result in increased emissions or decreased
immunity performance of the product. The product shall not be used adjacent to, or stacked with, other equipment. If adjacent
or stacked use is necessary, the user shall be responsible to test to verify normal operation in the configuration in which
it is
being used.
⚠
⚠
CAUTION
DAMAGE FROM UNSUITABLE ACCESSORIES
Responsibility for the use of accessories, parts or assemblies from other manufacturers rest solely with the user.
⚠
⚠CAUTION
CAUSTIC OR CORROSIVE CHEMICALS
The irrigation system
may contain chemicals that are caustic or corrosive. Always verify with the operator of the system to
determine which chemicals they are using within the system. Always follow workplace safety protocols when doing
maintenance or service of the system inclu
ding the wearing of face mask, eye protection and gloves for proper protection of
exposed skin, breathing and eyes.
⚠
⚠
CAUTION
CORRECT OPERATING VOLTAGE
Check the correct operating voltage on the rating plate and ensure that the product is correctly
configured for the voltage
before plugging in and energizing.
⚠
⚠CAUTION
SUCTION CANISTER PURGE
LED turns on when suction canister overfills.
⚠
⚠CAUTION
POWER SUPPLY CORD
The power supply cord is not replaceable by service personnel.

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IDENTIFICATION OF SYMBOLS
The table below defines symbols that may be included on/in this delivery system.
Symbol
Description
Conforms to UL STD 60601-1; Certified to CSA STD C22.2 NO. 601.1
Recognized by Underwriters Laboratories Inc. with respect to electric shock, fire, and mechanical hazards only in
accordance with UL 61010-1 (2601-1) and under mutual recognition agreement with CAN/CSA C22.2, No.601-1.
Protective earth (ground)
Functional earth (ground)
Attention, consult accompanying documents. No user serviceable parts. Attention, line voltage. Only licensed electrician
should remove cover.
Type B applied part
Type BF applied part
Class II Equipment
Caution: Metal surfaces can be hot during and following the dry cycle.
Marking on the outside of Equipment or Equipment parts that include RF transmitters or that apply RF electromagnetic
energy for diagnosis or treatment.
Manufacture
Consult user information
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Section 2 Contents
Operating Environment & Classification of Equipment
www.asisupport.com 65-0048 Rev-B (04/01/21)
CLASSIFICATION OF EQUIPMENT (EN-60601-1)
ENVIRONMENTAL SPECIFICATIONS
ELECTROMAGNETIC COMPATIBILITY (EMC)

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CLASSIFICATION OF EQUIPMENT (EN-60601-1)
Type/Mode
Classification
Types of shock protection
Class I Equipment
Degree of shock protection
TYPE B and/or TYPE BF APPLIED PART depending on order configuration
Degree of protection against water ingress
ORDINARY EQUIPMENT
Mode of operation
Intermittent
Flammable Gasses:
Not suitable for use in the presence of a flammable anesthetic mixture with air,
oxygen, or nitrous oxide, where such gasses may accumulate in concentration
(closed spaces).
ENVIRONMENTAL SPECIFICATIONS
Temperature/Humidity
Specification
Storage/Transportation Temperature:
-40˚C to 70˚C (-40˚F to 158˚F) - Relative humidity 80%
Operating Temperature:
10˚C to 40˚C (40˚F to 104˚F) - Relative humidity 80%
Indoor Use:
Altitude up to 2,000M (6,563 ft.), installation category II, pollution degree 2. (UL
61010A-1 and CAN/CSA C22.2, No. 1010.1-92 only)
Exclusions
Hospitals except for near active HF surgical equipment and the RF shielded room of a
medical equipment system for magnetic resonance imaging, where the intensity of
electromagnetic disturbances is high.
ELECTROMAGNETIC COMPATIBILITY (EMC)
Although this dental equipment conforms to the intent of the 2004/108/EC EMC Directive, all medical
equipment may produce electromagnetic interference or be susceptible to electromagnetic interference. The
following are guidance and manufacturer’s declarations regarding EMC for this equipment.
This equipment needs special precautions regarding EMC and needs to be installed and put into service
according to the EMC information provided in the following pages.
⚠
⚠
WARNING
ELECTROMAGNETIC COMPATIBILITY
As with all electrical medical equipment, this equipment may cause radio interference or may disrupt the operation of nearby
equipment. It may be necessary to take mitigation measures such as re
-orienting or relocating this equipment unit or shielding
the location.
•Portable and Mobile RF communications equipment can affect the performance of this equipment,
and should be used no closer than 30cm (12inches) to any part of the ASI dental system. Please use
the guidelines and recommendations specified in IEC 60601-1-2, Edition 4.0.
•Other medical equipment or systems can produce electromagnetic emissions and therefore can
interfere with the functionality of this equipment. Care should be used when operating the system

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adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, this equipment
should initially be observed to verify normal operation in the configuration in which it will be used.
•The electrical cables, external power supplies and accessories listed or referenced in this manual
have been shown to comply with the test requirements listed in the following tables.
Care should be taken to use only manufacturer-recommended cables, power supplies and electrical
accessories with this equipment.
If the user or a third-party supplier offers cables, external power supplies and electrical accessories
for use with this equipment and they are not listed or referenced in this manual, it is the
responsibility of that third-party supplier to determine compliance with the standards and tests in
the following tables.
•The use of electrical cables and accessories other than those specified in this manual or referenced
documents may result in increased electromagnetic emissions from this equipment or decreased
electromagnetic immunity of this equipment.
Guidance and Manufacturer's Declaration Electromagnetic Emissions
This equipment is intended for use in the electromagnetic environment specified below. The customer or the end user of this
equipment should assure that it is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment - Guidance
RF Emissions - CISPR 11
(Radiated & Conducted)
Group 1
This equipment uses RF energy only for its internal function. Therefore, its RF
emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
RF Emissions - CISPR 11
(Radiated & Conducted)
Class A
The emissions characteristics of this equipment make it suitable for use in
industrial areas and hospitals. If it is used in a residential environment this
equipment might not offer adequate protection to radio-frequency
communication services. The user might need to take mitigation measures, such
as relocating or re-orienting the equipment.
Harmonic Emissions
EN/IEC 61000-3-2
Class A
Voltage fluctuations/
Flicker Emissions
EN/IEC 61000-3-3
Complies

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Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
This equipment is intended for use in the electromagnetic environment specified below. The customer or the end user of this
equipment should assure it is used only in such an environment.
Immunity Test
EN/IEC 60601
Test Level
Compliance Level
Intended Electromagnetic
Environment
Electromagnetic Discharge (ESD)
EN/IEC 61000-4-2
± 8kV contact
± 2kV, ± 2kV, ± 8kV, ±
15kV air
± 8kV contact
± 2kV, ± 2kV, ± 8kV, ±
15kV air
Floors should be wood, concrete or ceramic
tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30%.
Electrical fast transient/burst
EN/IEC 61000-4-4
± 2kV for power supply
lines
± 1kV for input/output
lines
± 2kV for power supply
lines
± 1kV for input/output
lines
Mains power quality should be that of a
typical commercial or hospital environment.
Surge
EN/IEC 61000-4-5
± 1kV differential mode
(line-line)
± 2kV common mode
(line-earth)
± 1kV differential
mode (line-line)
± 2kV common mode
(line-earth)
Mains power quality should be that of a
typical commercial or hospital environment.
Voltage dips, short interruptions
and voltage variations on power
supply input lines
EN/IEC 61000-4-11
0 % UT; 0,5 cycle at 0°,
45°, 90°, 135°, 180°, 225°,
270° and 315°
0 % UT; 1 cycle and 70 %
UT; 25 cycles Single
phase: at 0°
0 % UT; 250 cycle
0 % UT; 0,5 cycle at 0°,
45°, 90°, 135°, 180°,
225°, 270° and 315°
0 % UT; 1 cycle and 70
% UT; 25 cycles Single
phase: at 0°
0 % UT; 250 cycle
Mains power quality should be that of a
typical commercial or hospital environment. If
the user of this equipment requires continued
operation during power mains interruptions,
it is recommended that this equipment be
powered from an uninterruptible power
supply or a battery.
Power frequency (50/60Hz)
magnetic field
EN/IEC 61000-4-8
3A/m
3A/m
Power frequency magnetic fields should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.