Warranty; Service; Power Supply; Technical Data - DENTSPLY Smartlite iQ Manual De Funcionamiento E Instrucciones De Uso

• Prior to disinfection, thoroughly wipe all surfaces and the power
supply plug, clean with a damp towel (with mild detergent if
needed). Properly discard used towel.
• The unit may be disinfected using an EPA registered non-immer-
sion surface disinfectant, carefully following the instructions
provided by the disinfectant solution manufacturer. Water based
disinfectant solutions are preferred. Alcohol or glutaraldehyde
based solutions may be harmful and may discolor plastic
materials. Use of alcohol or glutaraldehyde based disinfectant
solutions will void the SmartLite IQ unit warranty.
• DO NOT immerse unit in water or disinfectant. Wipe — do not
spray — solution (with curing probe in place) onto plastic parts.
Prevent liquids from entering openings on unit.
• Remember to reconnect the power supply plug to the charging
base unit when cleaning process is completed.

WARRANTY

This product is designed for use in a dental office and this
warranty is not applicable to other uses. DENTSPLY warrants this
product against defective materials and workmanship for a period
of twenty four (24) months from the date of purchase. In the event
of such a defect, DENTSPLY will repair or replace the product or
necessary parts therein, at its discretion, and such repair or
replacement shall be the sole remedy of this warranty. This
warranty extends only to the original purchase and is subject to
these conditions:
1. Fiberoptic curing probes are excluded from this warranty.
2. The unit must not be subjected to abuse, improper installation
or application, nor repair service by other than trained
DENTSPLY service personnel.
THERE ARE NO WARRANTIES, EXPRESS OR LIMITED, WHICH
EXTEND BEYOND THIS DESCRIPTION. DENTSPLY neither
assumes, nor authorizes any person to assume for it, any other
liability in connection with the sale and use of this product.
DAMAGES ARE LIMITED STRICTLY TO REPLACEMENT OF THE
PRODUCT. DENTSPLY EXPRESSLY DISCLAIMS LIABILITY FOR
INCIDENTAL AND CONSEQUENTIAL DAMAGES RESULTING
FROM ITS USE.
Claims covered by this warranty will be honored when this
warranty is presented within 30 days from discovery of defect.
During the warranty period, DENTSPLY International reserves the
right to repair or replace this product.

SERVICE

For product service please contact DENTSPLY Caulk customer
service at 1-800-532-2855 ext. 249. Customers outside the USA
should contact their nearest DENTSPLY location, as listed in back
of this manual.

POWER SUPPLY

This device should only be used with a power supply which
appears below:
Dentsply
Reorder# Model
644016 GTM3T48-12-1200D (US)
644014 GTM3T48-12-1200D-3 (EU)
644021 GTM3T48-12-1200D-4 (UK)
644015 GTM348-12-1200D (Japan)

TECHNICAL DATA

Model 100
AC Input Rating:
DC Output Rating: 12vDC, 1200ma
Protection from
electric shock:
Protection against
ingress of water:
Operation Mode:
Operating Environment:
NOTE: Equipment not suitable for use in the presence of a
Temperature:
Relative Humidity:
Atmospheric Pressure:
Transport and Storage Conditions:
Temperature:
Relative Humidity:
Atmospheric Pressure:
Dimensions:
Charging Base Height:
(with handpiece):
Charging Base Width:
Charging Base Length:
Charging Base Weight:
power supply plug length:
Handpiece Length (w/o probe): 6.6 inches (16.8 cm)
Handpiece Width:
Handpiece Height:
Handpiece Weight (w/o probe): 8.0 ounces (0.23 kg)
Complies with the following Directives/Standards:
93/42/EEC
IEC 601-1
IEC 601-1 Am.1
IEC 601-1 Am.2
EN 60601-1
EN 60601-1-2
CSA C22.2 no.601.1
UL 2601-1
Voltage
120v
230v
240v
100v
10
Reorder #644010: 120v
Reorder #644011: 230v EU
Reorder #644012: 240v UK
Reorder #644013: 100v
Type BF Applied Part
IEC Equipment Class II/Internally Powered
(Ordinary Equipment) IXPO
Continuous operation with intermittent loading:
(1 min./5 min. = 1 min. On/5 min. Off)
flammable anesthetic mixture with air or with nitrous oxide
50°-86°F (10°-30°C)
10% to 75% (non-condensing)
700 to 1060 hPa
14°-140°F (-10°- +60°C)
10% to 100%
500 to 1060 hPa
4.8 inches (12.2 cm)
5.9 inches (15 cm)
2.9 inches (7.4 cm)
7.2 inches (18.3 cm)
12 ounces (0.34 kg)
72 inches (183 cm)
1.4 inches (3.5 cm)
5.0 inches (12.7cm)
MDD Directive
1988 – Medical Electrical Equipment
(General Requirements for Safety)
1991 – Amendment 1 to IEC 601-1
1995 – Amendment 2 to IEC 601-1
1993 – Medical Electrical Equipment
(General Requirements for safety)
Amendments 1-13.
1993 – Medical Electrical Equipment Part
1: General requirements for safety 2:
Collateral standard: Electromagnetic com-
patibility – Requirements and tests
M90-Medical Electrical Equipment Part 1:
General requirements for safety
(Amendment 1 and 2)
2nd Edition – Medical Electrical
Equipment: Part 1: General Requirements
for safety