2
PROBE CORD
No.
Name
Function
1
Lip hook connector
Install the lip hook.
2
USB connector (H)
Connects to the file holder.
3
USB connector (A)
Connects to the Apex Connect unit
INDICATIONS FOR USE
Apex Connect is an Electronic Apex Locator designed to measure
the working length of root canals.
CONTRAINDICATIONS
•
Do not use this device on patients with pacemakers or nerve
regulators. Also, do not use this device on patients who are
sensitive to metals such as stainless steel.
•
Do not use this device in the presence of oxygen oxides,
nitrogen oxides, or flammable anesthetic mixtures
containing air. There is a risk of explosion.
SAFETY PRECAUTIONS
To ensure the safety of users and patients and to use the device
properly, be sure to read the contents of this instructions for use
before using the device. The manufacturer is not responsible for
any injuries or damage caused by not following the precautions.
The most important thing when using medical devices is the
safety of all users, including patients and medical staff members.
Please read the following safety information thoroughly to
identify and prevent potential hazards.
WARNING
May cause serious damage or severe injury such as death if
not followed.
PRECAUTION
May cause physical injury or property damage, as well as, indicates
unsafe procedures or cases where the device may be damaged.
WARNINGS
•
For use by qualified and trained dental personnel only.
•
U.S. federal law restricts the sale of this device to or on the
order of a healthcare professional.
•
Do not use this device with electric surgical devices.
•
Use of other accessories that are not authorized for use in
connection with this device may cause malfunction and
compromise patient safety.
•
Do not use the device in a place that it is exposed to direct
sunlight, heat sources, or near a fire. The battery may
explode or cause a fire.
•
Never use a damaged cable. There is a risk of fire or
electric shock.
•
Be sure to connect the power plug to a grounded power
supply. There is a risk of fire or electric shock.
•
Do not touch electrical parts with wet hands. There is a risk
of electric shock and injury.
•
To prevent accidental aspiration, the use of a rubber dam is
strongly recommended.
•
Use the battery, AC/DC adapter, and power cord included in
the package. Only use Kerr Endodontics batteries designated
for this system. Use of other batteries may damage the
device(s) or cause a malfunction.
•
Ensure conductors such as metal are not in contact with
the metal part of the device. There is a risk of device
malfunction, fire, or electric shock.
•
Do not disassemble the device. Direct physical contact with
the inside of the device can cause electrical shock and burns.
•
Do not repair, modify, or disassemble the device, except for
authorized service engineer or a specialist who has received
repair training. Product failure or damage caused by
unauthorized actions is not subject to free service and
warranty service.
•
When transporting the device, use the original packaging
provided by manufacturer to prevent accidental activation
of the unit or any damage to the device itself.
•
Air or land transportation of the device is permitted in the
original packaging container.
•
For shipping batteries within the United States or
Internationally, consult the Department of Transportation’s
Pipeline and Hazardous Materials Safety Administration or
the International Air Transport Association guidelines.
PRECAUTIONS
•
Do not use this device for any purpose other than its
intended use. The manufacturer is not responsible for any
injuries or damage caused by this.
•
This device is not waterproof. Do not submerge or directly
contact the device with water. There is a risk of electric
shock or device malfunction.
•
Do not connect unsupported types of devices. The device
may break down or malfunction.
•
When using or moving the device, do not throw or drop it.
The device may break down or malfunction.
•
When using, be fully aware of the protective measures for
the patient and be prepared for possible risks.
•
Check the patient's condition and device operation
during use.
•
If the device is dropped during use, ensure that there is no
danger to the patient or user.
•
For long-term storage, keep the device in a clean and
dry place, where the temperature and humidity do not
change easily.
•
If there are sign of smoke or burning, turn off the power
immediately, and take appropriate measures.
•
If the device breaks down or has a problem, stop using it
immediately, and contact customer services.
ADVERSE REACTIONS
None known.
SYMBOL DESCRIPTION
Full explanation of symbols used on Kerr packaging is located at:
http://www.kerrdental.com/symbols-glossary
Serial number
Authorized representative in the European Community
Manufacturer
CE - Mark and identification number of notified body.
Product conforms to the essential requirements of the
Medical Device Directive 93/42/EEC
Type BF Applied Part
Humidity limitation
Fragile, handle with care
This way up
Sterilizable up to the stated temperature
