Dentsply Sirona EndoActivator Mode D'emploi page 18

4) PRECAUTIONS
1) The EndoActivator
2) The EndoActivator
functions as intended when the original component parts are used together. With the use of non-original
components, serious consequences may result. The original components include the EndoActivator
handpiece, the Activator tip and protective barrier.
The Dentsply Sirona reference number of the handpiece is
The reference numbers of the Activator tips include
The reference number of the protective barrier is
3) The handpiece provides 3-speed sonic motor options (High, Med, Low). The power settings used are
ultimately determined by the procedure to be performed, the clinician's experience, and the power
needed to efficiently complete the clinical task.
4) The EndoActivator
5) All endodontic procedures should be performed with an EndoActivator
over the handpiece.
6) The Activator tip should be disinfected before use, or contamination of the root canal may result.
7) Proper use of the EndoActivator
8) Improper handling of the EndoActivator
the rocker arm.
9) Activator tips and protective barriers are intended for single-patient use only. Cross contamination may
occur to the patient if tips and barriers are re-used.
10) Proper disposal of Activator tips and protective barriers is required in accordance with local laws and
regulations.
11) Proper disposal of the battery when the battery is depleted is required in accordance with local laws and
regulations.
12) The handpiece must be repaired as necessary under the direction of the manufacturer.
13) Proper disposal of the handpiece when the handpiece is deemed non-functional is required in
accordance with local laws and regulations.
14) Removal of the battery is recommended when the handpiece is not to be used for an extended period of
time.
15) The acceptable temperature range for utilizing, storing and/or transporting the EndoActivator
-20°C to 45°C.
16) The handpiece should be stored away from strong electromagnetic equipment as it may affect handpiece
performance.
17) The handpiece should be stored away from portable and mobile RF communications equipment as it may
affect handpiece performance.
18) The handpiece should not be used adjacent to or stacked with other equipment. Additionally, it should be
checked for normal operating functions on a regular basis.
5) ADVERSE REACTIONS
None known.
BENENACDFUWEB / Rev.07 / 09-2019
System is only to be used by dental professionals.
®
System is comprised of the handpiece and Activator tips of various sizes. The system
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handpiece does not require calibration for normal use.
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System is required to prevent harm or hazard to the patient.
®
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handpiece may result in breaking the distal or proximal ends of
A0912
A0913 022-015 (Small)
A0913 022-025 (Medium)
A0913 022-035 (Large)
A0914
protective barrier sleeve placed
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System is
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