at all times. Ultrasonic inserts tips that have been bent, reshaped
or otherwise damaged are susceptible to in-use breakage and
should be discarded and replaced immediately.
• Understand that Cavitron Ultrasonic Scaling Units and Cavitron
Ultrasonic Inserts are designed and tested for safety and efficacy
as a system. Use of any other brand ultrasonic insert with Cavitron
equipment has not been tested and may have a negative effect on
the safety and effectiveness of your Cavitron equipment and their
warranties. Please review the Warranty section before use.
• Understand that like bristles of a toothbrush, ultrasonic inserts
"wear" with use. Refer to the Efficiency Wear Indicators supplied
with your Cavitron Ultrasonic insert.
Adverse Reactions
None Known.
INSERT MARKING
Date Code
18218
30K FSI-PWR-1000 -AB 00005678
FDA'S UNIQUE DEVICE IDENTIFICATION (UDI)
+ D003807991/$$700005678/16D201803198
Unit Power Settings
• Slimline® 10S, L&R should only be used up to medium power.
• All other Cavitron Inserts may be used up to maximum power.
Operating Instructions
1.
Select the appropriate insert for the tooth or root to be
treated.
Decription
Tip Lot
Batch #
3