Lid options for DAC Universal D

Benefits

Why choose DAC Universal D?

Fully automatic reprocessing

Six instruments in approx. 15 minutes: Internal and external cleaning, lubrication (if needed) and disinfection2 of straight and contra-angle handpieces, turbines, ultrasonic / sonic handpieces and tips, nozzles of multifunctional syringes and powder jet devices as well as powder jet handpieces

Cost-effective and environmental friendly reprocessing

Low operating and consumption costs – no use of cleaning and disinfection chemicals, chemoindicators and only up to 800 ml water consumption per cycle. Low investment costs in instruments thanks to cooling at the end of the process and therefore quick return to service.

Ease of use

New design; touch display with intuitive user interface; guided maintenance workflow Check & Clean.

Legal certainty

Cleaning and disinfection process which can be validated and in accordance with EN ISO 15883-1 / -23.

“Reprocessed instruments in next to no time!”

Workflow

DAC Universal D cleans, lubricates (if necessary) and disinfects2 up to six straight and contra-angle handpieces and turbines and ultrasonic / sonic handpieces and tips, nozzles of multifunctional syringes and powder jet devices as well as powder jet handpieces in approx. 15  minutes – incl. cooling.

This workflow represents  a single cycle of the reprocessing of rotating instruments with the Program Blue Lid. With the Green Lid, the process is identical without the lubrication step.

Adapters

This is a selection of adapters for straight and contra-angle handpieces. To view all available adapters, please download the document "Ordering Information - Adapters" found in the Downloads Center. Please check the compatibility list for authorized ultrasonic / sonic handpieces and tips, nozzles of multifunctional syringes and powder jet devices as well as powder jet handpieces.

Downloads

Further downloads are provided within our Download Center.

121 KB

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Find out more about infection control systems from Dentsply Sirona.

1. Tested with temperature resistent paraviruses.

2. No sterilization 

3. Does not fully comply with all requirements. Details can be found in the instructions for use, chapter 3.7 "Supplementary information on compliance with EN ISO 15883-1/-2 and EN ISO 13060".