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Description:

 

Features:

1. The special wavelength and high density light speed catalyze whitening gel.

2. 6 powerful blue LED tubes emit a high intensive cold blue light and 4 powerful red LED tubes emit red light.

3. Special design, innocuous silica gel muzzle, make sure stopping intersectional infection.

4. The new model of power supply make sure steady power output and long- time continuous working even in some cities and places with mutative voltage.

5. Time display is suitable for human design, and could shows treatment time to help dentist master treating time and progress and reduce the waiting time of patient.

Specification:

1. Power supply: AC100-240V/ 50-60HZ

2. Power: 36W, 12V/3A

3. Light size: 30x80mm

4. Power density: >6000MW/CM2

5. Light timing: 0~20 mins

6. Power instability: <1%

7. Working method: time output & continuous working

8. Coupling: polyester mono wave

Package includes:

1*MAIN BODY

1* manual

 

FDA Disclaimer:


Statement:The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item.

This item has been cleaned and treated according to the manufacturer's instructions.

The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136606.

The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number:K132989

The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number:K180353

The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number:K141973

massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number:K161892 

Ultrasound ,Ultrasonic Treatment Device is certified with the US FDA 510(k) Number:K161892

This item has been cleaned and treated according to the manufacturer's instructions.

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