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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.
ThePowered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number：K132989
ThePowered Surgical Instrument / Hair Remove Deviceis certified with the US FDA 510(k) Number：K180353
ThePowered Surgical Instrument / Hair Remove Systemis certified with the US FDA 510(k) Number：K141973
massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA510(k) Number：K161892
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