Vérin hydraulique de 30 tonnes, course de travail lourde de 50 mm à simple effet

  

Food and Drug Administration and state and local regulatory agencies. 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.