Introducing our Signs Monitor, a versatile device designed for monitoring adults, children, and infants. With ECG, RESP, SpO2, PR, NIBP, and TEMP monitoring capabilities, this monitor provides accurate and reliable readings on its 8'' TFT color LCD touch screen. Featuring PVI (Pleth Variability Index) and USB support for PDF file export, this monitor also offers central station support and Nurse Call functionality through wired or wireless networks. With USB WIFI connectivity, data can easily be transferred to CMS for analysis. The monitor includes unique human voice alarms and supports 16 languages.
This product is perfect for hospitals, clinics, and home care settings. Package Include: 1×Patient Monitor 1×NIBP Cuff 1×SpO2 Probe 1×5 lead EKG?
Cable 1×Temperature Probe 1×NIBP extension cable 5×Electrode 1×User Manual. 5 Leads, I, II, III, AVR, AVL, AVF, V. 0.25,'0.5,'1,'2.
2.0 +2.0 mV. ±0.02mV or ±10%, which is greater. Impedance between RA-LL or RA-LA. 150 BrPM: ±2 BrPM or ±2%, the greater. 2 % for 70% 100%.Statement:The sale of this item may be subject to regulation by the U. 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. Ultrasound, Ultrasonic Treatment Device is certified with the US FDA 510(k) Number:K161892.