Introducing our advanced Patient Monitor, a versatile device designed for monitoring adults, pediatrics, and neonates. This top-of-the-line monitor offers an array of essential functions including ECG, RESP, SpO2, PR, NIBP, and TEMP monitoring. Its user-friendly 8'' TFT color LCD touch screen ensures seamless navigation.
With PVI (Pleth Variability Index) feature and USB support for PDF file export, you can conveniently access detailed reports. This monitor is compatible with central station support and has Nurse Call functionality via wire or wireless network. The USB WIFI module allows for easy connectivity to CMS, while the USB data output enables simple viewing of data on your computer. Experience exceptional performance with its digital Spo2 sensor and from the human voice alarm system.With a storage capacity of 720 hours trend data and 12 hours of all waveforms, this monitor ensures comprehensive analysis. Additionally, it offers language options including English, French, German, Spanish, Portuguese, and more.
Invest in this Signs Monitor now for improved patient care and monitoring. 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.