Medical Patient Monitor ICU CCU Vital Sign 6Parameter SpO2 PR NIBP ECG RESP TEMP

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Location: Monroe Township, New Jersey, United States
Ships to: US,
Item: 176330131155

eBay Description: Portable Multi-parameter Patient Monitor is adaptable to adult, pediatric and neonatal usage. It can monitor vital signals as ECG, Respiratory Rate, SpO2, NIBP, TEMP and IBP.It integrates parameter measuring modules, display and recorder in one device, featuring in compactness, lightweight and portability. Replaceable built-in battery facilitates transportation of patient. Features: 12″ high resolution color TFT LCD display. 6 Standard parameters:ECG, RESP, NIBP, SPO2, TEMP, PR. Can be arbitrarily set the alarm limit, automatic sound and light alarm. The back of the machine is designed with a storage box, which can put some accessories,convenient for doctors use. Drug solubility calculation function, Arrhythmia analysis function. Built-in lithium battery,AC and DC,can provide long-term monitoring after power failure. Widely used in the Department of internal medicine, Dental practices (both pediatric and adult), oral surgery centers surgery, operation room,obstetrics and Gynecology, pediatrics, emergency center,ICU,CCU. Specification: ECG Lead Mode:5 Leads ( R, L, F, N, C or RA, LA, LL, RL,V) Lead selection:I, II, III, avR, avL, avF, V, Waveform:2 ch Lead mode:3 Leads ( R, L, F or RA, LA, LL) Lead selection:I, II, III, Waveform:1 ch Gain:´2.5mm/mV, ´5.0mm/mV, ´10mm/mV, ´20mm/mV, auto HR and Alarm Range: Adult:15 ~ 300 bpm Neo/Ped:15 ~ 350 bpm Accuracy:± 1% or ± 1bpm,which great Resolution:1 bpm Sensitivity:> 200 (uV P-P) Differential Input Impedance:> 5 MΩ RESPARATION: Method:Impedance between R-F(RA-LL) Differential Input Impedance:>2.5 MΩ Measuring Impedance Range:0.3~5.0Ω Base line Impedance Range:0 – 2.5 KΩ Bandwidth:0.3 ~ 2.5 Hz Resp. Rate Measuring and Alarm Range Adult:0 ~ 120 rpm Neo/Ped:0 ~ 150 rpm Resolution:1 rpm Accuracy:±2 rpm Apean Alarm:10 ~ 40 S NIBP Method:Oscillometric Mode:Manual, Auto, STAT Measuring Interval in AUTO Mode 1, 2, 3, 4, 5, 10, 15, 30, 60, 90, 120, 180, 240,480 (Min) Measuring Period in STAT Mode:5 Min Pulse Rate Range:40 ~ 240 bpm Alarm Type:SYS, DIA, MEAN Measuring and alarm range: Adult Mode SYS :40 ~ 270 mmHg DIA :10 ~ 215 mmHg MEAN:20 ~ 235 mmHg Pediatric Mode SYS:40 ~ 200 mmHg DIA:10 ~ 150 mmHg MEAN:20 ~ 165 mmHg Neonatal Mode SYS:40 ~ 135 mmHg DIA:10 ~ 100 mmHg MEAN:20 ~ 110 mmHg Overpressure Protection Adult Mode:297±3 mmHg Pediatric Mode:240±3 mmHg Neonatal Mode:147±3 mmHg SpO2 Measuring Range:0 ~ 100 % Alarm Range:0 ~ 100 % Resolution:1 % Accuracy: 70% ~ 100% ±2 % 0% ~ 69% unspecified Actualization interval:about 1 Sec. Alarm Delay:10 Sec. Pulse Rate Measuring and Alarm Range:0~254bpm Resolution:1bpm Accuracy:±2bpm I.5TEMP measurement: Channel:1 Measuring and Alarm Range:0 ~ 50 °C Resolution:0.1°C Accuracy:±0.1°C Actualization interval:about 1 Sec. Average Time Constant:< 10 Sec. Package List: 1×Patient Monitor 1×EKG Lead wire 1×NIBP Cuff 1×NIBP Extension Cable 1×SpO2 Sensor 1×Temp Sensor 1×Ground Cable 5×Electrode 2×Fuse 1×User Manual(CD) FDA 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.Crystal-China-Beijing-86-15140779313 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

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