Portable Modular Patient Monitor 15 Inch ICU Quality Multi-Parameter ECG NIBP
$ 380.69
Description
Description: Introducing our 15 High-Resolution Color TFT LCD Portable Patient Monitor, designed for easy and convenient operation in various medical settings. This Multi-Parameter Signs Monitor features a modular design that allows flexible configuration to meet the specific needs of different departments. With support for up to 16 languages, it aids diverse user environments. Key functions include drug solubility calculations and arrhythmia analysis. It seamlessly connects to central monitoring systems via wired or wireless networks and includes a built-in lithium battery for reliable-term monitoring during power outages. Ideal for internal medicine, dental practices, surgery centers, obstetrics, pediatrics, emergency care, ICU, and CCU. Upgrade your patient monitoring today! Portable Multi-parameter Patient Monitor is adaptable to adult, pediatric and neonatal usage. It can monitor signals as ECG, Respiratory Rate, SpO2, NIBP, TEMP and IBP.Monitored date can be displayed, reviewed, stored and printed. Standard parameters :ECG, RESP, NIBP, SPO2, TEMP, PR. Optional :Dual IBP , CO2 , CSM module , Gas Specifications: 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 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% ~ ±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 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 1×User Manual FDA declaration : 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, we will verify your status as an authorized purchaser of this item before shipping of the item.(Seller Name: Sara;Country: China;City: Beijing;TEL.:86-15210656055). This item has been cleaned and treated according to the manufacturer's instructions. 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
