CMS6000 ICU Patient Montior 7-parameter CO2 Monitor. The monitor has abundant monitoring functions and is used for monitoring of adult, pediatric and neonate. User may select different parameter configurations according to different requirements.It displays real-time data and waveform by 8'' TFT color LCD, and up to 8-channel waveform and all monitoring parameters can be displayed simultaneously. 48mm thermal printer is optional. In addition, it can be connected to the central monitoring system via wired/wireless network so as to form a network monitoring system. This device can monitor such parameters as ECG, RESP, SpO2, PR, NIBP and dual- channel TEMP, etc. It integrates parameter measurement module, display and recorder in one device to form a compact and portable equipment. At the same time, its built-in replaceable battery provides convenience for patient moving. Standard parameters: ECG, RESP, SpO2, PR, NIBP, dual-channel TEMP.
4NIBP Systolic pressure(SYS), Diastolic pressure(DIA), Mean pressure(MEAN). It has abundant functions, such as audible and visual alarm, trend data storage and output, NIBP measurement, alarm event marking and drug concentration calculation, etc. 18'' TFT color LCD, multi-language interface(Simplified Chinese, Traditional Chinese, English, French, German, Turkish, Spanish, Portuguese, Italian, Dutch, Romanian, Russian, Kazakhstan, Polish, Czech). 2Fanless design, quiet, energy-saving and clean, which reduces the possibility of cross-infection. 3All-round monitor for adult, pediatric and neonate.4With standard interface, OxyCRG, trend chard, big character interface and view bed, convenient to observe. 5Waveform, parameter color and location can be set optionally. 6Operation mode: keys and buttons. 7Display up to 8-channel waveform on one screen. 8Display 7-lead ECG waveform on one screen, and with ECG step function.
9Adopt digital SpO2 technology, anti-motion and anti-ambient light interference, and measurement can be performed under the circumstance of weak filling. 11NIBP measurement mode: Manual/AUTO/STAT, storage for 4800-group NIBP data.12Review for 71 alarm events of all parameters and 60 arrhythmia alarm events. 13Drug concentration calculation and titration table functions. 14Print trend table data with one-key. 15Connect to Central Monitoring System by 3G, WiFi or wired mode. 16AC/DC, built-in rechargeable lithium battery achieve uninterrupted monitoring. 17Anti-high frequency surgical unit, defibrillation-proof(special leads are necessary).
Lead mode: 3-lead or 5-lead. Lead selection: I, II, III, aVR, aVL, aVF, V. Gain: 2.5mm/mV, 5.0mm/mV, 10mm/mV, 20mm/mV, 40mm/mV.
Scan speed: 12.5mm/s, 25 mm/s, 50 mm/s. Measurement and alarm range: 15350bpm. Accuracy: ±1% or ±1bpm, whichever is greater. Alarm accuracy: ± 2 bpm.
Measurement and alarm range: -2.0mV+2.0mV. Accuracy: -0.8mV+0.8mV ±0.04mv or ±10%, whichever is greater. Arrhythmia analysis: ASYSTOLE, VFIB/VTAC, COUPLET, BIGEMINY, TRIGEMINY, R ON T, VT>2, PVC, TACHY, BRADY, MISSED BEATS, PNP, PNC. Measurement and alarm range: 0150rpm.
Scan speed: 6.25 mm/s, 12.5 mm/s, 25 mm/s. Measurement interval in AUTO mode: 1/2/3/4/5/10/15/30/60/90/120/240/480/960 minutes. Measurement period in STAT mode: 5 minutes.Measurement and alarm range: 10 270 mmHg. Cuff pressure accuracy: ±3 mmHg.
Maximal mean deviation: ±5 mmHg. Measurement and alarm range: 0 100%. Measurement and alarm range: 30 250 bpm.
Measurement accuracy: ±2 bpm or ±2%, whichever is greater. Measurement and alarm range: 0 50?Measurement range for CO2: 0 150mmHg. 0.1 mm Hg: 0 69 mm Hg. 0.25 mm Hg: 70 150 mm Hg. 0 40 mm Hg: ±2 mm Hg. 41 70 mm Hg: ±5%.
71 100 mm Hg: ±8%. 101 150 mm Hg: ±10%.Label: ART, PA, CVP, RAP, LAP, ICP, P1, P2. Measurement and alarm range: -10300 mm Hg. Accuracy: ±2% or 1mm Hg, whichever is greater. Safety classification: Class I, type CF defibrillation-proof applied part.
Adult fingertip SpO2 probe (5-pin). Dimension: 235 mm(L) × 141 mm(W) × 222 mm(H). Included for REFERENCE: The sale of this item may be subject to regulation by the U. Food and Drug Administration and state and local regulatory agencies.If the item is subject to FDA regulation, we will. The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG)with the code 197923. And certified by FDA of United States and CE, TUV of Europe. The Fingertip Pulse Oximeter that is FDA 510K Approved. Please leave your clear address, telephone, postal code / house number etc. International Buyers - Please Note. If you have a defective item, you want to return or discount. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Patient Monitors". The seller is "contec_medical_systems" and is located in this country: CN. This item can be shipped worldwide.