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FDA CE ETCO2 Capnograph Monitor Vital Signs Patient Monitor,7 parameter CMS8000

$ 421.34

Availability: 37 in stock
  • Monitor Parameters: Blood Pressure - NIBP
  • Brand: CONTEC
  • Item must be returned within: 60 Days
  • Screen Dimensions: 12.1"
  • Refund will be given as: Money Back
  • Condition: New
  • Restocking Fee: No
  • All returns accepted: Returns Accepted
  • Model: CMS8000
  • Return shipping will be paid by: Buyer
  • Country/Region of Manufacture: China
  • MPN: 69450401

    Description

    CONTEC CMS8000 Patient Monitor with 7-parameter including CO2
    Introduction
    The monitor has abundant functions that can be used for clinical monitoring with adult, pediatric and neonate. Users may select different parameter configuration according to different requirements. The monitor, power supplied by 100-240V~,50/60Hz,  adopts 12.1'' color TFT LCD displaying real-time date and waveform. It can synchronously display eight-channel waveform and full monitoring parameters equipped with an optional 48mm thermal recorder. The monitor can be connected to the central monitoring system via wire or wireless network to form a network monitoring system.
    This device can monitor such parameters as ECG, RESP, NIBP, SpO2, and dual-channel TEMP, etc. It integrates parameter measurement module, display and recorder in one device to form a compact and portable equipment. Its replaceable internal battery brings lot of convenient for patient moving.
    Features
    1)12.1'' TFT color LCD, multi-language interface(Simplified Chinese, Traditional Chinese, English, French, German, Turkish, Spanish, Portuguese, Italian, Dutch, Romanian, Russian, Kazakh, Polish, Czech).
    2)Fanless design, quiet, energy-saving and clean, which reduces the possibility of cross-infection.
    3)All-round monitor for adult, pediatric and neonate.
    4)With standard interface, oxygen graph, trend graph, big character interface and view bed, convenient to observe.
    5)Finish all operations by keys and knobs.
    6)Maximum 8-channel waveform synchronous display.
    7)Display 7-lead ECG waveform on one screen, cascade ECG waveform display
    8)Adopt digital SpO2 technology, anti-motion and anti-ambient light interference, and measurement can be performed under the circumstance of weak filling.
    9)Heart rate variability (HRV) analysis function
    10)NIBP measurement mode: Manual/AUTO/STAT, storage for 4800-group NIBP data.
    11)Review for 71 alarm events of all parameters and 60 arrhythmia alarm events.
    12)Drug concentration calculation and titration table functions.
    13)One-touch printing of trend graph
    14)Connect to Central Monitoring System by 3G, Wi-Fi or wired mode.
    15)AC/DC, built-in rechargeable lithium battery achieve uninterrupted monitoring.
    16)Anti-high frequency surgical unit, defibrillation-proof (special leads are necessary).
    Performance
    ▲ECG
    Lead mode: 3-lead or 5-lead
    Lead selection: I, II, III, aVR, aVL, aVF, V
    Waveform: 5-lead, dual-channel
    3-lead, single-channel
    Gain: 2.5mm/mV, 5.0mm/mV, 10mm/mV, 20mm/mV, 40mm/mV
    Scan speed: 12.5mm/s, 25 mm/s, 50 mm/s
    HR:
    Measurement and alarm range: 15~350 bpm
    Accuracy: ±1 % or ±1 bpm, whichever is greater
    Alarm accuracy: ± 2 bpm
    Resolution: 1 bpm
    ST-segment monitoring:
    Measurement and alarm range: -2.0 mV ~ +2.0 mV
    Accuracy: -0.8 mV~+0.8 mV  ±0.04 mV or ±10%, whichever is greater
    Other range: unspecified
    Arrhythmia analysis: ASYSTOLE, VFIB/VTAC, COUPLET, BIGEMINY, TRIGEMINY, R ON T, VT>2,
    PVC, TACHY, BRADY, MISSED BEATS, PNP, PNC
    Pacemaker: yes
    ▲RESP
    Method: R-F(RA-LL) Impedance
    Respiration rate:
    Measurement and alarm range: 0~150 rpm
    Resolution: 1 rpm
    Measurement accuracy: ±2 rpm
    Alarm accuracy: ±3 rpm
    Apnea alarm: 10~40s
    Scan speed: 6.25 mm/s, 12.5 mm/s, 25 mm/s
    ▲NIBP
    Method: Oscillometry
    Mode: Manual/AUTO/STAT
    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
    Resolution: 1 mmHg
    Cuff pressure accuracy: ±3 mmHg
    Measurement accuracy:
    Maximal mean deviation: ±5 mmHg
    Maximal standard deviation: 8 mmHg
    Over-pressure protection:
    Adult mode: 297±3 mmHg
    Pediatric mode: 240±3 mmHg
    Neonatal mode: 147±3 mmHg
    ▲SpO2
    Measurement and alarm range: 0 ~ 100%
    Resolution: 1%
    Measurement accuracy: 70%~100%: ±2%;
    0%~69%: unspecified
    ▲PR
    Measurement and alarm range: 30 ~ 250 bpm
    Measurement accuracy: ±2 bpm or ±2%, whichever is greater
    ▲TEMP
    Channel: dual-channel
    Measurement and alarm range: 0 ~ 50℃
    Resolution: 0.1 ℃
    Accuracy: ±0.1 ℃
    ▲EtCO2
    Method: Sidestream or Mainstream
    Measuring Range: 0~150mmHg
    Resolution:
    0~69 mmHg, 0.1 mmHg
    70~150 mmHg, 0.25 mmHg
    Accuracy:
    0~40 mm Hg ±2 mm Hg
    41~70 mm Hg ±5%
    71~100 mm Hg ±8%
    101~150 mm Hg ±10%
    AwRR Range: 2~150 rpm
    AwRR Accuracy: ±1BPM
    Apnea Alarm: Yes
    ▲IBP
    Channel: dual-channel
    Label: ART, PA, CVP, RAP, LAP, ICP, P1, P2
    Measuring and Alarm Range: -10~300 mmHg
    Resolution 1 mmHg
    Accuracy: ±2% or 1mmHg, whichever is greater
    ▲Power supply: 100-240V~, 50/60Hz
    ▲Safety classification: Class I, type CF defibrillation-proof applied part
    Accessories
    1)Adult fingertip SpO2 probe (5-pin)
    2)Adult NIBP cuff
    3)NIBP extension tube
    4)ECG lead cable
    5)ECG electrode
    6)Temperature probe
    7)Power cord
    8)User Manual
    9)CO2 tube
    Physical characteristic
    Dimension: 314 mm(L) × 145 mm(W) × 264 mm(H)
    Weight: 3.9 Kg
    FDA Declaration
    The following FDA Disclaimer is required for all eBay listing in Healthcare category and is
    included for REFERENCE: 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 the item is subject to FDA regulation, we will
    verify your status as an authorized purchaser of this item before shipping of the item.
    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
    International Buyers - Please Note:

    Import duties, taxes and charges are not included in the item price or shippingcharges. These charges are the buyer's responsibility.

    Please check with your country's customs office to determine what these additional costs will be prior to bidding/buying.
    Only English User Manual,Please contact us if you need other language manual.