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CONTEC Digital LED Upper Arm Blood Pressure Monitor NIBP Machine Adult cuff FDA

$ 10.02

Availability: 34 in stock
  • Bundle Listing: Yes
  • Brand: CONTEC
  • Operation: Automatic
  • Mounting: Portable
  • Country/Region of Manufacture: China
  • Model: CONTEC08E
  • Intended Use/Discipline: Family Medicine
  • Body Location: Arm
  • MPN: 69450401
  • Cuff Size: Adult
  • Condition: New
  • Monitor Type: Arm-Type Digital

    Description

    FDA Digital blood pressure Monitor Adult BP cuff CONTEC08E
    Introduction
    CONTEC08E is an LED screen Electronic Sphygmomanometer,simple interface and one-key measurement,it can measure NIBP accurately,NIBP records can be reviewed by the memory button and support voice broad casting(optional). The device is widely used in family,clinic and physical-examination center for routine test.
    1.Features
    2.Small volume,one-key measurement,easy to operate,big font in displaying,simple and easy to understand the displayed contents.
    3.Start measuring manually,record each measurement data,and store up to 199 groups of data.
    4.LED color screen.Automatic power off when there is no operation for a long time,achieves saving power.
    5.High pressure prompt.
    6.Low battery and error information indication.
    7.Optional units:mmHg and kPa
    Performance
    Measurement method:Oscillometry
    Measurement mode:upper-arm type
    Measurement range:0kPa(0mmHg)~ 39.6kPa(297mmHg)
    Resolution:0.133kPa(l mmHg)
    Accuracy:±0.4kPa(±3 mmHg)
    PR measurement range:40bpm~240bpm
    Inflation:automatic inflation by force pump
    Deflation:automatic multistep deflation
    Display:LED large color screen
    Power:Four"AA"batteries/5V Power adapter
    Safety character:Class II Type BF
    Physical characteristic
    Dimension:130mm(L)×110mm(W)×80mm(H)
    Accessories
    Cuff for adult
    User manual
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    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