Category:

CONTEC08E Digital LED Upper Arm Blood Pressure Monitor NIBP Machine Adult cuff FDA

$24.99

20 in stock

Introduction

CONTEC08E is an LED screen Electronic Sphygmomanometer, with a simple interface, and one-key measurement,it can measure NIBP accurately, and NIBP records can be reviewed by the memory button and support voice broadcasting(optional). Moreover, the device is widely used in the family, clinic, and physical examination centers for a routine tests.

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. Moreover, LED color screen.Automatic power off when there is no operation for a long time,achieves saving power.

5. High-pressure prompt.

6. Additionally, it has Low battery and error information indication.

7. Optional units:mmHg and kPa

Performance

Measurement method: Oscillometry

The measurement mode: upper-arm type

And the measurement range: 0kPa(0mmHg)~ 39.6kPa(297mmHg)

Resolution: 0.133kPa(l mmHg)

Accuracy: ±0.4kPa(±3 mmHg)

PR measurement range: 40bpm~240bpm

The Inflation: automatic inflation by a force pump

Deflation:automatic multistep deflation

The 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 listings in the Healthcare category and is included for REFERENCE: The sale of this item may be subject to regulation by the U.S. Additionally, 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.