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Medical Patient Monitor ICU CCU Vital Sign 6Parameter SpO2 PR NIBP ECG RESP TEMP For Sale


Medical Patient Monitor ICU CCU Vital Sign 6Parameter SpO2 PR NIBP ECG RESP TEMP
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Medical Patient Monitor ICU CCU Vital Sign 6Parameter SpO2 PR NIBP ECG RESP TEMP:
$488.99

Description:

Portable Multi-parameterPatient Monitor is adaptable to adult, pediatric and neonatal usage. It can monitor vital signals as ECG, Respiratory Rate, SpO2, NIBP, TEMP and IBP.It integrates parameter measuring modules, display and recorder in one device, featuring in compactness, lightweight and portability. Replaceable built-in battery facilitates transportation of patient.

Features:

12\"high resolution color TFT LCD display.

6 Standard parameters:ECG, RESP, NIBP, SPO2, TEMP, PR.

Can be arbitrarily set the alarm limit, automatic sound and light alarm.

The back of the machine is designed with a storage box, which can put some accessories,convenientfor doctors use.

Drug solubility calculation function, Arrhythmia analysis function.

Built-in lithium battery,AC and DC,can provide long-term monitoring after power failure.

Widely used in the Department of internal medicine, Dental practices (both pediatric and adult), oral surgery centers surgery, operation room,obstetrics and Gynecology, pediatrics, emergency center,ICU,CCU.

Specification:

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

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 Protection

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% ~ 100% ±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 Time 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

2×Fuse

1×User Manual(CD)

FDAStatement: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 offer on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item.
This item has been cleaned and treated according to the manufacturer\'s Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136606.The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number:K132989The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number:K180353The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number:K141973massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number:K161892


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