JPD-600P 12.1 LCD

Features:

1. 12.1 high-resolution color TFT LCD display, support plug-in large-screen CRT display

2.Standard Configure: FHR,TOCO,Fetal Movement, ECG, Spo2, NIBP, RESP, TEMP, Pulse Rate

3. Optional twins

4. Portable, convenient monitor

5. Built-in rechargeable battery, AC-DC power supply, without interruption Monitor

6.Dynamic save and display the Monitoring information within 48 hours

7.Both Use lonely or Connect with a Central Monitor network

8. Support the extension almost for 128 units central monitor system.

9. Quality “Sanyo” speaker take more clear and lound sound.

10. usual thermal paper,more economical.

Specification:

FHR:

Ultrasound Probe: 12pcs chip, Multi-wafer,wave-beam,high sensitive

Ultrasound frequency: 1MHz±5%

Ultrasound intensity: <3mW/cm2

FHR range: 30-240bpm

Resolution:1bpm

Accuracy:± 1bpm/±1%

TOCO:

TOCO range: 0-100 (relative unit)

Resolution:1

Non-linear error:≤±5%

Fetal Movement:

Button Hand Count( Automatic cumulative number of movements)

NIBP:

Measurement Units:mmHg/Kpa optional

Pressure protection: A double security protection software and hardware

Work Mode: Auto,Manual

Measurement intervals: 2-60 minutes set up

Survey: : Systolic blood pressure:60-240 mmHg
            Average Blood Pressure:40-200 mmHg
            Diastolic Blood Pressure: 30-180 mmHg

Resolution:1mmHg

Accuracy:±3mmHg

Pulse rate:40-240bpm

SPO2:

Range:70%-99%

Resolution:1%

Accuracy:±2 Effective digital

Pulse Rate:

Range:40-240bpm

ECG:

Range: 30-300bpm

Accuracy:±1bpm/±1%

Choice:I、II、 III、aVR、aVL、aVF、V

Scan Speed:12.5mm/s、25mm/s、50mm/s

Gain choice:x0.25、x0.5、x1、x2

Application:Diagnosis,Monitor,Surgery

RESP:

Range:1-99rpm

Resolution:1rpm

Accuracy:±2rpm

TEMP:

Range:26℃- 45℃

Resolution:0.1℃

Accuracy:±0.2%

Work environment:

Operation Temperature: 5℃- 40℃

Relative temperature:≤80%

Atmospheric pressure: (86-106)Kpa,32℃- 45℃:±0.1℃

Printer

50mm usual thermal paper,more economical

ARI-600G Digital 6 Channel ECG
 
Features of ARI-600G ECG:
--Simultaneously acquisition of 12-lead ECG data, IEC Class I, type CF safety standard
--Selectable four modes of leads
--Function of ECG parameters measurement and distinguish point printing under automatic mode
--LCD display of operation menu on ECG, ECG waveform, AMP menu and parameter setting
--Powerful filter for AC,EMG and DFT interference
--AC and DC power supply, rechargeable built-in battery in ECG
--High resolution and multiple print formats ensure best print quality of ECG waveforms
--Capability of the input & output for analog signal
--RS232
 
Specifications of ARI-600G ECG:
Input Circuit: Floating; protection against defibrillator effect of ECG
Lead: Standard 12 leads, European leads
Input Impedance: >50MΩ
Calibrating Voltage: 1mV±2%
Digital Sampling:12 bits (simultaneously acquisition of 12 leads ECG data)
DFT Filter Automatic Adjustment in ECG
Sensitivity: auto, 2.5, 5, 10, 20mm/mV
Recording System: Thermal-array
Paper Speed: 6.25,12.5, 25, 50mm/s(±3%)
Safety: Standard IEC class I, type CF
Power Supply AC: 96V~240V,50/60Hz±1Hz
DC: 14.4V~2000mAh rechargeable battery in ECG
Depolarization Voltage:±500mV

ARI-600G Digital 6 Channel ECG
 
Features of ARI-600G ECG:
--Simultaneously acquisition of 12-lead ECG data, IEC Class I, type CF safety standard
--Selectable four modes of leads
--Function of ECG parameters measurement and distinguish point printing under automatic mode
--LCD display of operation menu on ECG, ECG waveform, AMP menu and parameter setting
--Powerful filter for AC,EMG and DFT interference
--AC and DC power supply, rechargeable built-in battery in ECG
--High resolution and multiple print formats ensure best print quality of ECG waveforms
--Capability of the input & output for analog signal
--RS232
 
Specifications of ARI-600G ECG:
Input Circuit: Floating; protection against defibrillator effect of ECG
Lead: Standard 12 leads, European leads
Input Impedance: >50MΩ
Calibrating Voltage: 1mV±2%
Digital Sampling:12 bits (simultaneously acquisition of 12 leads ECG data)
DFT Filter Automatic Adjustment in ECG
Sensitivity: auto, 2.5, 5, 10, 20mm/mV
Recording System: Thermal-array
Paper Speed: 6.25,12.5, 25, 50mm/s(±3%)
Safety: Standard IEC class I, type CF
Power Supply AC: 96V~240V,50/60Hz±1Hz
DC: 14.4V~2000mAh rechargeable battery in ECG
Depolarization Voltage:±500mV

The HIV 1/2 Rapid Screen Test is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum or plasma. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.

 PRINCIPLE

It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens.

HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum or plasma. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, one or two  red colored bands will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, a red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.

The HIV 1/2 Rapid Screen Test is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum or plasma. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.

 PRINCIPLE

It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens.

HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum or plasma. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, one or two  red colored bands will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, a red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.

The one step Malaria PF/PV rapid test is designed as a simple, rapid, quolitative,and cost effective method for testing the presence of the plasmodium falciparum malaria in blood..

 For the rapid qualitative determination of Malaria P.falciparum specific histidine rich protein-2(Pf HRP-2)and malaria P.vivax specific lactate dehydrogenase (pLDH)in human blood as an aid in the diagnosis of Malaria infection.

The one step Malaria PF/PV rapid test is designed as a simple, rapid, quolitative,and cost effective method for testing the presence of the plasmodium falciparum malaria in blood..

 For the rapid qualitative determination of Malaria P.falciparum specific histidine rich protein-2(Pf HRP-2)and malaria P.vivax specific lactate dehydrogenase (pLDH)in human blood as an aid in the diagnosis of Malaria infection.

HCG Pregnancy test details:
1)CE marked
2)OEM can be offered
3)specialized manufacture and exporter with professional R&D team and workshop
4)format: strip,cassette and midstream
5)urine speciman
6)It can be sold in hospital,pharmacy,Clinic
7)The pen caps can be in different colors.

HCG Pregnancy test details:
1)CE marked
2)OEM can be offered
3)specialized manufacture and exporter with professional R&D team and workshop
4)format: strip,cassette and midstream
5)urine speciman
6)It can be sold in hospital,pharmacy,Clinic
7)The pen caps can be in different colors.

HCG Pregnancy test details:
1)CE marked
2)OEM can be offered
3)specialized manufacture and exporter with professional R&D team and workshop
4)format: strip,cassette and midstream
5)urine speciman
6)It can be sold in hospital,pharmacy,Clinic
7)The pen caps can be in different colors