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photoelectric ambulatory ECG workstation rac-2512
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photoelectric ambulatory ECG workstation rac-2512

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Retail price:
9426.0
$
Market price:
17281.0
$
Number:
RAC2512
Quantity
-
+
Stock:
0
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Temporarily out of stock
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Product description
parameter
Japan photoelectric ambulatory ECG workstation rac-2512
Product features
• compatible with 12 and 3 wave guides
• limb and chest electrode separation design to reduce lead interference
• dual security backup of host and SD card
• warning function of unanalyzed data
• breakpoint memory function
• multi user personalization
We could not find any corresponding parameters, please add them to the properties table

Japanese photoelectric dynamic ECG recording and analysis system
Bidding parameters
NO
Parameter requirements
Important parameter
one
◆ ECG recorder
one point one
The same machine is compatible with three or twelve lead ECG acquisition. A recorder can have both 12 lead recording mode and 3-lead recording mode.
yes
one point two
Three channel waveform display on the same screen of recorder
yes
one point three
Lead wire: physical separation design of chest electrode and limb electrode
yes
one point four
Input impedance ≥ 10m Ω
one point five
Common mode rejection ratio ≥ 90dB
one point six
Accuracy error of sensitivity < 10%
one point seven
Stability of sensitivity within 3% within 24h
one point eight
Internal noise ≤ 50 μ Vp-v
one point nine
Inter channel interference ≤ 0.2mvp-v
one point one zero
1 baseline fluctuation ≤ 0.1M V
one point one one
Frequency response 0.05Hz ~ 40Hz
one point one two
ECG recorder time constant adjustable: 0.3s or 3.2s
yes
one point one three
Weight ≤ 50g
yes
one point one four
Minimum resolution: 50 μ V
one point one five
With breakpoint memory function
yes
one point one six
Prompt for electrode falling off
one point one seven
It has the function of body movement detection to detect and record the movement of patients
yes
one point one eight
With dual security backup, the measurement data is saved in the memory card and backup memory at the same time
yes
one point one nine
At the same time, it is verified by aha/mit/nst/cu database analysis
yes
one point two zero
Configurable recording duration: 24 hours, 48 hours, 72 hours.
one point two one
The screen can display the remaining battery voltage value
yes
one point two two
With pacing detection function
two
◆ software analysis and editing
two point one
With multi-user personalized settings, software settings can be made according to different operating habits
two point two
With 24-hour histogram editing
two point three
With 24-hour heart rate trend chart
two point four
Simple, standard and detailed analysis standards can be set to meet different analysis standards for different patients.
two point five
It has the same screen event histogram editing function to realize the same screen event editing
two point six
Any interference interval can be selected and defined as non analysis interval to avoid the influence of interference waveform on diagnosis efficiency
two point seven
Chinese operation interface, compatible with 3-lead /12 lead data analysis.
two point eight
It provides the reset of analysis parameters. According to different clinical needs, it can set the scene of analysis function, so as to realize the flow of analysis.
two point nine
The heart beat superposition display window is provided, which can display the heart beats of the general template in line and compare them with each other, so as to make it clear at a glance of the heart beats that are incorrectly classified. At the same time, the editing function of reclassifying the heart beats in the heart beat superposition display window is provided.
two point one zero
Powerful pacemaker analysis function, applicable to AAI, VVI, DDD and other pacemakers, providing independent pacemaker analysis report.
two point one one
The independent 12 lead st scan analysis function provides independent analysis report, automatically analyzes the type of too high and low pressure, and provides the total load of myocardial ischemia.
three
◆ qualification requirements
three point one
The bidding product must have a third-party test report.
three point two
The bidding products must have product registration certificate.
three point three
The manufacturer shall have passed the ISO 9000 quality system certification.
three point four
The manufacturer shall have passed the ISO 13485 quality system certification.

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