C50 Parameters
C50 Parameters
C50 Parameters
Product Specifications
1) Monitor Type
Classified by Type
Electric shock protection
Externally powered Class-I equipment; continuous operation equipment
type
Defibrillation-proof
defibrillation resistant equipment with internal power supply.
applied parts
Electric shock protection Equipment with CF applied part (ECG, C.O. and IBP monitoring part) and
level BF applied parts (all other monitoring parts).
IP grade IPX1
Work mode Continuous operation equipment
IEC 60601-1 IEC 60601-1-8 IEC 60601-2-27 EN 1060-3 IEC 80601-2-30
Safety standards
IEC60601-2-34 IEC60601-2-49 ISO 80601-2-56 ISO 80601-2-61
2) Environmental Specifications
Item Specification
Ambient
Working 5℃~40℃
temperature
conditions
RH ≤93%
Product specification
Barometric
700hPa~1060hPa
pressure
Please protect the monitor against violent impact, vibration, rain and snow in
Transport transport. The monitor should be Transported in a well-ventilated room without corrosive
conditions gas (ambient temperature: -20 ℃ ~60 ℃ ; RH: ≤93%; Barometric pressure:
700hPa~1060hPa).
The monitor should be packed and stored in a well-ventilated room without corrosive gas
Storage conditions (ambient temperature: -20 ℃ ~60 ℃ ; RH: ≤93%; Barometric pressure:
700hPa~1060hPa).
3) Power Supply
Item Specification
AC input voltage 100~240V
AC input frequency 50Hz/60Hz
Power supply Powered either by built-in battery or external AC.
Input power 60VA
C80/50: Standard: 11.1V/2200mAh rechargeable lithium-ion battery, supplying power
for at least 2 consecutive hours in normal use once fully charged.
Optional: 11.1V 4400mAh rechargeable lithium-ion battery, supplying power
Built-in battery
for at least 4 consecutive hours in normal use once fully charged.
C86: Standard: 11.1V 4400mAh rechargeable lithium-ion battery, supplying power for
at least 4 consecutive hours in normal use once fully charged.
11.1V 4400mAh: At least 4 hours from depletion to 90% charge in normal use.
Charge time
11.1V/2200mA: At least 2 hours from depletion to 90% charge in normal use.
Defibrillation output +5V defibrillation synchronization signal during 100ms
Synchronization Max delay: ≤35ms; Pulse width: 100ms±10; Up/Down time≤1ms
4) General Specifications
Item Specification
Dimension C50: About 291.7mm×250 mm×146.5mm
Weight C50: About 3.3kg(with battery)
LCD specification C50: Size: 10.4 Inch
Pixel :800×600
5) ECG Specifications
Item Specification
Applicable standards: IEC 60601-2-27.
12-lead (R, L, F, N, C1, C2, C3, C4, C5, C6 or RA, LA, LL, RL, V1, V2, V3, V4,
Lead mode
V5, V6)
Method of leads I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6
Waveform 2 -channel
Lead mode 5-lead (R, L, F, N, C; or RA, LA, LL, RL, V)
Method of leads I, II, III, aVR, aVL, aVF, V
Product specification
Waveform 2 -channel
Lead mode 3-lead ( R, L, F; or RA, LA, LL)
Method of leads I, II, III
Waveform 1-channel
Load 1V, power frequency, differential-mode AC voltage for 10s without damage
Overload protection
(p-v)
Resp, lead
AC waveform:
disconnection
Current :<0.1µA;
detection and active
Frequency 64kHz, ±10%
noise control
Auto identify the type of ECG leads.
Amplitude (p-v RTI) 0.5mV~5mV
Width (adult) 70ms~120ms
Width (neonate/child) 40ms~120ms
QRS wave amplitude
and interval a) with amplitude (p-v RTI) not exceeding 0.15mV
Not respond to the (except in neonate/child mode); or
signals: b) with 10ms width (except in neonate/child mode) in
case of 1mV amplitude.
Triggering threshold
200µV (lead II)
level
Power frequency
>100µV(p-v)
voltage tolerance
Triangular wave
4mV
amplitude (p-v RTI)
QRS wave amplitude
0.5 mV
Drift tolerance (p-v RTI)
QRS wave width 100ms
QRS wave recurrence
80bpm
frequency
Adult 15~300bpm
HR measurement Neonate/child 15~350bpm
range and error ±1% or ±1bpm in both 3-lead, 5-lead and 12-lead mode,
Error
whichever is greater.
Adult 15bpm~300bpm
Alarm limit range
neonate/child 15bpm~350bpm
Alarm limit
±1bpm
resolution
Alarm limit error ±1bpm
Alarm start time for
asystole and high/low <10s
HR
Input signal amplitude ±5mV
Input dynamic range Rate (RTI) 320mV/s
DC offset voltage -300~+300mV
Product specification
Hysteresis effect of
≤0.5mm
15mm offset
Calibration voltage ±5% error at 1mV
Common mode
<1mV (p-v RTI)
rejection
Recovery time after
3s
reset
Baseline control and Drift rate in 10s 10µV/s
stability Baseline drift in 1h ≤500µV
Baseline drift at
≤50µV/℃
working temperature
Amplitude: ±2mV~±700mV; width: 0.1ms~2.0ms; if overshoot < 0.05ɑ p, settling
Non-overshoot
time < 5µs; start time, end time, rise time and fall time of pulse: ≤ 100µs; start time
pacemaker pulse
of pulse: 40ms or earlier before the start time of QRS wave; there is an identical
inhibition
pulse 150ms~250ms before the above pacemaker pulse.
Inhibition of
pacemaker pulse
Minimum input slew rate: 320mV/s RTI
detector on quick
ECG signals
Amplitude: ±2MV~±700MV; width:
Pacemaker pulse 0.5MS~2MS; maximum rise time:
≥0.2mV
display capability 100µS; the ECG display when the
pacemaker pulse appears at 100/min.
Measurement range -2.0mV-+2.0mV (-20.0 mm~+20.0 mm)
ST segment
-0.8mV~+0.8mV: ±0.02mV or ±10%, whichever is greater.
measurement Measurement error
Other ranges: not defined.
STalarm limit range -2.0mV-+2.0mV
ST alarm limit error ±0.1mV
Resolution 0.01mV (0.1mm)
Asystole, ventricular fibrillation (VFIB)/ventricular tachycardia (VTAC),
PVCs/min, R on T, VT>2, couplet, PVC, bigeminy, trigeminy, tachycardia
(TACHY),bradycardia (BRADY), supraventricular tachycardia (SVT), extreme
Arrhythmia types tachycardia, extreme bradycardia, missed beats, multiform PVC (multi. PVCs),
VTAC, nonsustained VT (nonsus. VTAC), ventricular rhythm, heart pause,
pause/min, irregular rhythm (irr. rhythm), ventricular bradycardia, atrial fibrillation,
pacemaker not captured (PNC), pacemaker not paced (PNP).
Leakage current <10uA
Electrosurgical
interference HR change caused by interference: ≤±10%
inhibition
Cut mode: 300W
ESU protection Condense mode: 100W
Recovery time: ≤10s
HR Calculation
Product specification
Adult 0rpm~120rpm
RR alarm limit range and
Neonate/c
error 0rpm~150rpm
hild
Error ±1rpm
Adult: 110s、15s、20s、25s、30s、35s、40s、45s、50s、
No breath alarm limit Range 55s、1min
range and error Child/neonate: 10s、15s、20s、25s、30s、35s、40s
Error ±5s
No breath alarm delay 10s、15s、20s、25s、30s、35s、40s、45s、50s、55s、1min、Off
The Monitor will display the relevant alarm message when the HR is identical
CVA identification
with the RR.
7) SpO2 Specifications
Item Specification
Display range 0%~100%
Display resolution 1%
Product specification
8) PR Specifications
Item Specification
Comen SpO2 sensor:
Measurement range: 20bpm~254bpm; resolution: 1bpm; measurement
error: ±2bpm.
Masimo SpO2 sensor:
Measurement range: 25bpm~240bpm; resolution: 1bpm; measurement
error: ±3bpm (in non-motion state) or ±5bpm (in motion state).
9) Temp Specifications
Item Specification
Measurement range and Measurement range 0℃~50℃
accuracy Measurement error ±0.1℃(excluding the sensor error)
Temp alarm limit range Alarm limit range 0℃~50.0℃
and error Alarm limit error ±0.1℃
Resolution 0.1C
Number of channels 2
Operating mode Direct mode
Transient response No greater than 40 seconds
Error ±5s
No breathalarm
10s、15s、20s、25s、30s、35s、40s、45s、50s、55s、1min、Off
delay
Respironics/Nmed/Palconn EtCO2
Respironics/Nmed/Palconn EtCO2 sensor (mainstream)
sensor (sidestream)
CO2 0~150mmHg 0~150mmHg
measurement 0%~19.7% 0%~19.7%
range (0~20.0kPa) (0~20.0kPa)
0~69mmHg: 0.1mmHg 0~69mmHg: 0.1mmHg
CO2 resolution
70~150mmHg: 0.25mmHg 70~150mmHg: 0.25mmHg
0~40mmHg: ±2mmHg 0~40mmHg: ±2mmHg
41~70mmHg: ±5%×reading 41~70mmHg: ±5%×reading
CO2 accuracy
71~100mmHg: ±8%×reading 71~100mmHg: ±8%×reading
101~150mmHg: ±10%×reading 101~150mmHg: ±10%×reading
CO2 alarm limit
0~150mmHg 0~150mmHg
range
CO2 alarm
±0.1kPa or ±1mmHg ±0.1kPa or ±1mmHg
resolution
awRR
measurement 0~150rpm 0~150rpm
range
awRR
measurement ±1rpm ±1rpm
accuracy
awRR alarm
0~150rpm 0~150rpm
limit range
awRR alarm
1rmp 1rmp
resolution
Adult:10s、15s、20s、25s、30s、35s、
No breath alarm 40s、45s、50s、55s、1min
Range
limit range and Child/neonate: 10s 、 15s 、 20s 、 25s 、
error 30s、35s、40s
Error ±5s
No breathalarm
10s、15s、20s、25s、30s、35s、40s、45s、50s、55s、1min、Off
delay
Diastolic
1.3-28.7kPa (10-215mmHg)
pressure
Mean
2.7-31.3kPa (20-235mmHg)
pressure
Systolic
5.3-26.7kPa (40-200mmHg)
pressure
Measurement range Diastolic
1.3-20kPa (10-150mmHg)
(child) pressure
Mean
2.7-22kPa (20-165mmHg)
pressure
Systolic
5.3-18kPa (40-135mmHg)
pressure
Measurement range Diastolic
1.3-13.3kPa (10-100mmHg)
(neonate) pressure
Mean
2.7-14.7kPa (20-110mmHg)
pressure
Measurement Maximum average deviation: ±5mmHg (±0.667kPa);
accuracy maximum standard deviation: ±8mmHg (±1.067kPa).
Adult mode 297mmHg
Overpressure protection Child mode 240mmHg
range and tolerance Neonate mode 147mmHg
Tolerance ±3mmHg
Systolic
5.3kPa~36kPa (40mmHg~270mmHg)
pressure
Diastolic
Adult 1.3kPa~28.7kPa (10 mmHg~215mmHg)
pressure
Mean
2.7kPa~31.3kPa (20mmHg~235mmHg)
pressure
Systolic
5.3kPa~26.7kPa (40mmHg~200mmHg)
pressure
Diastolic
Alarm limit range and Child 1.3kPa~20kPa (10mmHg~150mmHg)
pressure
error
Mean
2.7kPa~22kPa (20mmHg~165mmHg)
pressure
Systolic
5.3kPa~18kPa (40mmHg~135mmHg)
pressure
Neonat
Diastolic
e 1.3kPa~13.3kPa (10 mmHg~100mmHg)
pressure
Mean
2.7kPa~14.7kPa (20mmHg~110mmHg)
pressure
Error ±0.1kPa or ±1mmHg, whichever is greater.
Manual, auto (cyclic) or continual (not applicable to neonates)
1/2/2.5/3/4/5/10/15/30/60/90/120/180/240/480/720m
NIBP measurement mode Interval for auto mode
in
Continual 5min
Product specification
Initialpressurerange(mm
Adult:80~280;Child:80~210;Neonate:60~140
Hg)
P2 -50mmHg~300mmHg
P3 -50mmHg~300mmHg
P4 -50mmHg~300mmHg
LV 0mmHg~300mmHg
AO 0mmHg~300mmHg
UAP 0mmHg~300mmHg
BAP 0mmHg~300mmHg
FAP 0mmHg~300mmHg
UVP -10mmHg~40mmHg
IAP -10mmHg~40mmHg
IBP alarm error ±0.1kPa or ±1mmHg
Sensitivity: 5V/V/mmHg
Pressure sensor
Impedance range: 300~3000Ω
Pressure zero calibration Each channel should feature a pressure zero calibration function, with an
accuracy of ± 1mmHg or ± 0.1kPa.)
14) AG Specifications
Item Specification
The AG module complies with ISO 80601-2-55.
AG measurement method Infrared radiation absorption characteristics
The following accuracy standards are applicable to a dry gas under 22±5°C and
1013±40hPa.
0%~15% ±(0.2kPa+reading×2%)
CO2
15%~25% Not defined.
N2O 0~100 % ±(2kPa+reading×2%)
0~8 % ±(0.15 %+reading×5%)
Hal, Enf, Iso
8~25 % Not defined.
0~10 % ±(0.15 %+reading×5%)
Sev
10~25 % Not defined.
0~22 % ±(0.15 %+reading×5%)
Des
22~25 % Not defined.
O2 0~100 % ±(1%+reading×2%)
RR 0~254rpm ±1rpm
CO2: 1mmHg
AG resolution
awRR: 1rpm
AG gas name
CO2, O2, N2O, one of the five anesthetic gases (Enf, Iso, Sev, Hal or Des)
EtHal/EtEnf/EtIs
0%~25% ±0.1%
o/EtSev/EtDes
FiHal/FiEnf/FiIs
0%~25% ±0.1%
o/FiSev/FiDes
Item Specification
Specifications of ISATM (AG) Sidestream Gas Analyzer
Product specification
Measurement
Infrared gas measurement
method
For adult: 10s, 15s, 20s, 25s, 30s, 35s, 40s ,45s, 50s, 55s or 1min;
[No Breaths Range
For pediatric and neonate: 20s, 25s, 30s, 35s or 40s
Timeout]
Error ±5s
[No Breath
10s, 15s, 20s, 25s, 30s, 35s, 40s, 45s, 50s, 55s, 1min or Off
Alm Delay]
General Specifications
Ultra-small low-flow sidestream gas analyzer, with integrated micro-pump, zeroing valve
Description
and flow controller.
Working
ISA AX+: 0~50°C (32~122°F); ISA OR+: 5~50°C (41~122°F)
conditions
Storage
-40~70°C (-40~158°F)
conditions
RH <4kPa H2O (non-condensing) 95% RH, 30°C
Barometric
52.5~120kPa (4572m)
pressure
Water
Sampling tube: patented dehydration tube
treatment
Data Output
Fi/Et value CO2, O2, N2O, five anesthetic gases (Hal, Enf, Iso, Sev, Des)
Waveform Display up to 4 gas concentration waveforms at a time
Diagnostic
Barometric pressure
parameter
Gas Analyzer
ISA sensor 2~9-channel NDIR gas analyzer (measurement range: 4~10µm)
Compensation CO2 broadening effect
No calibration is required. The Monitor will auto perform zeroing when powered on and
Calibration
perform auto zeroing every 24h (ISACO2) or 8h (ISA AX+/OR+) subsequently.
Preheating time ISA CO2: <10s; ISA OR+/AX+: < 20s
Gas
Rise time CO2: ≤250ms; N2O: ≤ 350ms; anesthetic gases: ≤ 350ms; O2: ≤450ms
Overall system
<3s (2m sampling tube)
response time
Respiration
Self-adaptive threshold (minimum CO2 concentration change: 1 vol%)
detection
RR 0-150 breaths/min
Anesthetic gas Threshold of main anesthetic gases (ISA OR+/AX+): 0.15 vol%. The concentration of
threshold any identified anesthetic gas will be reported, even if it is lower than 0.15 vol%.
Paramete
Alarm Limit Step Size
r
BIS alarm limit
BIS 0~100 1
HR: 40~250bpm
Measurement range SV: 5~250mL
C.O.:1.4~15L/min
SV: not defined.
Measurement accuracy HR: ±2bpm.
C.O: no defined.
SV: 0.1ml
Resolution HR: 1bpm
C.O: 0.1L/min
Alarm Limit Resolution
Upper limit: (lower limit +
0.1)~15.0L/min/m2
C.I. 0.1L/min/m2
ICG alarm limit and Lower limit: 1.4~(upper limit -
resolution 0.1)L/min/m2
Upper limit: (lower limit +
TFC 1)~150/KΩ 1KΩ
Lower limit: 5~(upper limit - 1)KΩ
Number of waveforms 3
Item Specification
The alarm system complies with IEC 60601-1-8.