SunTech CT40 Wireless Modular Vital Signs Monitor

SpO2 Specifications
FunctionMasimo
M-LNCS DCI Reusable Sensor
ChipOx
Saturation
Normal
(no motion)
70-100%Arms
± 2%
70-100%Arms
± 2%
Saturation
Motion
70-100%Arms
± 3%
N/A
Low
Perfusion
SpO2 +/-2%N/A
Pulse Heart
rate
± 3% BPM20-300 BPM: ±3
BPM
Pulse Heart
Rate
w/motion
± 3% BPM20-300 BPM: ±3
BPM

 

Temperature Specifications
FunctionTouchless IR
Thermometer
Covidien Electronic
Thermometer
Temperature AccuracyBody Temperature
(36-39°C) ± 0.2°C
Body Temperature
(34.0-35.9, 39.1-42.5°C)
± 0.3°C
Wide Temperature
(15-60°C) ± 2°C
Quick Mode
(Oral): ± 0.3°C
Std. Mode
(Aux/Rectal):
± 0.1°C
Direct Mode
± 0.1°C
Response
Time
< 2 seconds4 sec (quick mode);
10-15 sec.
(Axillary/Rectal);
60 sec.(direct mode)
Resolution0.1°C0.1°C

 

Blood Pressure Specifications
Range:Pressure: Diastolic: 20-200 mmHg (adult), 20-160 mmHg (pediatric).
Systolic: 40-260 mmHg (adult), 40-230 mmHg (pediatric)
Heart Rate: 30-220 BPM (beats per minute)
Accuracy (BP):Meets or exceeds ANSI/AAMI/ISO 81060-2:2013 standard for non-invasive
accuracy (±5mmHg mean error with 8mmHg standard deviation).
General Specifications
Conditions for Use:Operating: 10°C (50°F) to 40°C (104°F) 15 – 90% RH non-condensing –
70 kPa – 106 kPa. Operating the monitor in an environment at maximum
temperature can produce temperatures exceeding 41°C (41.6°C highest
recorded) on a patient-applied part. It is up to the operator to determine if
this temperature is too high based upon the condition of the patient and, if
so, to ensure the ambient temperature of the environment is 38°C or below
Storage:20°C (-4°F) to 55°C (149°F) 15 – 90% RH non-condensing – 50 kPa – 106 kPa.
Performance can be affected if used or stored outside the specified
temperature, humidity, or altitude listed in the ranges above.
Power:Internal power supply. Input: 100-240 VAC @ 1.5A max, 50-60 Hz. Output
+9VDC @ 5A IEC 320 type input connector.
Battery:Type: 7.2v, 6600mAh Internal Lithium-Ion battery
Run Time (full charge): ~20 hrs* / 200 BP cycles
Charge Time: ~6 hrs @ 23deg Celsius +/- 2deg
*Unit with BP, Temp, SpO2, Wi-Fi, barcode scanner
Calibration:The accuracy of cuff -pressure transducers/indicators should be verified bi-annually.
Safety Systems:Independent hardware over-pressure circuit and redundant software
overpressure algorithm to limit cuff pressure to less than 300 mmHg
(+20/-10mmHg). Independent hardware timing circuit and redundant
software timer algorithm to limit the duration of a blood pressure cycle to
less than 180 seconds.
Dimensions:Size (without thermometer option):
8” H x 6.75’’ W x 5.2’’ D or 215mm H x 190mm W x 140mm D
Standards:ANSI/AAMI ES60601-1:2005/(R)2012 and A1:2012, C1:2009/(R)2012 and
A2:2010/(R)2012, EN 60601-1:2006/A1:2013, IEC 60601-1-2: 2007 EMC, IEC
80601-2-30: 2013, ISO 80601-2-61: 2011, ISO 15223-1:2012, ISO 10993-1,
2009, ISO 10993-5, 2009, EN ISO 10993-10, 2010, ISO 81060-2:2013, EN
50419: 2006, EN ISO 14971:2009, CSA C22.2 No. 60601-1, EN ISO 81060-1:
2012, IEC 60601-1-6: 2013
Classifications:Equipment Classification: Class IIa per MDD, Class I (Electrical Shock),
Continuous mode of operation, CE
Ingress of liquid:Ingress Protection: IPX1: This device is protected against harmful effects of
dripping water per IEC 60529.