WESTERN SURGICAL
Specialist of sleep diagnosis and therapy

Specialist of sleep diagnosis and therapy

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Specialist of sleep diagnosis and therapy

  • Technical Specifications
  • Device size
  • Dimension : 220*194*112mm  313*194*112mm (with inH2 heated humidifier)
  • Weight : < 2.2kg  <3 kg (with inH2 heated humidifier)

 Environmental

     operating   Transport and storage
 Temperature               5 to 30c   -20 to 55c
 Relative hurnicity
 < 80% Non-condensing 
 < 93% Non-condensing 
 Atmospheric Pressure
 860 to 1060 hpa
  500 to 1060 hpa

STANDARDS COMPLIANCE

  • IEC 60601-1 general requirements for safety of medical electrical equipment
  • IEC 60601-1-2 electromagnetic compatibility
  • ISO 17510-1 sleep apnoea breaking therapy
  • ISO 8185 general requirements for humidification system

ELECTRICAL

                   AC power consumption : 100-240v AC, 50/60Hz, Max 95VA Type of protection against electric shock : class 2 equipment degree of protection against electric shock : Type BF applied part degree of protection against ingress of water : Device : Drip proof, IPX1 mode of operation : continuous

MODE COMPARISON 

 Product Model
Pressure
Function
Auto Pressure
 Sleepsmart BPAP 25
  4.25cm H2O 
  S, CPAP
 No
 Sleepsmart BPAP 25A
  4.25cm H2O    S,CPAP
 available
 Sleepsmart BPAP 25 T
  4.25cm H2O    S,CPAP, T,S/T
 No
 Sleepsmart BPAP 30 T
  4.30cm H2O    S,CPAP,T,S/T
 No

  • IPAP :  4 to 30 cmH2O +-1 cmH2O**
  • EPAP : 4 to 25 cmH2o +-1 cmH2O**
  • CPAP : 4 to 20 cmH2o +-1 cmH2O**
  • Respiratiory Rate : 3 to 30 BPM, greater of +-1 BPM or +-10% of the setting (when measured over a 4 minutes period)
  • E/I Rate : 1-4
  • Max. inspiration time : 3.0 seconds
  • Ramp. duration : 0 to 45 minutes +-10% of the setting
  • Rise time : 1 to 3*** +- 25%*****
  • Limited to 20 cmH2o when using auto feature in s mode
  • Dynamic pressure accuracy is +-1 cmH2O measured at the patient end of the circuit with a vio nasal mask and varying flow conditions.
  • Static pressure accuracy is +-0.5 cmH2O measured at the patient end of the circuit with a vio nasal mask and no patient flow.
  • The range of values corresponds to tenths of seconds (e.g.., a setting of 4 indicates a rise time of 0.4 seconds)
  • Measured at the patient end of circuit with a vio nasal mask exhalation device and no patient flow.

DISPOSAL

Dispose of the device in accordance with local regulations.

NOTE :

Specifications subject to change without prior notice