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RSM-B
Bi-level Positive Airway Pressure (BiPAP)

With RESlex TM (Expiration Pressure Release)

RSM-B Series offers the ultimate in sleep therapy comfort. It combines auto adjusting pressure delivery with the breathe-by-breath pressure relief of RESlex TM for most natural sleep therapy. It also can provide non-invasive ventilation for patients with respiratory insufficiency in the hospital or home.


Professional precision

  • Innovative tracking technology ensures accurate and comfortable therapy.
  • Unique sensitivity setting offers individual therapy algorithm, makes every user get the most comfort.
  • RESlex TM performs better exhalation and compliance.
  • Inspiration trigger for auto start-up
  • Automatic stop after put off mask
  • Alarm when accidental power-off
  • In the time alert function when mask/ tubing off-line
  • Automatic leakage and altitude compensation ensure the therapy accuracy anywhere.

Ergonomic and powerful design

  • Integrated and knock-down designed InH2 TM heated humidifier
  • DC 12V powered and infrared controlled humidifier make user safe and comfortable.
  • Smart Heater automatic restarts after short term break.
  • Patented anti-countercurrent water tank
  • Unique Delay-off feature protects RESmart TM Auto from humidify hazard
  • Powerful embedded memory stores last night’s full raw data, 365 nights’ user Blog and more than 30 years’ therapy record.
  • User Blog direct output via portable thermal printer

Product Comparison:

Model

25

25A

25T

30T

Pressure (cm H2O)

4-25

4-25

4-25

4-30

Mode

CPAP, S

CPAP, S

CPAP, S,ST, T

CPAP, S,ST, T

Automatic Pressure

No

Yes

No

No

RESlex TM

Yes

Yes

Yes

Yes

Data Storage

Compliance, Leak

Compliance, Leak, Pressure, Fow, Snore, AHI, SNI

Compliance, Leak

Compliance, Leak

Altitude Compensation

Automatic

Automatic

Automatic

Automatic

Power Supply

100-240 VAC, 50/60Hz

100-240 VAC, 50/60Hz

100-240 VAC, 50/60Hz

100-240 VAC, 50/60Hz

Humidification

InH2 TM Heated Humidifier

InH2 TM Heated Humidifier

InH2 TM Heated Humidifier

InH2 TM Heated Humidifier


Technical Specifications (25/25A/25T):
Device Size
Dimensions: 220x194x112mm
313x194x112mm (with InH2 TM Heated Humidifier)
Weight: < 2kg

Environmental

Operating

Storage

Temperature

41 to 95°F (5° to 35° C)

-4 to 140°F (-20 to 60° C)

Relative Humidify

15 to 95% (non-condensing)

15 to 95% (non-condensing)

Atmospheric Pressure

77 to 101kPa (0 to 7500 ft)

N/A

 

Standards Compliance
This device is designed to conform to the following standards:

  • IEC 60601-1 General Requirements for Safety of Medical Electric Equipment
  • EN ISO 17510-1 Sleep Apnea Breathing Therapy Devices

Electrical

AC Power Consumption

100-240 VAC, 50/60 Hz, 1.0 A max.

Type of Protection Against Electric Shock

Class II Equipment

Degree of Protection Against Electric Shock

Type BF Applied Part

Mode of operation

Continuous

Electromagnetic Compatibility

The device meets the requirements of EN 60601-1-2, 2nd Edition

Fuses

There are no user-replaceable fuses



Pressure

Pressure Increments

4.0 to 25.0 cm H2O (in 0.5 cm H2O increments)

Pressure Stability

<10.0 cm H2O (±0.5 cm H2O)
≥10.0 cm H2O (±1.0 cm H2O)

Dynamic pressure accuracy is measured at the patient end of the circuit with a Whisper Swivel II and varying flow conditions. Measured in accordance with EN ISO 17510-1 @ 1/3, 2/3, and Pmax with BPM set to 10, 15 and 20BPM @ 20° C (±5°C), 50%RH (±5%), and an atmospheric pressure of 101.54 kPascals.

Maximum Flow

35LPM

Measured in accordance with En ISO 17510-1 @ Pmax.



Control Accuracy

Parameter

Range

Accuracy

IPAP

4 to 25 cmH2O

±0.5 cmH2O from static set point**

EPAP

4 to 25 cmH2O

±0.5 cmH2O from static set point**

Ramp Duration

0 to 60 minutes

± 10% of setting

Rise Time

0 to 3*

± 25%

*Rise time settings are adjustable by the patient and the provider from 0 (left) to 3. Rise time varies from 150msec to 400msec dependent on patient setting and the pressure differential from IPAP to EPAP. The rise time setting should be adjusted according to the patient comfort level.

** Measured at the patient end of the circuit with a Whisper Swivell II exhalation device and no patient flow.

Disposal
Dispose of the device in accordance with local regulations.

NOTE: Specifications subject to change without prior notice.


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