CMS RS01 Respiration Sleep Monitor SPO2/PR with analysis software

RS01 Sleep Apnea Monitoring Device – Home & Hospital Use

Product Description:
The  RS01 is a professional sleep apnea monitoring device designed for individuals suffering from Sleep Apnea-Hypopnea Syndrome (SAHS). It provides real-time SpO2 (blood oxygen saturation) and pulse rate (PR) monitoring, along with nasal airflow detection, making it suitable for both home and clinical use. With 12-hour continuous data recording and PC software analysis, it helps track sleep apnea events efficiently.

Key Features:

✔ SpO2 & Pulse Rate Monitoring – Displays real-time SpO2 (0%-100%) and PR (30-250 bpm) with pulse waveform.
✔ Nasal Airflow Detection – Measures breathing patterns (0-40 RPM) to detect apnea events.
✔ Audible & Visual Alarms – Alerts for low SpO2, finger detachment, or abnormal readings.
✔ Long Battery Life – Rechargeable lithium battery (3.7V) supports extended monitoring.
✔ Data Storage & Export – Stores multiple cases, transfers data via USB, and includes PC analysis software.
✔ User-Friendly Design – Lightweight (100g), compact (69×50×17.3mm), with real-time clock & auto power on/off.

Technical Specifications:

• SpO2 Accuracy: ±2% (70%-100% range)

• PR Accuracy: ±2 bpm or ±2%

• Resistance to Ambient Light: ±1% deviation under artificial/natural light.

• Operating Time: Up to 12 hours continuous recording.

• Power Supply: 3.7V lithium battery (included).

• Safety Compliance: Internally powered, Type BF applied part.

What’s Included:

• 1 × RS01 Sleep Monitor

• 1 × Power Adapter

• 1 × USB Data Cable

• 1 × Nasal Cannula

• 2 × SpO2 Probes (for different finger sizes)

• 1 × PC Software CD

• 1 × User Manual

Environment Conditions:

• Operating: 10°C ~ 40°C, ≤75% humidity

• Storage: -40°C ~ +55°C, ≤95% humidity

Ideal for:

• Home sleep apnea testing

• Hospital sleep studies

• Overnight SpO2 & breathing pattern tracking

Note: This device is for monitoring purposes only and should not replace professional medical diagnosis.

Order now and take control of your sleep health with the  RS01!

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The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item.

The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE &TUV of Europe.