Covidien Nellcor PM100N Bedside SpO2 Patient Monitor + New DS-100A Sensor & Trunk Cable
Covidien / Nellcor PM100N Bedside SpO₂ Patient Monitoring System
Compact bedside pulse oximetry monitor supplied with a brand-new Nellcor DS-100A reusable adult SpO₂ sensor and brand-new Nellcor trunk/interface cable. The monitor itself is in used condition and is shown powered on in the photographs.
Package includes:
- 1 × Covidien / Nellcor PM100N bedside SpO₂ monitor – used condition
- 1 × Nellcor DS-100A reusable adult finger SpO₂ sensor – brand-new condition
- 1 × Nellcor trunk/interface cable – brand-new condition
Key specifications:
- Continuous SpO₂ and pulse-rate monitoring
- SpO₂ measurement range: 1% to 100%
- Pulse-rate range: 20 to 250 bpm
- Pulse-amplitude range: 0.03% to 20%
- Displays real-time SpO₂, pulse rate, plethysmographic waveform and pulse amplitude
- Nellcor SatSeconds™ alarm management
- Adult, paediatric and neonatal modes
- Standard, Homecare and Sleep Study modes
- Colour display with on-screen help
- Up to 96 hours of trend memory
- Audible and visual alarms for high/low SpO₂ and pulse rate, low battery, sensor-off and sensor-disconnect conditions
- Wired / USB trend-data export capability
- Nurse-call capability
- Power requirement: 100–240 VAC, 50/60 Hz, 45 VA
- Lithium-ion battery system; standard 8-hour and optional 16-hour battery configurations were offered by the manufacturer
- Approx. dimensions: 82 × 255 × 155 mm
- Approx. weight: 1.5 kg
- IP22 enclosure rating
Condition: Monitor is used with normal cosmetic signs of previous use. It powers on and the display is shown operating in the photographs. The Nellcor DS-100A sensor and Nellcor trunk/interface cable are in brand-new condition.
Compatibility: Designed for use with compatible Nellcor OxiMax™ SpO₂ sensors and accessories. The included DS-100A is a reusable adult finger sensor. Buyer should confirm suitability for the intended patient population and application before use.
Price: £299 + shipping
Availability: 1 set available
DISCLAIMER: Used professional medical equipment. The buyer/end user is responsible for confirming compatibility and suitability and for carrying out any required inspection, electrical safety testing, calibration and functional verification before clinical use. The monitoring system should not be used as the sole basis for diagnosis or therapy.