The Nellcor portable SpO₂ patient monitoring system, PM10N, is a convenient, handheld monitor that is ideal for spot-checks or continuous monitoring in various healthcare and home use settings. Its ergonomic shape and simple design make it intuitive to use and simple to operate. Wherever you need accurate, reliable SpO₂ measurements, count on the Nellcor portable SpO₂ pulse oximeter to meet the challenge.
The monitoring system includes a vivid 3-inch color LCD screen, and connectivity to analytic tools and patient management systems. It is compatible with the entire line of Nellcor sensors with OxiMax technology and offers a robust monitoring feature set including SpO₂, pulse rate, SatSeconds alarm management, pleth waveform, blip bar and tabular trend information.
The monitor incorporates Nellcor digital signal processing technology to deliver accurate, reliable SpO₂ and pulse rate values even during low perfusion and signal interference, including patient motion.
Nellcor Portable SpO₂ Patient Monitoring System, PM10N Features
▣ Small, lightweight, ergonomic handheld monitor for continuous and spot-check pulse oximetry monitoring
▣ Supports a robust data set, including real-time SpO₂ and PR values, SatSeconds alarm management, pleth waveform, blip bar and tabular trend data
▣ Supports standard and home-care modes for use in hospital, hospital-type facilities, transport, mobile environments and home-care environments
▣ Supports Sleep Study Mode, which enables the clinician to dim the LCD display and silence alarms to prevent disruption of patients’ sleep
▣ Nellcor advanced signal processing technology delivers reliable operation even in difficult monitoring conditions
▣ LoSat expanded accuracy range (60% to 100% SpO₂) when used with Nellcor adhesive sensors with OxiMax technology
▣ Compatible with the complete line of Nellcor single-patient-use, reusable and specialty sensors with OxiMax technology
▣ 80 hours of data storage capability
▣ Supports data export to an external personal computer for data analysis and printing functions
Weight: | 274 g (0.604 lbs), including four batteries |
Dimensions: | 70 mm W x 156 mm H x 32 mm D |
(2.76 in W x 6.14 in H x 1.26 in D) |
Display: | |
Screen size: | 88.9 mm (3.5 in), measured diagonally |
Screen type: | TFT LCD, white LED backlight, viewing cone of 60º and optimal viewing distance of 1 meter |
Resolution: | 320 x 480 pixels |
Alarms: | |
Categories: | Patient status and system status |
Priorities: | Low, medium and high |
Notification: | Audible and visual |
Setting: | Default, institutional and last setting |
Alarm volume level: | 49 to 89 dB |
Alarm system delay: | <10s |
Range Type: | Range Values |
Measurement Ranges: | |
SpO₂ saturation range: | 1% to 100% |
Pulse rate range: | 20 to 250 beats per minute (bpm) |
Perfusion range: | 0.03% to 20% |
Display sweep speed: | 6.25 mm/sec |
Measurement Accuracy: | |
Saturation: | |
Adult: | 70% to 100% ±2 digits |
Adult and neonate low sat: | 60 to 80% ±3 digits |
Neonate: | 70 to 100% ±2 digits |
Low perfusion: | 70 to 100% ±2 digits |
Adult and neonate with motion: | 70 to 100% ±3 digits |
Pulse rate: | |
Adult and neonate: | 20 to 250 bpm ±3 digits |
Low perfusion: | 20 to 250 bpm ±3 digits |
Adult and neonate with motion: | 20 to 250 bpm ±5 digits |
Battery: | Four new lithium batteries with 3,000 mAh will typically provide 20 hours of monitoring with no external communication, no audible alarm sound and at an ambient temperature of 25° C. |
Type: | Lithium AA |
Voltage: | 1.5V x 4 |
Transport and Storage: | Operating Conditions: | |
Temperature: | -20 ºC to 70 ºC, | 5 ºC to 40 ºC |
(-4 ºF to 158 ºF) | (41 ºF to 104 ºF) | |
Altitude: | -390 to 5,574 m, | -390 to 5,574 m |
(-1,280 to 18,288 ft.) | (-1,280 to 18,288 ft.) | |
Relative humidity: | 15% to 95% non-condensing |
Types: | Tabular |
Memory: | Saves total 80 hours data events. Saves date and time, alarm conditions, pulse rate and SpO₂ measurements |
Tabular format: | One table for all parameters |
IEC 60601-1:2005+A1:2012, EN 60601-1:2006/AC:2010 |
IEC 60601-1:1998 + A1:1991 +A2:1995, EN 60601-1:1990 +A11:1993 +A12:1993 +A13:1996 |
IEC 60601-1-2:2007, EN60601-1-2:2007 |
IEC 60601-1-6:2010, EN 60601-1-6:2010 +A1:2013 |
IEC 60601-1-8:2006, EN 60601-1-8:2006 +A1:2012 |
IEC 60601-1-11:2010, EN 60601-1-11:2010 |
ISO 9919:2005, EN ISO 9919:2009 |
ISO 80601-2-61:2011, EN ISO 80601-2-61:2011 |
CAN/CSA C22.2 No. 601.1 M90 |
UL 60601-1: 1st edition |
802.11 B/G/N WLAN connectivity |
Type of protection against electric shock: | Class I (internally powered) |
Degree of protection against electric shock: | Type BF - applied part |
Mode of operation: | Continuous |
Electromagnetic compatibility: | IEC 60601-1-2:2007 |
Ingress protection: | IP22: Protected against foreign objects and moisture |
Degree of safety: | Not suitable for use in the presence of flammable anesthetics |