0407 - Specification NELLCOR Portable SpO2 Patient Monitoring System (PM10N)
0407 - Specification NELLCOR Portable SpO2 Patient Monitoring System (PM10N)
Enclosure Environmental
Weight 274 g (0.604 lb), including four batteries Transport and Storage Operating Conditions
Dimensions 70 mm W x 156 mm H x 32 mm D Temperature −20ºC to 70ºC 5ºC to 40ºC
(2.76 in. W x 6.14 in. H x 1.26 in. D) (−4ºF to 158ºF) (41ºF to 104ºF)
Display Altitude −390 to 5,574 m −390 to 5,574 m
(−1,280 to 18,288 ft.) (−1,280 to 18,288 ft.)
Screen size 88.9 mm (3.5 in.), measured diagonally
Relative humidity 15% to 95%
Screen type TFT LCD, white LED backlight, viewing cone of noncondensing
60º and optimal viewing distance of 1 meter
Resolution 320 x 480 pixels
Alarms
Trends
Categories Patient status and system status Types Tabular
Priorities Low, medium, and high Memory Saves a total of 80 hours of data events; saves date and
time, alarm conditions, pulse rate, and SpO2 measurements
Notification Audible and visual
Tabular One table for all parameters
Setting Default, institutional, and last setting format
Alarm volume level 49 to 89 decibels
Alarm system delay <10 seconds
Standards compliance
IEC 60601-1:2005+A1:2012, EN 60601-1:2006/AC:2010
Range and accuracy
IEC 60601-1:1998 +A1:1991 +A2:1995, EN 60601-1:1990 +A11:1993
Range Type Range Values +A12:1993 +A13:1996
Measurement Ranges IEC 60601-1-2:2007, EN60601-1-2:2007
SpO2 saturation range 1% to 100% IEC 60601-1-6:2010, EN 60601-1-6:2010 +A1:2013
Pulse rate range 20 to 250 beats per minute (bpm) IEC 60601-1-8:2006, EN 60601-1-8:2006 +A1:2012
Perfusion range 0.03% to 20% IEC 60601-1-11:2010, EN 60601-1-11:2010
Display sweep speed 6.25 mm/sec ISO 9919:2005, EN ISO 9919:2009
Measurement Accuracy ISO 80601-2-61:2011, EN ISO 80601-2-61:2011
Saturation CAN/CSA C22.2 No. 601.1 M90
Adult 70% to 100% ± 2 digits UL 60601-1: 1st edition
Adult and neonate low sat 60 to 80% ± 3 digits 802.11 B/G/N WLAN connectivity
Neonate 70 to 100% ± 2 digits
Low perfusion 70 to 100% ± 2 digits Equipment classifications
Adult and neonate with motion 70 to 100% ± 3 digits
Type of protection against Class I (internally powered)
Pulse rate electric shock
Adult and neonate 20 to 250 bpm ±3 digits Degree of protection against Type BF - applied part
electric shock
Low perfusion 20 to 250 bpm ±3 digits
Mode of operation Continuous
Adult and neonate with motion 20 to 250 bpm ±5 digits
Electromagnetic compatibility IEC 60601-1-2:2007
Ingress protection IP22: Protected against foreign
Electrical objects and moisture
Battery Four new lithium batteries with 3,000 mAh will typically provide Degree of safety Not suitable for use in the presence
20 hours of monitoring with no external communication, no of flammable anesthetics
audible alarm sound, and at an ambient temperature of 25°C
Type Lithium AA
Voltage 1.5 V x 4
Scope of Delivery:
- 1 Pcs Main Unit PM10N