Item Brochure

Features and specifications
Performance
Measurement Range SpO
2
: 1% to 100%
Pulse rate 20 to 250 beats per minute (bpm)
Pulse amplitude 0.03% to 20%
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% ± 4 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
Electrical
Instrument
Power requirements 100 to 240 VAC, 50/60 Hz, 45 VA
Fuse rating Fast ‑acting 2 A 32VAC/DC,
Fast ‑acting 500 mA 32VAC/50DC
Battery
Type Lithium ion
Battery capacity Minimum of five hours using new, fully charged battery with
no alarms; optional 10‑hour battery
Environmental
Operating Temperature
Instrument 5 °C to 40 °C (41 °F to 104 °F)
Transport/Storage Temperature
(in shipping carton) ‑20 °C to 60 °C (‑4 °F to 140 °F)
Operating Humidity 15% to 93% noncondensing
Operating Altitude ‑170 m to 4877 m (‑557 ft to 16,000 ft)
Physical Characteristics
Weight 1.5 kg (3 lbs)
Size 82 H x 255 W x 155 D (mm), (3.23 H x 10.04 W x 6.10 D (in)
Equipment Compliance
Standards Compliance
• 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: 1
st
edition
• 802.11 B/G/N WLAN connectivity
Equipment Classifications
• Type of protection against electric shock: Class 2 (internally powered)
• Degree of protection against electric shock: Type BF – Applied part
• Mode of operation: Continuous
• Electromagnetic compatibility: IEC60601‑1‑2:2007
• Liquid ingress: IP 22
• Degree of safety: Not suitable for use in the presence of flammable anesthetics
Output
• Trend data download via wired or USB for archiving or data analysis
Display/Indicators
• Pulse amplitude indicator (eight segments)
• Visual indicators: Pulse search, audible alarms silenced or off, interference indicator,
battery charging, and SatSeconds alarm management clock, pleth wave form
Alarms
• SatSeconds alarm management
• Audible and Visual alarms for high/low saturation and pulse rate,
low battery, sensor off, and sensor disconnect
• Categories: Patient status and system status
• Priorities: Low, medium and high
• Notification: Audible and visual
• Setting: Default, institutional and last setting
• Alarm system delay: <10 s
Optional Accessories
• 10 and 15 hour battery
• Adapter plate
• GCX wall mount arm and channel
• GCX roll stand
• Carrying case
Available Modes
• Standard – Hospital, hospital ‑type facilities, and intra ‑hospital transport.
• Homecare – Simplified monitoring for use in the home by caregivers
• Sleep Study – Muted audible and visual queues to aid sleep studies
Connectivity
• Supports wired and USB trend data export to an external personal
computer for archiving or data analysis
• Nurse call capability
Simple set up and maintenance
The Nellcor
™
Bedside SpO
2
Patient Monitoring System meets medical electrical
equipment standards,
3
is RoHs compliant,
6
and enables hospital staff to set
institutional defaults, replace the battery, perform diagnostics to troubleshoot
performance issues, and perform on ‑site maintenance on the monitor.
1. Clinical Report, COVMOPR0384, Motion, LAMP ‑C (p/n 10099560)
2. Clinical Report, COVMOPR0250, LowSat Accuracy, LAMP ‑C (p/n 10099561)
3. 510(k) K123581 and certificate US‑23250‑M1‑UL
4. Saraswat A, Simionato L, Dawson J,etal. Determining the best method of Nellcor pulse oximeter sensor
application in neonates. Acta Paediatr. 2012;10195):484‑487.
5. O’Donnell CPF, Kamlin COF, Davis PG, Morley CJ. Obtaining pulse oximetry data in neonates: arandomized
crossover study of sensor application techniques. Arch Dis Child Fetal Neonatal Ed . 2005;90:F84‑F85.
6. Declaration of Conformity n°10138709 rev A ‑ Sept 24th, 2014
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