Nellcor PM1000N Bedside Respiratory Patient Monitoring System
The Nellcor Bedside Respiratory Patient Monitoring System, PM1000N incorporates the latest Nellcor digital signal processing and cardiac-based technology for accurate, reliable readings. Because Nellcor pulse oximetry is closely tied to patient physiology, it drives consistent performance during various challenging conditions, such as patient movement, noise, and low perfusion which can impede the assessment of patient respiratory status. The patient monitoring system is also cleared as a motion-tolerant bedside pulse oximeter that is compliant with ISO 80601--2--61.
With its intuitive, easy-to-read, graphical user interface and state-of-the-art color touch screen, this monitoring system provides clinicians with easy access to the critical information they need for patient care. The system provides continuous SpO₂, pulse rate and respiration rate monitoring, SatSeconds alarm management, and Saturation Pattern Detection (SPD) alert, so clinicians may detect respiratory complications earlier and, therefore, intervene sooner.
▣ Modular software, expandable parameters and easy upgrades to help ensure longterm functionality
▣ State-of-the-art, lightweight and versatile design
▣ Multiple connectivity options
▣ Includes Nellcor Respiration Rate Technology which delivers oxygen saturation (SpO₂), pulse rate, and respiration rate through a single finger sensor.
▣ Nellcor pulse oximetry with Oximax technology has accuracy claims of +/- 2% in the standard ranges of 70% to 100% saturation, and best-in-class LoSat accuracy claims of +/- 3% of 60% to 80%, enabling clinicians to accurately assess patients’ oxygen saturation.
▣ The speed of measuring oxygenation and displaying the value has been shown to be clinically important. In two published papers, clinical studies employed different sequences for sensor application and connection to the patient; Nellcor OxiMax technology responded fastest to changes in neonate patients.
▣ Covidien is the first and only company to receive FDA clearance for a motion-tolerant pulse oximeter portfolio that is also compliant with ISO 80601-2-61. Motion tolerant pulse oximetry is critical for ensuring patient safety because patient movement can thwart accurate readings and delay diagnosis of serious respiratory compromise.
Measurement Range: |
SpO₂: 1% to 100% |
Pulse rate: 20 to 250 beats per minute (bpm) |
Pulse amplitude: 0.03% to 20Accuracy |
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 |
Instrument | |
Power requirements: | 80-263 VAC, 47/63 Hz, 30 VA power |
Fuse rating: | Slow blow 1.5A 250V |
Battery | |
Type: Li-Ion | |
Battery capacity: | 6 hours under nominal load conditions |
Operating Temperature | |
Instrument:5°C to 40°C (41°F to 104°F) | |
Transport/Storage Temperature (in shipping carton): | -40°C to 70°C (-40°F to 160°F) |
Operating Humidity: | 15% to 95% noncondensing |
Operating Altitude: | -304.8 m to 4572 m (-1000 ft to 15,000 ft) |
Weight: 3.4kg (7.5 lbs) |
Size: 254 H x 165 W x 127 D (mm) |
10 H x 6.5 W x 5 D (in) |
Standards Compliance | |
EN ISO 80601-2-61 | 2011 |
EN IEC 60601-1 | 2005 |
EN IEC 60601-1-2 | 2007.03.01 3rd edition |
EN IEC 60601-1-2 | 2nd edition |
IEC 60601-1-8: 2006 and EN 60601-1-8:2007 | |
EN IEC 60601-1-9 | 2007 |
ISO 10993-1: | 2003 |
CAN/CSA C22.2 No. 60601-1:08 | |
WEEE 2002/96/EC | |
RoHS directive 2011/65/EU |
Type of protection against electric shock: | Class 1 (internally powered) |
Degree of protection against electric shock: | Type BF - Applied part |
Mode of operation: | Continuous |
Electromagnetic compatibility: | IEC 60601-1-2:2007 3rd edition |
Liquid ingress: | IPX1 |
Degree of safety: | Not suitable for use in the presence of flammable anesthetics |
Stores up to 48 hours of trend data readings that can be downloaded for analysis and archive |
Capability to connect to both wired and wireless LAN networks |
Capability to connect to Philips Vuelink Module and Nurse Call via wired serial port |
Capability to download trend data to PC |
Pulse Amplitude Indicator (16 segments) |
Plethysmographic waveform |
Real time numbers |
Real time trend data |
Multiple alarm conditions |
Up to 3 alarm conditions simultaneously |
SatSeconds Alarm Management |
OxiMax SPD Alert |
Battery Charging |
Clock |
Event Marker |
Histogram Display |
Clinical Log |
Neonatal Default Mode |
Audible and visual alarms for high/low saturation and pulse rate |
SatSeconds Alarm Management settings: 10,25,50 and 100, or OFF |
Saturation Pattern Detection sensitivity setting: 1,2,3 or OFF |
Pulse Rate Delay settings: 5, 10 or OFF |
Audible and visual warning indicators for low battery and sensor off |
Audible and visual sensor disconnect alarms |
Communication failure visual alarm |
Backup audible alarm |
Variable pitch beep tone for point-by-point changes in SpO2 |
User configurable sensor alarm prioritization |
GCX mounting adapter |
Interface cable |