Casmed, 01-02-0483, PPM3 Patient Monitor, Patient Monitors
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Sale Price: $4,895.00
Compared at: $5,395.00
You Save: $500.00
Product ID : CAS-01-02-0483
Manufacturer: Zoe Medical Inc.
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#0483: No CO2 Parameter Included
#0482: Add Masimo PhaseIn ISA CO2 Sidestream Analyzer (+$900.00)
No Strip Printer Included
#01-02-0807: Add External Strip Printer (+$550.00)

Overview

CASMED PPM 3 Patient Monitor

Description

PPM3 Patient Monitor with ECG, MAXNiBP NIBP, & Nellcor Compatible SpO2. Masimo PhaseIn ISA CO2 Sidestream option available. Includes patient cables and startup accessories. Battery Type Lithium-Ion Rechargeable, Discharging Time 5 hours. Monitor warranty is two years. Order mounting options separately.


PPM 3 Patient Monitor:

The foundation of the system is the Personal Patient Monitor™ (PPM3). The PPM3 connects to a patient via non-invasive sensors and monitors the patient's vital signs. The PPM3 contains proprietary hardware and software needed to perform complex data acquisition and signal processing tasks, allowing it to produce accurate and reliable measurements of physiological parameters including 3-lead ECG, pulse oximetry, blood pressure, respiration and temperature.

The PPM3 provides an easy to use knob and a simple set of control keys for user interaction, and a high brightness color display for enhanced visibility. The PPM3 also contains built-in hardware for networking and printing. The PPM3 raises a new standard of convenience, economy, and ease of use in patient monitors.

Weighing only 4.5 pounds, including a 5 hour lithium ion battery, the PPM3 is one of the lightest full-featured vital signs monitors in the world. Also, at less than 2.5 inches thin, the PPM3 fits easily into even the most crowded bedside environments.

PPM 3 Screen Shots



Main Screen - uncluttered layout with large, bright, easy to read numbers




Parameter setup menus - easily accessed directly from main screen



Alarm setup - all alarm limits and settings can also be set from one menu




Trends - vital sign measurements can be saved on demand or at preset intervals, and printed




Waveforms - easily change the configuration of which waveforms to see where




Setups - easily save a setup that you like, restore to a previously saved one, or restore factory defaults




Standby - enter standby mode, initiate transport, or discharge patient from the bedside



Biomedical - via password menu, select settings to control alarm system behavior


CASMED PPM3 Technical Data

General

Dimensions 11.3”W x 7.2”H x 2.4”D (288 mm x 182 mm x 60 mm)
Weight 4.5 lb (2.0 g), 5.0 lb w/ Oridion Microstream® CO2 (2.3 kg)
Finish PC/ABS
Power Requirements 100 – 240 VAC, 1.2 A max Mains Frequency Range 50 – 60 Hz Power Consumption 12W nominal, 30W (when charging battery)
Standards Conformance
IEC 60601-1:2005 (General Safety)
AAMI ES60601-1:2005 (General Safety)
CSA C22.2#60601-1:2008 (General Safety)
IEC 60601-1-2:2007 (Class B) (EMC)
IEC 60601-1-4:2000 (General Safety)
IEC 60601-1-8:2006 (Alarms)
IEC 60601-2-27:2011 (ECG Monitoring)
AAMI SP10:2002/A1:2003 (Non-Invasive Blood Pressure)
ISO 80601-2-30:2009 (Non-Invasive Blood Pressure)
IEC 60601-2-34:2011 (Invasive Blood Pressure)
ISO 80601-2-55:2011 (CO2 Respiratory Gas Monitoring)
ISO 80601-2-56:2009 (Temperature)
ISO 80601-2-61:2011 (SpO2) IEC 62366:2007 (Usability)
IEC 62304:2006 (Software)
Patient Risk Current
(IEC 60601-1)
Electromedical Apparatus with Isolated Patient Connection.

Meets the following limits:
Enclosure Risk Current < 100 μA
Patient-applied Risk Current < 10 μA
Patient Isolation Risk Current < 50 μA
Earth Risk Current < 500 μA
Type of Protection (Electrical) Class I
Degree of Protection (Electrical) Type CF, Defibrillation-proof
Degree of Protection (Water) Ordinary Equipment (IPX1)
Disinfecting Method Per the instructions in the Cleaning chapter
Degree of Safety (Flammable
Anesthetic Mixture)
Not suitable for use in the presence of a Flammable Anesthetic
Mixture
Mode of Operation Continuous

PPM3 Device Markings

Local Area Network interface
Interface for MPC central station
Interface for Other Medical Devices – Reserved for future use
Recorder interface
ECG 3 and 5 wire ECG connector
SpO2 Pulse Oximetry connector
NBP Non-Invasive Blood Pressure connector

Battery

Type Lithium-Ion Rechargeable
Discharging Time 4 hours (minimum)
Charging Time 5 hours
Charging Method Battery is charged while monitor is connected to AC main

Environmental

Cooling Convection (no fan)
Operating Temperature 32 to 104 °F (0 to 40 °C)
Storage Temperature -4 to 140 °F (-20 to 60 °C)
Operating Humidity 15% to 90% non-condensing
Storage Humidity 15% to 95% non-condensing
Operating Altitude 0 to 15,000’ (0 to 4572 m)
Storage Altitude 0 to 40,000’ (0 to 12,192 m)
Alarm Signal Sound Pressure 45 to 80 dB(A)

Display

Type Active Matrix LCD
Size 8.4 inches (diagonal)
Matrix 800 x 600 pixels
Number of Waveform Channels Up to 5
Sweep Speed 6.25, 12.5, 25 mm/s
Display Mode Eraser Bar

ECG

Accessories 3-lead cable, 5-lead cable
Input Connector 7-pin connector
Displayable Leads
3-lead cable: I, II, III, AVL, AVR, AVF
5-lead cable: I, II, III, AVL, AVR, AVF, V
HR Resolution 1 bpm (beats per minute)
Measurement Range 15 to 300 bpm
Measurement Accuracy ±2 bpm or ±1%, whichever is greater
Response Time
Per IEC 60601-2-27, change from 80 to 120 bpm: < 7 seconds
Per IEC 60601-2-27, change from 80 to 40 bpm: < 11 seconds
Report Interval 1 second
HR Averaging Scheme
Average of the 10 most recent, valid R-R intervals, discarding the shortest and longest interval
Time To Alarm - Tachycardia
IEC 60601-2-27, ECG Complex B1: < 10 sec (5 sec typical)
IEC 60601-2-27, ECG Complex B2: < 10 sec (9 sec typical)
Notch Filter Frequency 50Hz, 60 Hz, Off
Filter Bandwidth
Monitor Mode: 0.67 Hz to 40 Hz (-3 dB)
Diagnostic Mode: 0.05 to 40 Hz (-3 dB)
Dynamic Range AC ±5 mV, per IEC 60601-2-27
Dynamic Range DC ±300 mV, per IEC 60601-2-27
Electrode Impedance >2.5 MOhm , per IEC 60601-2-27
Defibrillation Protection Complies with IEC 60601-2-27
Pacer Pulse Detection Lead II, I and V
Pacer Pulse Rejection
Rejects all pulses of amplitude ±2mV to ±700mV and duration 0.1 to 2 ms, per IEC 60601-2-27, Clause 201.12.1.101.13 Tall T-Wave Rejection Rejects T-Waves less than or equal to 120% of a 1mV QRS and a Q-T interval of 350 ms, per IEC 60601-2-27, Clause 201.12.1.101.17
HR Response to Irregular Rhythm
IEC 60601-2-27, ECG Complex A1: HR is 80 bpm
IEC 60601-2-27, ECG Complex A2: HR is 65 bpm
IEC 60601-2-27, ECG Complex A3: HR is 120 bpm
IEC 60601-2-27, ECG Complex A4: HR is 91 bpm
Active Noise Suppression RL drive (< 5 μA)
Pulse Tone Yes

Respiration

Method Impedance Pneumography
Input Connector Same as ECG
Sensing Lead II
RR Resolution 1 bpm (breaths per minute)
Measurement Range 0 to 120 bpm
Measurement Accuracy ±3 bpm
Measurement Sensitivity 0.25 ohms (minimum)
Report Interval 1 second
Bandwidth 0.17 to 3.3 Hz (-3dB)
Impedance Measuring Current 40 μA @ 28 kHz square wave across Lead II

Pulse Oximetry

Method
Absorption – Spectrophotometric (dual wavelength) (Functional oxygen saturation of arterial hemoglobin)
Input Connector 9-pin connector SpO2 / PR Resolution
SpO2: 1 O2% PR: 1 bpm (beat per minute) Measurement Range
SpO2: 20 to 100% PR: 30 to 240 bpm
Measurement Accuracy
SpO2: from 70 to 100%: ±2% (O2%), < 70%: unspecified
PR: ± 3 bpm
Measurement Test Method Comparison versus co-oximeter, per ISO 80601-2-61
Report Interval 1 second. Numeric values held < 30 seconds
Pulse Tone Yes (pulse tone pitch tied to SpO2 parameter value)
Alarm Signal Generation Delay < 0.5 sec

Non-Invasive Blood Pressure

Method Oscillometric
Input Connector Single Lumen Hose (Quick-Disconnect fitting)
Cuff Infant, Child, Small Adult, Adult, Large Adult
Derived Parameters Systolic, Mean, Diastolic
Resolution 1 mmHg
Measurement Range
Systolic: 30 to 250 mmHg
Mean: 20 to 230 mmHg
Diastolic: 10 to 210 mmHg
Measurement Accuracy Complies with AAMI SP10
Transducer Accuracy ± 3 mmHg
Pulse Rate Range 30 to 240 bpm
Pulse Rate Accuracy ± 5% or ± 2 bpm, whichever is greater
Update Interval Upon measurement completion
Measurement Time 30 seconds (typical) < 135 seconds (maximum)
Initial Cuff Pressure 160 mmHg (user-selectable)
Repeated Cuff Pressure Previous systolic + 40 mmHg
Static Cuff Pressure Accuracy ± 3 mmHg
Overpressure Cutoff 290 ± 3 mmHg (normal means), 300 ± 10 mmHg (back-up)
Measurement Modes Single Measurement or Auto (Interval) Measurement
Auto Measurement Settings Off, 3, 5, 10, 15, 30, 60, 120 minutes

Masimo ISATM CO2 / Capnography

Method Sidestream (Non-dispersive IR)
Units mmHg
Parameters ETCO2, FICO2, RRc
CO2 Measurement Range ETCO2 & FICO2: 0 to 150 mmHg
CO2 Measurement Accuracy
As measured with dry single gases: 0 to 15 vol%: ±(0.2 vol% + 2% of reading) 15 to 25 vol%: unspecified
CO2 Resolution 1 mmHg
RRc (Resp. Rate) Measurement
Range 0 to 150 ± 1 bpm
RRc Resolution 1 bpm
Barometric Pressure Range 525 to 1200 hPa
Barometric Pressure
Compensation
Automatic
Report Interval Per breath
Flow Rate 50 ± 10 sml/min
Warm-up Time Required to
Meet Accuracy Specifications < 10 seconds (concentrations reported and full accuracy)
Total System Response Time < 3 seconds (with 2m Nomoline sampling line)
Drift of Measurement Accuracy Complies with EN ISO 21647:2004 standard
Measurement Accuracy for Gas Mixture Complies with EN ISO 21647:2004 standard
Measurement Accuracy in the Presence of Interfering Gases Complies with EN ISO 21647:2004 standard


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