GE Dash 3000 User manual

GE Healthcare
Bedside flexibility and adaptability
The Dash® monitoring family is a portable monitoring
system that is flexible and easy to use. Dash allows the
acuity of any bed to be modified to meet changing
patient needs.
Gold standard algorithms and technology
Dash monitors revolutionize patient care and assessment
by combining the most complete selection of gold standard
patient monitoring parameters with leading-edge
cardiac technology.
Enterprise networking
Hard-wired and wireless network connectivity – including
access to CIS, CVIS, PACS, RIS, HIS and more than 350 beds
without central station support – contributes to the Dash
monitors’ unprecedented ability to adapt to changing
patient acuity demands.
Dash 3000, 4000 & 5000
Flexible acuity monitoring

Product specifications
Display
Size Dash 3000 – 8.4 in., Dash 4000 – 10.4 in., Dash 5000 – 12.1 in.
Type Active-matrix color LCD
Resolution Dash 3000 and 4000: 640 by 480 dpi, Dash 5000: 800 by 600 dpi
Number of traces 7 (maximum)
Number of seconds/trace 4.9 at 25 mm/sec
Sweep speed 6.25, 12.5, 25 mm/sec (with erase bar)
Controls
TrimKnob® control
Five hard keys Standard Silence Alarm, Print, NBP Go/Stop, Zero All and Power On/Off. Dash 5000 adds
Trends, NBP Auto, Admit/Discharge, Standby and Main View
Remote control option Available
Alarms
Categories Patient status and system status
Priority 4 levels – Crisis, Warning, Advisory and Message
Notification Audible and visual
Setting Default and individual
Silencing 1 minute, current alarm only
Pause 5 minutes in Adult ICU mode, 3 minutes in Neonatal ICU mode and 5 minute,
15 minute, or permanent pause in OR mode
Volume Default 70 dB measured at 1 meter
Invasive blood pressure
Number of channels 1 to 4 (optional)
Transducer sites Arterial, femoral artery, pulmonary arterial, central venous, right atrial, left atrial,
intracranial and special
Transducer requirements Excitation voltage: 5 V dc ± 0.1%
Transducer output 5 µV/V/mmHg
Input specifications
Range -25 mmHg to 300 mmHg
Offset ± 150 mmHg
Output specifications
Frequency response dc to 50 Hz (-3 dB)
Zero balance range ± 150 mmHg
Zero balance accuracy ± 1 mmHg
Zero balance drift ± 1 mmHg over 24 hours
Accuracy ± 2% or ± 1 mmHg, whichever is greater
(exclusive of transducer)
Alarms User-selectable upper and lower limits for systolic, diastolic and mean pressures

ECG
Standard leads available I, II, III, V, aVR, aVL and aVF
3 leadwire I, II, or III
5 leadwire I, II, III, V, AVR, AVL, and AVF
10 leadwire I, II, III, AVR, AVL, AVF, VI, V2, V3, V4, V5 and V6
Leads analyzed simultaneously I, II, III and V (multi-lead mode)
Lead fail Identifies failed lead
Alarms User-selectable upper and lower heart rate limits
Input specifications
Voltage range ± 0.5 mV to ± 5 mV
Signal width 40 ms to 120 ms (Q to S)
Heart rate range 30 to 300 bpm
Input impedance Common mode > 10 MΩ at 50/60 Hz
Differential > 2.5 MΩ from dc to 60 Hz
Common mode rejection 90 dB minimum at 50 or 60 Hz
Output specifications
Impulse response For an impulse of 3 mV applied for 100 ms
Displacement following impulse < 0.1 mV
Slope following impulse < 0.3 mV/s
Frequency response Response of non-permanent displays is limited by resolution to 40 Hz (-3 dB)
@25 mm/s. Specified upper frequency limits may vary by ± 2 Hz.
Diagnostic mode 0.67 Hz (+0.4 dB) to 100 Hz (-3 dB)
For compliance with China 1.0 Hz (+0.4dB) to 75 Hz (-3 dB)
National Standard
Monitoring mode 0.67 (+0.4 dB) to 40 Hz (-3 dB)
Moderate mode 0.67 (+0.4 dB) to 25 Hz (-3 dB)
Maximum mode 5.0 Hz (-0.3 dB) to 25 Hz (-3 dB)
Noise < 30 µV (referred to input)
Pacemaker detection / rejection
Input voltage range ± 2 mV to ± 700 mV
Input pulse width 0.1 ms to 2 ms
Rise time 10 µs to 100 µs
Over/under shoot 2 mV (max)
Baseline drift < 0.5 mV per hour with a ± 700 mV, 2 ms
Pacemaker pulse Applied
Respiration
Measurement technique Impedance variation detection
Range 0-200 breaths per minute for variations of 1.0 – 10.0 Ω
Respiration rate 0-200 breaths per minute
Base impedance 100-1000 Ω at 52.6 kHz
Detection sensitivity 0.4 to 10 Ω variation
Waveform display bandwidth 0.1 to 1.8 Hz (-3 dB)
Alarms User-selectable upper and lower respiration rate limits, and user-selectable apnea limit

Temperature
Number of channels 2
Input specifications
Probe type YSI Series 400 or 700 (determined by input cable)
Temperature range 0°C to 45°C (32°F to 113°F)
Resolution ± 0.1°C
Output specifications
Parameters displayed T1, T2
Accuracy (independent of source) ± 0.1°C for YSI series 400; ± 0.3°C for YSI series 700 probes
Alarms User-selectable upper and lower limits for T1, T2
Cardiac output
Input specifications
Probe type In-line or bath probe
Catheter size 5F, 6F, 7F, 7.5F and 8F
Injectate volume 3, 5 or 10 cc
Output specifications
Parameters displayed Cardiac output, blood temperature, injectate temperature and trial number
Range
Cardiac output 0.2-15 (liters per minute)
Blood temperature 30-42°C
Injectate temperature 0-30°C
Accuracy
Cardiac output ± 5%
Blood temperature ± 0.2°C
Injectate temperature ± 0.3°C
Frequency response dc to 15 Hz ± 2 Hz
Pulse oximetry
Parameters monitored Arterial oxygen saturation (SpO2) and peripheral pulse rate (PPR)
SpO2 range Nellcor 1-100%; Masimo 30-100%; GE Ohmeda 30-100%
PPR range Nellcor 20-300 BPM; Masimo 25-240 BPM; GE Ohmeda 30-250
Accuracy Actual accuracy depends on probe. Please reference
manufacturer’s specifications.
Nellcor SpO2 ± 2 digits (70-100% SpO2)
Masimo SpO2 ± 2% Adults/Pediatric (70-100% SpO2)
GE Ohmeda SpO2 ± 2% (70-100% SpO2), SpO2 ± 3% Neonates, ≤ 69% unspecified
PPR ± 3 beats per minute
Alarms User-selectable upper and lower limits for SpO2 and PPR

DINAMAP non-invasive blood pressure
Technology DINAMAP® classic and SuperSTAT™ (SuperSTAT only
available with Masimo and Nellcor SpO2)
Measurement technique Oscillometric
Displayed parameters Systolic, diastolic and mean pressures, time of
last measurement
Measurement modes Adult ICU and OR modes; manual, auto and stat,
neonatal mode; manual and auto
Systolic
Adult 30-285 mmHg
Pediatric 30-235 mmHg
Neonate 30-140 mmHg
Map
Adult 20-260 mmHg
Pediatric 20-220 mmHg
Neonate 20-125 mmHg
Diastolic
Adult 10-220 mmHg
Pediatric 10-210 mmHg
Neonate 10-110 mmHg
Pulse rate, as displayed in tabular trends or 3 wave form display
Adult 30-200 bpm
Pediatric 30-200 bpm
Neonate 30-200 bpm
Other specifications
Overall system accuracy Meets or exceeds SP 10-1992 AAMI standards
Automatic cycle times 0-4 hours
Tubing length 12 feet adult, 8 feet neonatal
Automatic cuff deflation Cycle time exceeding 3 minutes (90 seconds neonatal),
French mode – Cycle time exceeding 2 minutes (60 seconds
neonatal), power off, or cuff pressure exceeds 294 mmHg
(± 6 mmHg) adult, 250 (± 5 mmHg) pediatric,
147 (± 3 mmHg) neonatal
Cuff sizes Thigh, large adult, adult, small adult, child, infant and
neonatal, sizes #5 - #1 and assorted long sizes
Alarms User-selectable upper and lower limits for systolic,
diastolic and mean pressures

CO2
Technology
Supports Novametrix CapnoStat (mainstream) and CapnoFlex LF (low-flow sidestream) CO2 technologies
Principle of operation Non-dispersive infrared (NDIR) single beam optics,
dual wavelength and no moving parts
Warm-up time 2 minutes warm-up time to meet accuracy specifications; waveform immediate
upon power up, calculated end tidal after two breaths
Cable length (mainstream) 8 foot (2.4 m)
Sample line length (low-flow sidestream) 7 foot (2.1 m)
Information displayed
Inspired and expired CO2 concentrations in %, mmHg or kPa; respiratory rate, continuous CO2 waveform
Measurement range (at 760 mmHg at an ambient temperature of 25°C)
0-100 mmHg, 0-13%, 0-12.5 kPa
PiCO2 /FiCO2 0-50 mmHg, 0-6.5%, 0-6.25 kPa
Respiration rate range Low-flow SS 0-150 breaths/min
Mainstream 0-120 breaths/min
Accuracy (at 760 mmHg at an ambient temperature of 25°C)
MS ±2 mmHg or 5%, whichever is greater
SS 0-40 mmHg ± 2 mmHg; 41-70 mmHg ± 5% of reading;
71-100 mmHg ± 8% of reading; all specifications ± 12%
of actual from 80-150 BrPM
Display resolution 1 mmHg
Rise time Less than 200 ms (low-flow sidestream); less than 60 ms
(mainstream adult reusable or SPU); less than 50 ms
(mainstream infant reusable or SPU)
Respiration rate accuracy ± 1 breath/min
Compensations
Automatic barometric pressure ± 25 mmHg from 530-785 mmHg
Operator-selectable O2/N2O compensation
Calibration
Mainstream No routine user calibration required. 15 second airway adapter zero performed
when changing to a different style of airway adapter.
Low-flow sidestream No routine user calibration required
Airway adapters and sample lines – mainstream (airway adapters)
Types Adult reusable (standard), adult disposable, infant
Deadspace Adult reusable/disposable < 5 cc
Infant disposable < 1 cc
Taper meets ISO 5356-1
Low-flow sidestream airway adapters
Types Adult reusable (standard), adult disposable, infant
Deadspace Adult reusable/disposable < 7.3 cc infant disposable < 1 cc
Adult, pediatric and infant Nasal CO2 and nasal CO2/O2
Adult and pediatric Nasal/oral CO2 and nasal/oral CO2/O2
Alarms
CO2 High inspired CO2; high/low expired CO2
Respiratory rate Adjustable high and low

Paper recorder
Method Thermal dot array
Horizontal resolution 480 dots/in. @25 mm/sec.
Vertical resolution 200 dots/in.
Number of waveform channels four
Paper width 50 mm (1.97 in.)
Paper length 30 m (100 ft.)
Paper speed 0.1, 0.5, 1, 5, 10, 12.5, 25 and 50 mm/sec. (± 2%)
Analog output
ECG
Gain 1 V/mV ± 10%
DC offset ± 100 mV (max)
Noise < 5 mV peak to peak 0-300 Hz
Frequency response Refer to frequency response section under ECG
Blood pressure
Gain 10 mV/mmHg ± 2%
DC offset ± 20 mV (max)
Noise < 5 mV peak to peak 0-300 Hz
Frequency response dc to 50 Hz-0/+2 Hz
Wireless LAN
Operating frequency 2.4 to 2.5 GHz
Transmit power 100 mW
Data rate (802.11) 1Mbps and 2Mbps per channel; (802.11b) 1, 2, 5.5, 11 Mbps
Radio technology Frequency-hopping spread spectrum
Communication protocol IEEE 802.11 or IEEEE 802.11b
UL 1950 Listed (ITE 9B97), CE Mark RF Standard
US/CAN FCC Part 15 Class B, RSS-210, Europe: ETSI EN 300 328, Japan: RCD STD-33R
Battery
Battery type Exchangeable Lithium-Ion
Maximum number of batteries 2
Voltage 11.1 V (nominal)
Capacity ≥ 3.45 Ah (varies with manufacturers)
Charge time Less than 4 hours each
Run time 4 to 5 hours
Battery life 500 cycles to 50% capacity
Environmental specifications
Power requirements 90-132 VAC 50/60 Hz 2.0A
190-264 VAC 50/60 Hz 1.0A
Power consumption 75 W (fully loaded)
Cooling Convection
Heat dissipation 240 Btu/hr. (max

GE imagination at work
GE Healthcare
P.O. Box 900, FIN-00031 GE, Finland
Tel. [phone] • Fax [phone]
www.gehealthcare.com
©2006 General Electric Company – All rights reserved.
GE and GE Monogram are trademarks of General Electric Company.
Masimo and SET are registered trademarks of Masimo Corporation.
Nellcor is a registered trademark of Nellcor Puritan Bennett, Inc.
Dash, TrimKnob, DINAMAP and SuperSTAT are registered
trademarks of General Electric Company.
GE Healthcare Oy., doing business as GE Healthcare.
Certification
UL2601-1 classified IEC 60601-1 certified
CE Marking for the 93/42/EEC UL Classified for CAN/CSA
Medical Device Directive C22.2 No. 601.1
2028034-002-2006.03-V2.0
Storage conditions
Do not exceed
Maximum 70°C (158°F) at 95% relative humidity
Minimum -40°C (-40°F)
CO2 sensor -30 to 65°C (-22 to 149°F)
Batteries -20 to 60°C (-4 to 140°F)
Physical specifications
Height Depth Width Weight*
Dash 5000 28.7 cm (11.3 in.) 23.9 cm (9.4 in.) 30.7 cm (12.2 in.) 6.4 kg (14 lbs.)
Dash 4000 27.4 cm (10.8 in.) 24.3 cm (9.6 in.) 29.3 cm (11.5 in.) 5.5 kg (12.2 lbs.)
Dash 3000 26 cm (10.25 in.) 20 cm (8 in.) 28 cm (11.0 in.) 5.2 kg (11.2 lbs.)
Operating conditions
Ambient temperature 0-40°C (32-104°F) (Nellcor 0-35°C (32-95°F))
While charging batteries 0-35°C (35-95°F)
CO2 sensor 10-40°C (50-104°F)
Relative humidity 5-95% @40°C
Vibration MIL-STD 810E, Method 514.4, Category 1
Altitude -273 m to 2,943 m (-896 to 9,655 ft.)
Warranty
Standard warranty is one year.
* Weight of product without batteries.