Datascope – Spectrum OR

SOLICITAR COTIZACIÓN

SOLICITAR COTIZACIÓN

  • Built-in, vivid 12.1-inch display with auto-adjustablelarge numerics and waveforms for optimal visibility.
  • Includes the standard functions you need for perianesthesia monitoring including 3 or 5-lead ECG, non-invasive blood pressure, Masimo SET.
  • Motion tolerant SpO2, temperature, and drug calculations.
  • Offers various options to best meet your department’s needs including microstream, CO2, BISx Module, Nellcor, OxiMax, SpO2, cardiac output, continuous cardiac output/SvO2*, invasive blood pressures, ST and arrhythmia analysis and more.

Información adicional
MARCA

Datascope

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DISPLAY

  • Size: 12.1-inch (30.7cm) Color Active Matrix TFT LCD
  • Resolution: 800 x 600 pixels
  • Waveforms: 3 to 8

ECG (3-LEAD AND 5-LEAD)

  • Leads: I, II, III, aVR, aVL, aVF, V
  • Cable Detection: Autodetecting Datascope 3 or 5 wire
  • Display Sensitivity: 0.25, 0.5, 1.0, 2.0, 3.0, 4.0, cm/mV ± 10%
  • Frequency Response To Screen
  • Extended Mode: 0.05 – 100 Hz, -3db
  • Monitor Mode: 0.5 – 40 Hz, -3db
  • ST Mode: 0.05 – 40 Hz, -3db
  • ECG Sync Pulse for Cardioversion:
  • Delay: ≤35 ms max between QRS Peak and rising edge of Sync Pulse
  • Amplitude: 2Vp minimum into a 5k ohm load
  • Width: 2-7 ms
  • Analog Output: (ECG)
  • Delay: 25 ms max
  • Sensitivity: 1 V/mV of input, ± 10%
  • Defibrillator Overload Protection:
  • Withstand 360 Joule discharge as per IEC 60601-2-27, 51.101.1
  • Recovery Time: Time for recovery to within 1mV in < 8 seconds automatically. 3 seconds from 1Vpp at 60 Hz

HEART RATE METER

  • Range: 30 – 300 BPM Adult/Pediatric, 30 – 350 BPM
  • Neonate
  • Accuracy: ± 3 BPM or ± 3% at 30 – 250 BPM whichever is greater, ± 5% at 251 – 350 BPM
  • Pacer Rejection: Rejects all pulses of amplitude ± 2.0 mV to ± 700 mV and duration 0.1 to 2 ms with no tail. AAMI EC-13-1992 4.1.4
  • (3-Lead and 5-Lead) Rejects all pulses of amplitude ± 2.0 mV to 700 mV and duration 0.1 to 2ms with 100 ms time constant tail of less than 2.0 mV, or 4 ms time constant tail of < 2.0 mVper AAMI EC-13-1992 3.1.4.2 Tall T-Wave Rejection: Rejects all T-Waves of amplitude less than 120% of 1 mV, 100 ms QRS, T wave duration of 180 ms and Q-T interval of 350 ms per AAMI EC-13-1992 4.1.2.1 (c)

ST ANALYSIS

  • 3-lead or 5-lead Range: -9.9 mm to +9.9 mm
  • Resolution: 0.1 mm
  • Default ST Measuring Point: 80 ms after j point for HR <120 BPM, 60 ms after j point for HR >120 BPM

ARRHYTHMIA ANALYSIS

  1. 3-lead or 5-lead cables: Adult / Pediatric Only: Asystole, Irregular Heart Rate, Couplets, Bigeminy, Trigeminy, Ventricular Tachycardia, Ventricular Fibrillation, PVC’s per minute, Runs,
  2. Ventricular Rhythm

RESPIRATION (ECG)

  • Range: 4 to 199 BPM
  • Accuracy: ± 2% or 2 breaths per minute whichever is greater from 4 to 150 BPM, ± 4% from 151 to 199 BPM
  • Lead: I or II

NON-INVASIVE BLOOD PRESSURE

  • Technique: Oscillometric
  • Systolic Range: Adult: 55 – 235 mmHg, Pediatric: 55 – 160 mmHg, Neonate: 45 – 120 mmHg
  • Diastolic Range: Adult: 30 – 200 mmHg, Pediatric: 30 – 150 mmHg, Neonate: 20 – 100 mmHg
  • Systolic Accuracy: Mean Error less than ± 5 mmHg, standard deviation less than ± 8 mmHg
  • Diastolic Accuracy: Mean Error less than ± 5 mmHg, standard deviation less than ± 8 mmHg
  • Pulse Rate Range: Adult/Pediatric: 35 to 245 BPM Neonate: 70 to 245 BPM
  • Pulse Rate Accuracy: ±3 BPM or 3% whichever is greater
  • Connector Type: Rectus
  • Cuff Inflation: Volume of 500 cc to 300 mmHg in ≤35 sec

TEMPERATURE

  • Scale: Selectable C? or F?
  • Range: 15? to 45?C / 59? to 113?F (T1 and T2) 0?C to 5.5?C / 0?F to 9.9?F (Delta T)
  • Accuracy: ± 0.1?C (15?C to 45?C) exclusive of probe errors. ± 0.2?F (59?F to 113?F) exclusive of probe errors.

PULSE OXIMETRY

  • Masimo SET® SpO2 Accuracy Saturation with no motion conditions
  • Adult/Pediatric: 70% to 100% ± 2 digits SpO2, 0 to 69% unspecified
  • Neonate: 70% to 100% ± 3 digits SpO2, 0 to 69% unspecified
  • Ear Sensor (Adult/Pediatric): 70% to 100% ± 4 digits SpO2, 0 to 69% unspecified
  • Masimo SET® SpO2 Accuracy Saturation during motion conditions
  • Adult/Pediatric/Neonate: 70% to 100% ± 3 digits SpO2
  • Response Time: 18 seconds to 95% of final step of % SpO2 value from 60-95% at 75 BPM. Averaging set at 8 seconds.
  • Pulse Rate Range Masimo with no motion conditions
  • Adult/Pediatric/Neonate: 30-235 ±3 BPM, Ear Sensor (Adult/Pediatric) 30-235 ± 3 BPM
  • Pulse Rate Range Masimo during motion conditions Adult/Pediatric/Neonate: 30-235 ±5 BPM
  • Low Perfusion Performance
  • Masimo: > 0.02% Pulse Amplitude and % Transmission > 5% / Saturation (%SpO2) ± 2 digits; Pulse ± 3 digits
  • Nellcor® OxiMax® SpO2 Saturation Accuracy
  • Adult/Pediatric/Neonate: 70% to 100% ± 3 digits
  • Pulse Rate Range Nellcor: 20-249 ±3 BPM

IBP

  • Range: Sys/Dia/Mean -30 to +300 mmHg
  • Accuracy: ± 2 mmHg or 2% whichever is greater
  • Scale: -10 to 10, 0-20, 0-40, 0-160, 0-225, 0-320, 60-140 mmHg
  • Zero Range: ± 120 mmHg
  • Excitation: 5V DC ± 2%
  • Frequency Response: DC to 16 Hz ± 1Hz, -3db

RECORDER

  • Speed: 3.125, 6.25, 12.5, 25 mm, and 50 mm/sec
  • Note: 3.125 speed is for CO2/Resp only.

CO2 (MICROSTREAM®)

  • Range: 0 – 99 mmHg
  • Accuracy: 0 – 38 mmHg ± 4 mmHg 39 – 99 mmHg ± 12% (0 – 20 min)
  • 0 – 38 mmHg ± 2 mmHg 39 – 99 mmHg ± 5% + .08% for every 1mmHg above
  • 40 mmHg (> 20 min)
  • Respiration Rate: 0-150 breaths per minute
  • Respiration Accuracy: ± 1 breath per minute from 0 – 40 BPM
  • ± 2 BPM from 41– 70 BPM
  • ± 3% from 71 – 100 BPM
  • ± 5% from 101 – 150 BPM
  • CO2 Waveform Recognition: 5 mmHg ± 2 mmHg bandwidth
  • Start-up Time: 30 seconds typical
  • Sampling Rate: 50 ml/min ± 7.5 ml/min
  • Auto Zero: <15 seconds at 5, 10, 15 and 60 minutes, then every 60 minutes thereafter.

ELECTRICAL RATINGS

  • AC Voltage: 100 – 240 VAC ± 10%, 50/60 Hz ± 3 Hz
  • Battery Type: Sealed Lead Acid
  • Number of Batteries: 2
  • Battery Voltage: 12 V
  • Battery Capacity: 2.3 Ah
  • Battery Run Time: 1 hour, 20 min from two fully charged, new batteries at 25°C with ECG, SpO2 and NIBP running at 15 minute intervals
  • Recharge Time: 16 hrs max

PHYSICAL DIMENSIONS

  • Monitor Size: 26.7cm H x 30.2cm W x 18.8cm D 10.5″ H x 11.9″ W x 7.4″ D without module
  • 27.2cm H x 30.2cm W x 18.8cm D 10.7″ H x 11.9″ W x 7.5″ D with module
  • Weight: 5.43 kg (11.95 lbs) without optional accessories 7.04 kg (15.52 lbs) with 2 batteries, without optional accessories
  • 0.8 kg (1.75 lbs) module, without optional accessories

CARDIAC OUTPUT

  • Range: 0.2 to 20.0 liters/min
  • C.O. Repeatability: ± 2% or 0.02 l/min from the mean value
  • Blood Temp Range: 17.5°C to 43°C (63.5°F to 109.4°F)
  • Blood Temp Accuracy: ± 0.2°C (± 0.4°F) exclusive of probe errors
  • Injectate Temp Range: -1.0°C to 30.0°C (30.2°F to 86°F )
  • Injectate Temp Accuracy: ± 0.2°C (± 0.4°F) exclusive of probe errors

BIS (BISPECTRAL INDEX)

  • Bispectral Index (BIS) Range: 0 – 99
  • Signal Quality Index (SQI) Range: 0 – 100%
  • EMG Range: 30 – 80dB
  • Suppression Ratio (SR): 0 – 100%
  • Burst Count: 0 – 30
  • Input Impedance: >50 Mohm
  • Noise (RTI): <0.3uV RMS 0.25 – 50 Hz
  • Input Range: +/- 1mV
  • EEG Bandwidth: 0.25 – 100Hz (-3dB)
  • FILTERS (ON)
  • High Pass: 2.0 Hz (-3dB)
  • Low Pass: 70 Hz (-3dB)
  • Notch: 50 Hz and 60 Hz
  • FILTERS (OFF)
  • High Pass: 0.25 Hz (-3dB)
  • Low Pass: None
  • Notch: None

MAC (MINIMUM ALVEOLAR CONCENTRATION)

  • The Spectrum OR shall compute the uncorrected MAC value for all agents supported by the Gas Module SE using the following formula: Where AA is the anesthetic agent in use, ET AA is the end-tidal agent concentration, x(AA) is a clinically derived coefficient based on anesthetic
  • agent (known as 1MAC values), ET N2O is the end-tidal N2O concentration and x(N2O) is a clinically-derived coefficient for N2O (also known as the 1MAC value).
  • X(Isoflurane) = 1.15%
  • X(Halothane) = 0.77%
  • X(Sevoflurane) = 2.1%
  • X(Desflurane) = 7.3%
  • X(Enflurane) = 1.7%
  • X(N2O) = 105%
  • The uncorrected MAC value is not corrected for ambient pressure (altitude & barometric effects), patient age, patient core temperature or any other individual factors influencing the effect of volatile anesthetic agents. Reference Source: EN ISO 21647:2004 Medical electrical equipment-
  • Particular requirements for the basic safety and essential performance of respiratory gas monitors.
  • Vigilance® Interface: Supports the Vigilance IFM out communication protocol in accordance with Edwards Lifesciences specification ELS 1291 RevF