GE Healthcare Carescape V100 Vital Signs Monitor with SuperStat NIBP

GE Healthcare Carescape V100 Vital Signs Monitor with SuperStat NIBP Overview

On-the-go reliability.

In the general medical/surgical unit, you periodically check patients’ vital signs to monitor their status before and after treatment. A quick, reliable, easy-to-use vital signs monitor is essential in helping you care for many patients with efficiency.

The CARESCAPE™ V100 monitor can go with you from one patient to the next, enabling you to capture vital signs on your patients. It is specially designed to run cool so it does not need cooling fans. And since it has an IPX1 water and dust penetration rating, it supports infection control and cleaning. With speed, accuracy and connectivity, the CARESCAPE V100 monitor helps you manage Clinical Information Logistics™ by collecting the right information at the point of care, and presenting it wherever it is needed. So you can make fast, quality care decisions informed by relevant, current clinical intelligence.

Clinical excellence inside.

By combining fast determination times with an advanced algorithm, the CARESCAPE V100 monitor helps ensure patient comfort while maintaining a high standard of clinical accuracy. It also includes the same advanced parameters and algorithms as other higher acuity GE monitors, ensuring measurement consistency across all care areas.

• GE DINAMAP® SuperSTAT™, Classic or ausculatory blood pressure algorithms support speed, comfort and artifact rejection.
• Choose from three Sp02 measurements including GE Ohmeda®, Nellcor® or Masimo®.
• Alaris® Turbo Temp® thermometry, featuring oral temperature determinations in about 7 seconds.

Mobility and connectivity.

The durable CARESCAPE V100 vital signs monitor is designed for sub-acute clinical settings where monitor mobility is important. Not only can it withstand the rigors of tough clinical use and cleaning, the CARESCAPE V100 monitor battery has a long run time – typically eight hours before requiring recharge. This extended battery life allows the flexibility to move the monitor from one patient room to the next for an entire shift. In addition, the CARESCAPE V100 monitor can be connected to the GE CARESCAPE Network. That means vital signs data is accessible on the CARESCAPE CIC Pro®, CARESCAPE iPanel™, CARESCAPE Mobile Viewers™ or anywhere it is needed for making fast, efficient care decisions.

Vital signs data captured by the CARESCAPE V100 monitor can also be integrated with the GE Centricity® EMR and Siemens® EMR.

The CARESCAPE V100 delivers the speed, accuracy and mobility you require when capturing patient vital signs. It also offers a new level of connectivity that helps you improve Clinical Information Logistics across your organization. By integrating vital patient data into a seamless record of clinical intelligence, the CARESCAPE V100 enables you to access the right information at the right time and place – helping you care for many patients with efficiency.

The quality you expect.

The CARESCAPE V100 is designed for care areas where patients require vital signs measurements. The CARESCAPE V100 is the ideal "2 in 1" device. Its ease of mobility and versatility mean that it can either be used for continuous monitoring or for routine checks of vital signs, without needing to take up valuable nursing time. In this way, it considerably increases overall productivity. The monitor's ruggedness, with the eight hour battery life,1 gives you the reliability and mobility you need to monitor patients throughout the unit. With non-invasive blood pressure determination times as fast as 14 seconds and the clinical accuracy of embedded GE DINAMAP technology, the CARESCAPE V100 monitor delivers the speed and accuracy you expect. Common tasks require only one step, making it fast and easy to use. Plus, connectivity to the GE Centricity EMR or Siemens EMR creates a seamless patient record regardless of where care is being delivered.

GE Healthcare Carescape V100 Vital Signs Monitor Specifications

Mechanical Dimensions
Height: 7.7 in (19.5 cm)
Width:
8.6 in (21.9 cm) without temperature
10.0 in (25.4 cm) with temperature
Depth: 5.3 in (13.5 cm)
Weight: 5.4 lb (2.4 kg) including battery
Mountings: Self-supporting on rubber feet or pole mounted
Portability: Carried by recessed handle

Power Requirements
Power converter universal P/N: 2018859-001
Protection against electrical shock: Class II
AC input: Voltage 100 to 250VAC, 12VA
DC output: Voltage 12VDC at 1A

The AC mains power adapter contains a nonresettable and nonreplaceable fuse.

Monitor
Protection against electrical shock: Internally powered or Class II when powered from specified external power supply.
DC input voltage: 12 VDC, supplied from a source conforming to IEC 60601-1.
Battery: Refer to “Battery” Section

Fuses: The monitor contains three fuses. The fuses are mounted within the monitor. The fuses protect the low voltage DC input, the battery, and the remote alarm output. The +5 V output on the host port connector is regulated by internal supply.

Environmental
Operating Temperature: + 5°C to + 40°C (+ 41°F to + 104°F)
Operating Atmospheric Pressure: 700 hPa to 1060 hPa

Storage/Transportation Storage Temperature:
– 20°C to + 50°C
(– 4°F to + 122°F)
Atmospheric Pressure: 500 hPa to 1060 hPa
Humidity Range: 5% to 95% noncondensing

Radio Frequency: Complies with IEC Publication 60601-1-2 (2001). Medical Electrical Equipment, Electromagnetic Compatibility Requirements and Tests and CISPR 11 (Group 1, Class B) for radiated and conducted emissions

Alaris Turbo-Temp Specs

Scale: °Fahrenheit (F); °Celsius (C)

Range
Predictive mode:
Max: 41.1°C; 106.0°F
Min: 35.6°C; 96.0°F

Monitor mode:
Max: 41.1°C; 106.0°F
Min: 26.7°C; 80.0°F

Monitor mode accuracy: ±0.1°C; ±0.2°F
(when tested in a calibrated liquid bath; meets ASTM E1112, Table 1, in range specified)

Determination time approximately 7 seconds, typical

NOTE: Use only IVAC probes and P850A probe covers. The size, shape, and thermal characteristics of the probe covers can affect the performance of the instrument. Inaccurate readings or retention problems may occur unless IVAC® probes and probe covers are used.

Printer Spec
Printer type: Thermal dot array
Resolution: 384 dots/inch horizontal
Paper type: The paper roll used by the printer must be compatible with GE PN 770137.
Languages printed: English, German, French, Italian, Spanish, Portuguese (Brazil and Portugal), Hungarian, Polish, Czech, Finnish, Swedish, Danish, Dutch, Norwegian, and Slovak

Battery Specs
Capacity:
6V; 3.3 Ahr sealed lead acid battery protected by internal auto-resetting fuse and thermal protection

Battery Life:
8.1 hours with a usage scenario of: NIBP determinations every 15 minutes with SpO2 and temperature active.
11.5 hours non-SpO2 versions with a usage scenario of: NIBP determinations every 15 minutes with temperature active.

Charge time:
Approximately 5 hours from full discharge when the monitor is off. Approximately 8 hours when the monitor on.

Nellcor Oxi-Max Specifications

Measurement Range
SpO2: 1 to 100%
Pulse Rate: 20 to 250 bpm
Perfusion Range: 0.03 to 20%

Accuracy
Saturation
Adult*: 70 to 100% ±2 digits
Neonate*: 70 to 100% ±3 digits
Low Perfusion**: 70 to 100% ±2 digits

Pulse Rate
Adult and neonate: 40 to 250 bpm ±3 digits
Low Perfusion**: 40 to 250 bpm ±3 digits

*Adult specifications are shown for OxiMax® MAX-A and MAX-N sensors with the N-600. Saturation accuracy will vary by sensor type. This variation equals plus or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.

**Applicability: OxiMax MAX-A, MAX-AL, MAX-P, MAX-I, and MAX-N sensors.

Oxi-Max Sensor Accuracy
NOTE: All Nellcor® OxiMax sensors must be used with the Nellcor cable; the DOC-10 cable. RS-10 and Oxisensor® II sensors are not compatible with the V100 Vital Signs Monitor. Sensor Model SpO2 Range 70% to 100%

OxiMax
MAX-A, MAX-AL: ±2 digits
MAX-N* (adult): ±2 digits
MAX-N** (neonate): ±3 digits
MAX-P: ±2 digits
MAX-I: ±2 digits
MAX-FAST: ±2 digits
SC-A (adult): ±2 digits
SC-PR (neonate): ±3 digits
SC-NEO: ±3 digits
MAX-R†: ±3.5 digits

OxiCliq®
OxiCliq A: ±2.5 digits
OxiCliq P: ±2.5 digits
OxiCliq N*: (adult) ±2.5 digits
OxiCliq N**: (neonate) ±3.5 digits
OxiCliq I: ±2.5 digits

Reusable Sensor Models
D-YS* (infant to adult): ±3 digits
D-YS** (neonate): ±4 digits
D-YS & D-YSE: ±3.5 digits
D-YS & D-YSPD: ±3.5 digits
DS-100A: ±3 digits
OXI-A/N*: (adult) ±3 digits
OXI-A/N**: (neonate) ±4 digits
OXI-P/I: ±3 digits

Sensor Light Source
Wavelength‡
Infrared: 890 nm (nominal)
Red: 660 nm (nominal)

Power Dissipation
Infrared: 22.5mW (max)
Red: 30 mW (max)

* The MAX-N, D-YS, OXI-A/N, and OxiCliq N were tested on patients >40 kg.

** Neonatal Sensor Accuracy: When sensors are used on neonatal subjects as recommended, the specified accuracy range is increased by ±1 digit, as compared to adult usage, to account for the theoretical effect on oximeter measurements of fetal hemoglobin in neonatal blood. For example, MAX-N accuracy on neonates is ±3 digits, rather than ±2 digits.

† The accuracy specification has been determined between saturations of 80%-100%.

‡ Information about wavelength range can be especially useful to clinicians.

Factory Default Settings
SpO2 HIGH Alarm Limit: 100%
SpO2 LOW Alarm Limit: 90%
Response mode (for Mode 1: Normal Response): 1
SatSeconds™: 0

Masimo SET Specifications

Measurement Range
SpO2: 1 to 100%
Pulse Rate: 25 to 240 bpm
Perfusion Range: 0.02 to 20%

Accuracy and Motion Tolerance
Saturation
Without Motion adult/pediatric*: 70 to 100% ±2 digits
Without Motion neonate*: 70 to 100% ±3 digits
With Motion adult/ped/neonate**†: 70 to 100% ±3 digits
Low Perfusion‡:
70 to 100% ±2 digits
0 to 69% unspecified

Pulse Rate
Without Motion: 25 to 240 bpm ±3 digits
With Motion:
normal physiologic range
25 to 240 bpm ±5 digits

* The Masimo SET® SpO2 parameter with LNOP-Adt sensors has been validated for no motion accuracy in human blood studies on healthy adult volunteers in induced hypoxia studies in the range of 70-100% SpO2 against a laboratory CO-oximeter and ECG monitor. This variation equals plus or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.

** The Masimo SET SpO2 parameter eith LNOP-Adt sensors has been validated for motion accuracy in human blood studies on healthy adult volunteers in induced hypoxia studies while performing rubbing and tapping motions at 2 to 4 Hz at an amplitude of 1 to 2 cm and a nonrepetitive motion between 1 to 5 HZ at an amplitude of 2 to 3 cm in induced hypoxia studies in the range of 70-100% SpO2 against a laboratory CO-oximeter and ECG monitor. This variation equals plus or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.

† The Masimo SET SpO2 parameter with LNOP-Neo Pt sensors has been validated for neonatal motion accuracy in human blood studies on neonates while moving the neonate‘s foot at 2 to 4 cm against a laboratory CO-oximeter and ECG monitor. This variation equals plus or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.

‡ The Masimo SET SpO2 parameter has been validated for low perfusion accuracy in bench top testing against a Biotek index 2 stimulator and Masimo‘s simulator with signal strengths of greater than 0.02% and a % transmission of greater than 5% for saturations ranging from 70 to 100%. This variation equals plus or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.

Low Perfusion Performance
0.02% Pulse amplitude:
Saturation (% SpO2)
± 2 digits
% transmission >5%: Pulse rate ± 3 digits

Interfering substances: Carboxyhemoglobin may erroneously increase readings. The level of increase is approximately equal to the amount of carboxyhemoglobin present. Dyes, or any substance containing dyes, that change usual arterial pigmentation may cause erroneous readings.

Masimo Sensor Accuracy
Sensor Model: Sensor model SpO2 range 70% to 100%

LNOP
LNOP ADT: ± 2 digits without motion
LNOP NEO: ± 3 digits without motion
LNOP NEO-L:
Foot ± 3 digits without motion
Finger ± 2 digits without motion
LNOP NEO PT-L: ± 3 digits without motion
LNOP Adtx: ± 2 digits without motion
LNOP Pdtx: ± 2 digits without motion
LNOP DCI: ± 2 digits without motion
LNOP DCIP: ± 2 digits without motion
LNOP Hi Fi-Neo/adult:
Foot ± 3 digits without motion
Finger ± 2 digits without motion
LNOP Hi Fi-Infant/Ped: ± 2 digits
LNOP Blue Infant Thumb/Toe*:
± 3 digits (for 80-100) without motion
± 4 digits (for 60-80) without motion
± 3.3 digits (for 70-100) without motion
LNOP YI: Multi-Site
Foot/hand ± 3 digits without motion
Finger/toe ± 2 digits without motion
LNOP DC-195: ± 2 digits without motion
LNOP TC-I: ± 3.5 digits without motion

LNCS
LNCS TCI: ± 3.5 digits without motion
LNCS DC-I: ± 2 digits without motion
LNCS DC-IP: ± 2 digits without motion
LNCS Adult Adtx: ± 2 digits without motion
LNCS Ped Pdtx: ± 2 digits without motion
LNCS Infant-L: ± 2 digits without motion
LNCS Neo PT-L: ± 3 digits without motion

Resolution
Saturation (% SpO2): 1%
Pulse rate(bpm): 1

Sensor Light Source
Wavelength**
Infrared: 905 nm (nominal)
Red: 660 nm (nominal)

Power Dissipation
Infrared: 27.5 mW (max)
Red: 30 mW (max)

* Masimo SET Technology with LNOP Blue sensors have been validated for no motion accuracy in human blood studies on neonatal, infant and pediatric patients with congenital, cyanotic cardiac lesions in the range of 60% to 100% SpO2 against a laboratory CO-oximeter. This variation equals plus or minus one standard deviation, which encompasses 68% of the population.

** Information about wavelength range can be especially useful to clinicians.

NIBP Specifications

Cuff Pressure Range (Normal operating range):
0 to 290 mmHg (adult/ped)
0 to 145 mmHg (neonate)
Blood Pressure Accuracy: (SuperSTATTM NIBP algorithm)
Blood Pressure Accuracy: (Classic and Auscultatory)
Meets ANSI/AAMI Standard: SP-10:1992 (mean error ≤5 mmHg, standard deviation ≤8 mmHg)
Meets ANSI/AAMI Standard: SP-10:2002 (mean error ≤5 mmHg, standard deviation ≤8 mmHg)
Maximum Determination:
120 s (adult/ped)
85 s (neonate)
Overpressure Cutoff: 300 to 330 mmHg (adult/ped) 150 to 165 mmHg (neonate)

Systolic:
30 to 290 mmHg (adult/ped)
30 to 140 mmHg (neonate)

MAP:
20 to 260 mmHg (adult/ped)
20 to 125 mmHg (neonate)

Diastolic:
10 to 220 mmHg (adult/ped)
10 to 110 mmHg (neonate)

Systolic:
30 to 245 mmHg (adult/ped)
40 to 140 mmHg (neonate)

MAP:
15 to 215 mmHg (adult/ped)
30 to 115 mmHg (neonate)

Distolic:
10 to 195 mmHg (adult/ped)
20 to 100 mmHg (neonate)

Pulse Rate Range (SuperSTAT NIBP algorithm):
30 to 240 beats/min (adult/ped)
30 to 240 beats/min (neonate)

Pulse Rate Range (Classic and Auscultatory):
30 to 200 beats/min (adult/ped)
30 to 220 beats/min (neonate)

Pulse Rate Accuracy: ± 3.5% or 3 bpm

NOTE: All CARESCAPE V100 monitor regulatory and accuracy studies have been performed using CRITIKON® Blood Pressure cuffs. The size, shape, and bladder characteristics can affect the performance of the monitor.

GE Ohmeda® SpO2 Specifications

Measurement Range
SpO2: 1 to 100%
Pulse Rate: 30 to 250 bpm
Perfusion Range: 0.03 to 20%

Accuracy
Saturation

Adult:
70 to 100% ±2 digits whichever is greater, (without motion)

Neonate*:
70 to 100% ±3 digits (without motion)

Adult/Neonate**:
70 to 100% ±3 digits (during clinical motion)

Low Perfusion:
70 to 100% ±2 digits (during clinical low perfusion)

Pulse Rate
Adult/Neonate:
30 to 250 bpm: ± 2 digits or ± 2%, whichever is greater, (without motion)
30 to 250 bpm: ± 5 digits (during motion)

Low Perfusion: 30 to 250 bpm ±3 digits

*SpO2 measurement accuracy is based on deep hypoxia studies using OxyTip+® sensors on healthy adult volunteer subjects. Arterial blood samples were analyzed simultaneously on multiple CO-oximeters. This variation equals plus or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.

**Applicability: OXY-AF and OXY-AP sensors. NOTE: Accuracy may vary for some sensors; always check the instructions for the sensor.

GE Ohmeda Sensor Accuracy
Sensor Model: SpO2 Range 70% to 100%

OxiTip+
OXY-F-UN: ±2 digits without motion
OXY-W-UN: ±2 digits without motion
OXY-E-UN: ±2 digits without motion
OXY-SE: ±2 digits without motion
OXY-AP: ±2 digits without motion
OXY-AF: ±2 digits without motion
OXY-F2-GE: ±2 digits without motion
OXY-F4-GE: ±2 digits without motion
OXY-E2-GE: ±2 digits without motion
OXY-E4-GE: ±2 digits without motion

Sensor light source
Wavelength*
Infrared: 930 to 950 nm (nominal)
Red 650 to 670 nm (nominal)

Average power: < 1 mW

* Information about wavelength range can be especially useful to clinicians.