Nothing Special   »   [go: up one dir, main page]

Brosur Spesifikasi Produk

Download as pdf or txt
Download as pdf or txt
You are on page 1of 7

CARESCAPE V100

Vital signs monitor


Connecting intelligence and care.

The CARESCAPE* V100 monitor is designed for care areas


where patients require vital signs measurements. It can go
with you from one patient to the next, and because of its
speed, accuracy and connectivity, the CARESCAPE V100
monitor collects the right information at the point of care to
help you make fast, quality care decisions.

Features
Can be used for spot-checking or for continuous monitoring,
providing you the flexibility of a 2 in 1 device
Designed for adult and pediatric use, as well as neonatal
patients with very low perfusion rates
Includes the same advanced parameters and algorithms as
other higher acuity GE monitors, helping ensure measurement consistency across all care areas
Non-invasive blood pressure measurement uses GEs
exceptional DINAMAP* technology
Three choices for pulse oximetry include GE TruSignal,*
Nellcor OxiMax or Masimo SET
Three options for temperature include Exergen
TemporalScanner, Alaris Turbo Temp and Alaris Tri-Site
Allows for inflation setpoints, so you can be sensitive to
patients special circumstances and ensure their comfort
Large display makes it easy to read even from a distance
Stores up to 40 measurements for up to 24 hours with the
capability to print strips
Designed for easy serviceability and simple fieldreplacement kits

Connectivity can be made with a PC or other third-party


connectivity solutions such as Capsule Technologie
and Cerner
Typical battery life of up to 11 hours before requiring
recharge. If the battery is discharged, it maintains the data
Connect up to three additional accessories simultaneously
with the DINAMAP Serial Hub, via the monitors HostComm
(sold separately)

Technical specifications

GE sensor accuracy
Sensor model

SpO2 range 70 to 100%

Portability Carried by recessed handle or on


a roll stand

TruSignal

Printer

TS-F-D3

2 digits without motion

Printer type

Thermal dot array

TS-W-D

2 digits without motion

Resolution

384 dots/inch horizontal

TS-E-D3

3 digits without motion

Paper type

Must be compatible with

TS-SE-33

2 digits without motion

GE PN 770137

TS-AF-103

2 digits without motion

TS-AF-25

2 digits without motion

TS-F2-GE

2 digits without motion

TS-F4-GE

2 digits without motion

TS-E2-GE

3 digits without motion

TS-E4-GE

3 digits without motion

Languages printed English, German, French, Italian,


Spanish, Portuguese, Hungarian,
Polish, Czech, Finnish, Swedish,
Danish, Dutch, Norwegian,
and Slovak

Temperature options
Exergen TemporalScanner temporal artery thermometer
Alaris Turbo Temp thermometer
Alaris Tri-site thermometer

NIBP options
GE DINAMAP SuperSTAT*
GE DINAMAP Classic (intra-arterial or auscultatory reference)

Performance specifications
GE TruSignal SpO2 specifications
Measurement range
SpO2

1 to 100%

Pulse rate

30 to 250 bpm

TS-SA4-GE
TS-SA-D3
For TS-SA4-GE and TS-SA-D sensors the accuracy
range is as following
70 to 100% 90 to 100% 80 to 90% 70 to 80% below 70%
2 digits
1 digits
2 digits 3 digits unspecified
Sensor light source
Wavelength4 Infrared: 930 to 950 (nominal)
Red: 650 to 670 (nominal)
Maximum output
power for each LED

< 15mV

Accuracy
Saturation
Adult 70 to 100% 2 digits
(without motion)
Neonate1 70 to 100% 3 digits
(without motion)
Adult/Neonate2 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

Note: Accuracy may vary for some sensors; always check the
instructions for the sensor.

(1) SpO2 measurement accuracy is based on deep hypoxia studies using TruSignal
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.
(2) Applicability: TS-AF sensors.
(3) Requires compatible interconnect cable TS-G3
(4) Information about wavelength range can be especially useful to clinicians.

Performance specifications (continued)


Masimo SET specifications5
Measurement range
SpO2

1 to 100%

Pulse rate

25 to 240 bpm

Perfusion range

0.02 to 20%

Accuracy and motion tolerance


Saturation

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 accuracy10

Without motion
adult/pediatric6

70 to 100% 2 digits

Without
motion neonate6

70 to 100% 3 digits

With motion
adult/ped/neonate7, 8

70 to 100% 3 digits

Low perfusion 70 to 100% 2 digits


0 to 69% unspecified
9

Pulse rate
Without motion

Low perfusion performance

25 to 240 bpm 3 digits

With motion Normal physiologic range


25 to 240 bpm 5 digits

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

(5) Masimo CSD-1201 (MS-2011 specifications cleared by the FDA).

2 digits

LNOP Blue Infant Thumb/Toe11


3 digits (for 80-100) without motion
4 digits (for 60-80) without motion
3.3 digits (for 70-100)
without motion

(6) 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.

LNOP YI Multi-Site Foot/hand 3 digits without motion


Finger/toe 2 digits without motion
LNOP DC-195

2 digits without motion

(7) The Masimo SET SpO2 parameter with 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.

LNOP TC-I

3.5 digits without motion

(8) 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
neonates 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.
(9) The Masimo SET SpO2 parameter has been validated for low-perfusion accuracy in
bench-top testing against a Bio-Tek Index 2 simulator and Masimos 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.
(10) Masimo CSD-1109 (sensor specification)
(11) 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.

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

Performance specifications (continued)

Sensor model

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

OxiMax sensor accuracy16

Sensor light source


Wavelength12 Infrared: 905 nm (nominal)
Red: 660 nm (nominal)

SpO2 range 70 to 100%

Note: A
 ll Nellcor OxiMax sensors must be used with the Nellcor
cable; the SCP-10 cable. RS-10 and Oxisensor II sensors are
not compatible with the CARESCAPE V100 monitor.

OxiMax
MAX-A, MAX-AL

2 digits

MAX-N (adult)

2 digits

MAX-N (neonate)

3 digits

Nellcor OxiMax specifications13

MAX-P

2 digits

Measurement range

MAX-I

2 digits

Power dissipation Infrared: 22.5 mW (max)


Red: 27.5 mW (max)

17

SpO2

1 to 100%

MAX-FAST

2 digits

Pulse rate

20 to 250 bpm

SC-A (adult)

2 digits

Perfusion range

0.03 to 20%

SC-PR (neonate)

3 digits

Accuracy

SC-NEO

3 digits

Saturation

MAX-R18

3.5 digits

Adult14

70 to 100% 2 digits

OxiCliq

Neonate14

70 to 100% 3 digits

OxiCliq A

2.5 digits

Low perfusion15

70 to 100% 2 digits

OxiCliq P

2.5 digits

Pulse rate

OxiCliq N (adult)

2.5 digits

Adult and neonate

20 to 250 bpm 3 digits

OxiCliq N (neonate)

3.5 digits

Low perfusion15

20 to 250 bpm 3 digits

OxiCliq I

2.5 digits

17

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


Wavelength19 Infrared: 890 nm (nominal)
Red: 660 nm (nominal)
(12) Information about wavelength range can be especially useful to clinicians.
(13) Nellcor N600x Operators Manual
(14) 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. Accuracy is based on deep hypoxia studies on healthy
adult volunteer subjects. Arterial blood samples were analyzed simultaneously on
multiple CO-oximeters.
(15) Applicability: OxiMax MAX-A, MAX-AL, MAX-P, MAX-I, and MAX-N sensors.
(16) Nellcor oxygen saturation accuracy specification grid (DOC0318495)
(17) The MAX-N, D-YS, OXI-A/N, and OxiCliq N were tested on patients >40 kg.
(18) The accuracy specification has been determined between saturations of
80% to 100%.
(19) Information about wavelength range can be especially useful to clinicians.

Power dissipation Infrared: 22.5mW (max)


Red: 30 mW (max)
Note: 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.

Performance specifications (continued)


NIBP specifications
Cuff pressure range

0 to 290 mmHg (adult/ped)

0 to 145 mmHg (neonate)


(Normal operating range)
Blood pressure accuracy
DINAMAP SuperSTAT
NIBP algorithm

Mean error 5 mmHg,

NIBP algorithm Standard deviation 8 mmHg


(Meets ANSI/AAMI Standard
SP10:1992)
Classic and auscultatory Mean error 5 mmHg,
standard deviation 8 mmHg
(Meets ANSI/AAMI Standard
SP10:2002)
Maximum
determination time

120 s (adult/ped)
85 s (neonate)

Exergen TemporalScanner specifications


Accuracy

0.1C or 0.2F

Temperature range

61 to 110F (16 to 43C)

Operating environment 60 to 104F (16 to 40C) (ambient)


Arterial heat
balance range for
body temperature20

94 to 110F (34.5 to 43C)

Resolution

0.1F or 0.1 C

Response time

0.04 seconds (approx.)

Alaris Turbo Temp specifications


Accuracy21

0.2F or 0.1C

Temperature range
Predictive mode

96 to 106F (35.6 to 41.1C)

Monitor mode

80 to 107.9F (26.7 to 42.1C)

Response time

As fast as 7 seconds

Alaris Tri-Site specifications


0.2F or 0.1C

Overpressure cutoff 300 to 330 mmHg (adult/ped)


150 to 165 mmHg (neonate)

Accuracy21

Blood pressure range

Predictive mode

95 to 106F (35 to 41.1C)

DINAMAP SuperSTAT
NIBP algorithm

Monitor mode

80 to 107.9F (26.7 to 42.1C)

Response time

As fast as 11 seconds

Systolic 30 to 290 mmHg (adult/ped)


30 to 140 mmHg (neonate)
MAP 20 to 260 mmHg (adult/ped)
20 to 125 mmHg (neonate)

Temperature range

Note: To ensure accurate measurements, use only recommended


blood pressure cuffs available from GE.

Diastolic 10 to 220 mmHg (adult/ped)


10 to 110 mmHg (neonate)
Classic and auscultatory
Systolic 30 to 245 mmHg (adult/ped)
40 to 140 mmHg (neonate)
MAP 15 to 215 mmHg (adult/ped)
30 to 115 mmHg (neonate)
Diastolic 10 to 195 mmHg (adult/ped)
20 to 100 mmHg (neonate)
Pulse rate range
SuperSTAT

30 to 240 beats/min (adult/ped)

NIBP algorithm

30 to 240 beats/min (neonate)

Classic and auscultatory 30 to 200 beats/min (adult/ped)


30 to 220 beats/min (neonate)
Pulse rate accuracy 3.5% or 3 bpm, whichever
is greater
Note: To ensure accurate measurements, use only recommended
blood pressure cuffs available from GE.

(20) Automatically applied when temperature is within normal body


temperature range, otherwise reads surface temperature.
(21) When tested in a calibrated liquid bath; meets ASTM E1112, Table 1,
in range specified. Accuracy measured in continuous (monitor) mode.

Power specifications

Physical specifications

AC input voltage

100 to 250VAC, 12VA

DC output voltage

12VDC at 1A

Dimensions (H x W x D) 19.5 x 21.9 x 13.5 cm


(7.7 x 8.6 x 5.3 in)

The AC mains power adapter


contains a non-resettable and
non-replaceable fuse

19.5 x 25.4 x 13.5 cm


(7.7 x 10 x 5.3 in) with Alaris
temperature option

Protection against
electrical shock Internally powered or Class II when
powered from specified external
power supply

Weight

DC input voltage 12 VDC, supplied from a source


conforming to IEC 60601-1

Height to
mounting platform 101 cm (40 in) from floor to
lowest position
144 cm (45 in) from floor to
highest position

Fuses Monitor contains three fuses,


mounted within. 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

Battery
Type

Sealed lead acid, 6V, 3.3 Ahr

Battery life 5 hours with NIBP every 5 minutes


and SpO2, temperature and printer
active 11.5 hours non-SpO2 versions
with a usage scenario of: NIBP
determinations every 15 minutes
without temperature active
Charge time Approximately 5 hours from full
discharge when the monitor is off.
Approximately 8 hours when the
monitor is on

Environmental specifications
Operating conditions
Temperature

41 to 104F (5 to 40C)

Atmospheric pressure

500 hPa to 1060 hPa

2.4 kg (5.4 lbs) including battery

Mountings Self-supporting on rubber feet, pole


mounted,22 or wall mount bracket

DINAMAP Mobility Workstation roll stand (optional)

Base Diameter 53.3 cm (21 in)


5-7.1 cm (2.8 in) casters 3 locking
Accessories (H x W x D)
Accessory bin 10.2 x 33.3 x 22.4 cm
(4.0 x 13.1 x 8.8 in)
Surface tray 3.0 x 30.0 x 5.5 cm
(1.2 x 11.8 x 2.2 in)
Rear canister bin 10.7 x 13.5 x 13.0 cm
(4.2 x 5.3 x 5.1 in)
Weight

8.0 kg (17.5 lbs)

Warranty
Two year standard warranty.

Certifications
UL 60601-1, CAN/CSA C22.2 No. 601.1, IEC 60601-1,
IEC 60601-1-2, IEC 60601-1-4, IEC 60601-1-8,
IEC 60601-2-30, IEC 60601-2-49, EN 1060-1, EN 1060-3,
ISO 9919 CE marked to the Medical Devices Directive - 93/42/
EEC

Storage conditions
Storage temperature

-4 to 122F (-20 to 50C)

Humidity range

5% to 95% noncondensing

Radio frequency Complies with IEC 60601-1-2.


Medical Electrical Equipment,
Electromagnetic Compatibility
Requirements and Tests and CISPR
11 (Class B, Group 1) for radiated
and conducted emissions

(22) Pole mount option not available on the DINAMAP Mobility Workstation roll stand.

About GE Healthcare
GE Healthcare provides transformational medical technologies and
services to meet the demand for increased access, enhanced quality and
more affordable healthcare around the world. GE (NYSE: GE) works on
things that matter great people and technologies taking on tough
challenges. From medical imaging, software & IT, patient monitoring
and diagnostics to drug discovery, biopharmaceutical manufacturing
technologies and performance improvement solutions, GE Healthcare
helps medical professionals deliver great healthcare to their patients.
GE Healthcare
8200 West Tower Avenue
Milwaukee, WI 53223
U.S.A.

GE Healthcare Asia Pacific


Japan
4-7-127, Asahigaoka
Hino-shi, Tokyo
191-8503 Japan
Tel: +81 42 585 5111

ASEAN
1 Maritime Square #13-01
HarbourFront Centre
Singapore 099253
Tel: +65 6291 8528

ANZ
Building 4B, 21 South St
Rydalmere NSW 2116
Australia
Tel: 1300 722 229

Korea
8F, POBA Gangnam Tower
343, Hakdong-ro, Gangnam-gu
Seoul 135-820, Korea
Tel: +82 2 6201 3114

8 Tangihua Street
Auckland 1010
New Zealand
Tel: 0800 434 325

2013 General Electric Company All rights reserved.


GE and GE Monogram are trademarks of General Electric Company.
GE Healthcare, a division of General Electric Company.
GE Healthcare Finland Oy, a General Electric company, doing business as GE Healthcare.
* Trademark of General Electric Company.
Capsule is a trademark of Capsule Technologie (Capsule Tech, Inc.).
Cerner is a registered trademark of Cerner Innovation, Inc.

www.gehealthcare.com

Exergen and TemporalScanner are trademarks of Exergen Corporation.


Alaris and Turbo Temp are registered trademarks of Alaris Medical Systems, Inc.
OxiCliq, OxiMAX, Oxisensor, SatSeconds and Nellcor are trademarks of Nellcor Puritan
Bennett, Inc.
Masimo SET is a trademark of Masimo Corporation.

GE imagination at work

GE Healthcare reserves the right to make changes in specifications and features shown
herein, or discontinue the product described at any time without notice or obligation.
Contact your GE Healthcare representative for the most current information.
DOC0385787 rev5 6/13-EN-Asia Pacific Printed in China July 2013

You might also like