X40+ Oxi-Capnography

X40+ Oxi-Capnography Monitor

Omya’s Hand-Held Capnograph & Pulse Oximeter with Masimo Technology is an exceptionally comprehensive and versatile device intended for both spot checks and continuous monitoring. This hand-held portable monitor facilitates simultaneous end-tidal CO2 and SpO2 measurements is a variety of medical settings, including EMS/ED, transport, critical care, operating room, sleep lab and for procedural sedation.

Applications and Benefits

For EMS Transport

Capnography is a valuable tool during emergency transport of both intubated and non-intubated patients for proper assessment of the patient’s ventilatory status.

For Conscious Sedation

When performing procedural sedation, ensuring patient safety and adequate ventilation is essential.

For Cardiopulmonary Resuscitation

Capnography is a valuable tool during cardiopulmonary resuscitation (CPR) of intubated patients.

For Pain Management

The use of capnography is becoming more widespread for patients receiving opiates for acute pain management.

For Sleep Laboratories

When conducting sleep studies, it is important to accurately and consistently measure exhaled CO2 levels in order to reliably assess the quality of ventilation during sleep.

A care solution designed specifically for the Neonatal patient and their environment

Specialised wide-range of neonatal algorithms for accurate, easy, and informed decision making, Completely valid and customizable alarms limits for ICU use.

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Acuity Areas

– Emergency Medical Services (EMS) in the field or during transport
– Outpatient or Ambulatory Surgery centers; special procedures area
– General medical/surgical hospital ward
– ICU, Emergency Department
– Hospital-based or free-standing sleep laboratory
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Clinical Application

– Airway management for all intubated patients
– Procedural or conscious sedation-adequacy of ventilation.
– Patient safety during patient-controlled analgesia (PCA) or continuous narcotic administration.
– Sleep studies
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Acuity Areas

– Emergency Medical Services (EMS) in the field or during transport
– Outpatient or Ambulatory Surgery centers; special procedures area
– General medical/surgical hospital ward
– ICU, Emergency Department
– Hospital-based or free-standing sleep laboratory
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Clinical Application

– Airway management for all intubated patients
– Procedural or conscious sedation-adequacy of ventilation.
– Patient safety during patient-controlled analgesia (PCA) or continuous narcotic administration.
– Sleep studies
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Interfaces

12″ large color LCD display with 170° vertical and
horizontal viewing angle and up to eight waveforms
provides you with better visibility of complete patient data.
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Oxygen Cardiorespirogram (Oxy CRG)

The oxygen-cardiorespirography helps the
physician measure beat-to-beat heart rate,
respiratory rate and thoracic impedance
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Apnea judgement time adjustment

By monitoring Apnea, the user can detect the
cessation of breathing easily.
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Dual SpO2 detection

Dual SpO2 helps to detect persistent pulmonary hypertension of the newborn  of the newborn which causes inequalities of the SpO2-measurement between the right upper and left lower limbs.
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Arrhythmia analysis

Arrhythmia analysis provides the superior elimination of false alarms and reducing events of alarm fatigue.
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Lithium-ion battery

Lithium-ion battery for longer operation, short
recharging time and a low-toxicity battery solution
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State of the Art Technology

Dual Micro-controller, Driven by Precise Stepper Motor, Concealed
Mechanism, Quiet Operation Communication Interfaces
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Ergonomic Design

3 inch Wide LCD display, Recessed Handle,
Numeric Keypad for Fast Input and Quick Access Setting
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Patient Care in one touch

Dual Visual Alarms, Automatic keypad Lock Activation,
Dynamic Occlusion Detection, Anti-Bolus Functions
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Intuitive Touchscreen

Combining a simple, single level menu structure with all important trends and parameters without hiding current waveforms makes an intuitive touch screen makes one of the easiest monitors to use.
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Extensive Data Connectivity

Compatible with Infusion/Patient Data Management System
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HL7 communication

Direct HL7-communication allows the exchange of data between the Omya Neonate patient monitor and the hospital information system (HIS) without any additional software.

Technical Specifications

Parameter Specifications

Omya Mainstream CO2 (EtCO2)

• Measurement range:
– 0 mmHg to 150 mmHgIX
• imCO2 measurement range (based on lowest reading over
last 20 seconds): 3 mmHg to 50 mmHg
• Data sample rate: Waveform sampling, 20 samples per second
• CO2 waveform resolution: 0.1 mmHg
• etCO2, imCO2 resolution: 1.0 mmHg
• Initialization time: Full specification etCO2 measurement
displays after warm up, in less than 2 minutes
• Total response time: < 2 seconds
• Calibration interval: No calibration required
• Auto zero interval: Only required when changing the airway
adapter style.
• Accuracy (gas temperature at 35°C):
– ± 2 mmHg in the range 0 to 40 mmHg
– ± 5% of reading in the range 41 to 70 mmHg
– ± 8% of reading in the range of 71 to 100 mmHg
– ± 10% of reading in the range of 101 to 150 mmHg
• Respiration rate range: 0 to 150 rpm
• Respiration rate accuracy: ± 1 rpm
• Drift of measurement accuracy:
– Short term drift (4 hours of use): Does not exceed 0.8 mmHg
– Long term drift (120 hour period): Retains accuracy specification
• Barometric pressure: Configured by system administrator

Omya SpO2

• Measurement range
– SpO2: 0% to 100%
– SpO2 resolution: 1%
– Pulse rate: 30 bpm to 300 bpm
– Pulse rate resolution: 1 bpm
• Pulse rate accuracy: 2% or 1 bpm, whichever is greater
• SpO2 accuracyV (within the range 70% to 100%),
Philips reusable sensors
– ± 2% — M1191B, M1191BL, M1192A,
– ± 3% — M1193A, M1194A, M1195A, M1196A, M1191T, M1192T,
M1196T, M1196S
– ± 4% — M1193T (neonatal)
• SpO2 accuracyV (within the range 70% to 100%),
Philips disposable sensors
– ± 3% — M1131A, M1133A, M1134A (neonatal)
– ± 2% — M1132A, M1133A, M1134A (adult/infant)
• SpO2 accuracyV (within the range 70% to 100%),
Efficia sensors
– ± 3% — 989803160631, 989803160621, 989803160611
• Wavelength rangeVI: 500 nm to 1000 nm for all specified
sensors
• Maximum optical output power: ≤ 15 mW for all specified sensors

Device Application Specifications

Display

Display size:
4.3 inch High-resolution Touchscreen display
Resolution 480 x 272 pixels
Frequency: 50/60 Hz
Viewing Angle: ± 15

Display Screen:
Waveforms,numeric values,on-screen trend data.

Display waveform:
SpO2, Respiration, EtCO2

Numerical data display:
SpO2, pulse rate, temperature, O2 concentration,
FiCO2, EtCO2,

Communication Interfaces

• USB port (complies with the USB 2.0 standard
as a full-speed host), to
– Upgrade software
– Connect to a barcode scanner, or a serial
interface adapter
• Ethernet port, to
– Export HL7 data
– Connect the monitor to the Efficia CMS200 central station
• Wireless connectivityIII
Option E20 enables the monitor to access the EMR using
the customer’s existing wireless infrastructure. The monitor
supports the following wireless standards: IEEE802.11a, 802.11b,
802.11g, and 802.11n, operating in the 2.4 GHz or 5 GHz bands.
• EMR connectivity
– Via LAN
– Via WLAN

Power Supply

Integrated Power Supply,
Rated Voltage :
AC 100~240 V, 50~60 Hz,
Power Consumption :
25 VA
External DC power supply :
12V DC supply

Physical Dimensions

Dimension (H) x (W) x (T) in mm:
152 x  82 x  30.5 mm
Weight :
450g (with clamp base)

Battery

Battery Capacity :
Advanced Rechargeable Lithium Polymer battery –
7.4 V, 4000 mAh (1 Internal battery)

Battery life :
Continuously operate for 6-8 hrs from Full Charge
(at a rate of 5 ml/h at 30°C under Normal Conditions)

Battery Recharge :
When AC Power is ON,
Battery will Automatically Recharge
(about 5 hrs to 90% charge ),
When the pump is off,
the charging time is not longer than 4 hrs

External Fuse

1.5 A / 250 V (User Replaceable)

Environmental Conditions

Operation Conditions:
Ambient temperature: + 5 to + 40°C,
Atmosphere Pressure: 86 ~106 kPa,
Relative humidity: ≤ 80%

Storage Conditions :
Ambient temperature: – 20 to +55°C,
Atmosphere Pressure: 50 ~106 kPa,
Relative humidity: ≤ 95%

 

Mechanical shock
Complies with mechanical shock requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Peak acceleration: 150 m/s2 (15.3 g)
• Duration: 11 ms
• Pulse shape: Half sine
• Number of shocks: 3 shocks per direction per axis (18 total) Mechanical vibration
Complies with mechanical vibration requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Frequency range: 10 Hz to 2000 Hz
• Resolution: 10 Hz
• Acceleration amplitude:
– 10 Hz to 100 Hz: 1.0 (m/s2)2/Hz
– 100 Hz to 200 Hz: -3.0 dB/octave
– 200 Hz to 2000 Hz: 0.5 (m/s2)2/Hz
• Duration: 10 minutes per each perpendicular axis (3 total)
Humidity
• Operating: 15% to 90% RH, non-condensing
• Storage: 15% to 90% RH, non-condensing

Safety Standards and Compliance

Classification & Electrical Safety Protection

Product Classification
According to the MDD 93/42/EEC Appendix Ⅸ Classification Rule 10: class II b

Type of protection against electric shock
Class I, equipment contains an internal powered equipment

Level of protection against electric shock
Application of CF-type non-defibrillation discharging effect protection

EMC type
Group 1, Class A

Anti-electroshock degree
ECG (RESP), TEMP, IBP, C.O., Quick Temp CF, SpO2, NIBP, CO2

Ingress Protection
IPx1 (No protection against ingress of water)

Disinfection/sterilization method
Standard method

Working system
Continuous operation equipment

Power supply way
Grid power plug, removable and soft wire power supply

Visual Alarm Indication

Visual Alarms indicates with two priority colors:
Red (High Priority) and
Yellow (Low and Mid Priority),
meets according to the IEC 60601-1-8 standard requirements.

Safety Standards

EN/IEC 60601-1
EN/IEC 60601-1-2
EN/IEC 60601-1-8
EN/IEC 60601-2-27
EN/ IEC 80601-2-30
IEC 60601-2-34
IEC 60601-2-49
EN/ISO 80601-2-55
EN/ISO 80601-2-61
EN/IEC 62366
EN/IEC 62304
EN/IEC 60601-1-6
EN/ISO 80601-2-56

• Conformity: CE according to directive 93/42/EEC class IIb
• Protection class: Protection against electric shocks, Class I, internally powered equipment, per EN/IEC 60601-1
• Degree of protection: Type CF defibrillator-proof, per EN/IEC 60601-1
• IPX1 Ingress protection against vertically falling water drops, This device is not designed for outdoor use
• Protection against hazards of ignition of flammable anesthetic mixtures:
Equipment is not suitable for use in the presence of a flammable anesthetic mixtures with air or oxygen or nitrous
oxide, per IEC 60601-1
Additional requirements: EN 1060-1, EN 1060-3 and EN 12470-4

Audio Alarm Volume :

Support multi-level volume functions
with the sound pressure range from 59-74 dB(A)
and key pad beep;
The alarm sound meets according to
the IEC 60601-1-8 standard requirements.

General Specifications

Display

Display size:
8″ High-resolution Touchscreen display
Resolution 800 x 600 pixels
Frequency: 50/60 Hz
Viewing Angle: ± 15

Maximum number of waveform display:
7 traces

Display waveform:
ECG (up to 3 leads), Respiration, IBP,
SpO2, pulse wave, CO2,

Numerical data display:
Heart rate, VPC rate, ST level,
respiration rate, IBP (systolic, diastolic,
mean), NIBP (systolic, diastolic, MAP),
SpO2, pulse rate, temperature, CO,
cardiac index, injectate temperature,
blood temperature, O2 concentration,
FiCO2, EtCO2,

Communication Interfaces

• USB port (complies with the USB 2.0 standard
as a full-speed host), to
– Upgrade software
– Connect to a barcode scanner, or a serial
interface adapter
• Ethernet port, to
– Export HL7 data
– Connect the monitor to the Efficia CMS200 central station
• Wireless connectivityIII
Option E20 enables the monitor to access the EMR using
the customer’s existing wireless infrastructure. The monitor
supports the following wireless standards: IEEE802.11a, 802.11b,
802.11g, and 802.11n, operating in the 2.4 GHz or 5 GHz bands.
• EMR connectivity
– Via LAN
– Via WLAN

Power Supply

Integrated Power Supply,
Rated Voltage :
AC 100~240 V, 50~60 Hz,
Power Consumption :
25 VA
External DC power supply :
12V DC supply

Physical Dimensions

Dimension (L) x (W) x (H) in mm:
260 x 138 x 245
Weight :
3.7 kg (with clamp base)

Battery

Battery Capacity :
Advanced Rechargeable Lithium Polymer battery –
7.4 V, 4000 mAh (1 Internal battery)

Battery life :
Continuously operate for 6-8 hrs from Full Charge
(at a rate of 5 ml/h at 30°C under Normal Conditions)

Battery Recharge :
When AC Power is ON,
Battery will Automatically Recharge
(about 5 hrs to 90% charge ),
When the pump is off,
the charging time is not longer than 4 hrs

External Fuse

1.5 A / 250 V (User Replaceable)

Environmental Conditions

Operation Conditions:
Ambient temperature: + 5 to + 40°C,
Atmosphere Pressure: 86 ~106 kPa,
Relative humidity: ≤ 80%

Storage Conditions :
Ambient temperature: – 20 to +55°C,
Atmosphere Pressure: 50 ~106 kPa,
Relative humidity: ≤ 95%

 

Mechanical shock
Complies with mechanical shock requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Peak acceleration: 150 m/s2 (15.3 g)
• Duration: 11 ms
• Pulse shape: Half sine
• Number of shocks: 3 shocks per direction per axis (18 total) Mechanical vibration
Complies with mechanical vibration requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Frequency range: 10 Hz to 2000 Hz
• Resolution: 10 Hz
• Acceleration amplitude:
– 10 Hz to 100 Hz: 1.0 (m/s2)2/Hz
– 100 Hz to 200 Hz: -3.0 dB/octave
– 200 Hz to 2000 Hz: 0.5 (m/s2)2/Hz
• Duration: 10 minutes per each perpendicular axis (3 total)
Humidity
• Operating: 15% to 90% RH, non-condensing
• Storage: 15% to 90% RH, non-condensing

Configuration and Optional Features

Event Log Review

Approximately one year event log of normal use and
Min. 2000 records with time and date

Mounting options

The monitor has the following mounting options:
• Roll stand
• Roll stand mounting kit
• Wall mount
• Wall channel
• Bedrail hook

Wireless LAN (Optional)

Wireless Data Transmission compatible with Patient Data Management Systems (Optional)

Nurse Staff call (Optional)

Max. 24 V / 0,5 A / 24 VA

Parameter Specifications

Parameter Specifications

Omya Mainstream CO2 (EtCO2)

• Measurement range:
– 0 mmHg to 150 mmHgIX
• imCO2 measurement range (based on lowest reading over
last 20 seconds): 3 mmHg to 50 mmHg
• Data sample rate: Waveform sampling, 20 samples per second
• CO2 waveform resolution: 0.1 mmHg
• etCO2, imCO2 resolution: 1.0 mmHg
• Initialization time: Full specification etCO2 measurement
displays after warm up, in less than 2 minutes
• Total response time: < 2 seconds
• Calibration interval: No calibration required
• Auto zero interval: Only required when changing the airway
adapter style.
• Accuracy (gas temperature at 35°C):
– ± 2 mmHg in the range 0 to 40 mmHg
– ± 5% of reading in the range 41 to 70 mmHg
– ± 8% of reading in the range of 71 to 100 mmHg
– ± 10% of reading in the range of 101 to 150 mmHg
• Respiration rate range: 0 to 150 rpm
• Respiration rate accuracy: ± 1 rpm
• Drift of measurement accuracy:
– Short term drift (4 hours of use): Does not exceed 0.8 mmHg
– Long term drift (120 hour period): Retains accuracy specification
• Barometric pressure: Configured by system administrator

Omya SpO2

• Measurement range
– SpO2: 0% to 100%
– SpO2 resolution: 1%
– Pulse rate: 30 bpm to 300 bpm
– Pulse rate resolution: 1 bpm
• Pulse rate accuracy: 2% or 1 bpm, whichever is greater
• SpO2 accuracyV (within the range 70% to 100%),
Philips reusable sensors
– ± 2% — M1191B, M1191BL, M1192A,
– ± 3% — M1193A, M1194A, M1195A, M1196A, M1191T, M1192T,
M1196T, M1196S
– ± 4% — M1193T (neonatal)
• SpO2 accuracyV (within the range 70% to 100%),
Philips disposable sensors
– ± 3% — M1131A, M1133A, M1134A (neonatal)
– ± 2% — M1132A, M1133A, M1134A (adult/infant)
• SpO2 accuracyV (within the range 70% to 100%),
Efficia sensors
– ± 3% — 989803160631, 989803160621, 989803160611
• Wavelength rangeVI: 500 nm to 1000 nm for all specified
sensors
• Maximum optical output power: ≤ 15 mW for all specified sensors

Application Specifications

Device Application Specifications

Display

Display size:
4.3 inch High-resolution Touchscreen display
Resolution 480 x 272 pixels
Frequency: 50/60 Hz
Viewing Angle: ± 15

Display Screen:
Waveforms,numeric values,on-screen trend data.

Display waveform:
SpO2, Respiration, EtCO2

Numerical data display:
SpO2, pulse rate, temperature, O2 concentration,
FiCO2, EtCO2,

Communication Interfaces

• USB port (complies with the USB 2.0 standard
as a full-speed host), to
– Upgrade software
– Connect to a barcode scanner, or a serial
interface adapter
• Ethernet port, to
– Export HL7 data
– Connect the monitor to the Efficia CMS200 central station
• Wireless connectivityIII
Option E20 enables the monitor to access the EMR using
the customer’s existing wireless infrastructure. The monitor
supports the following wireless standards: IEEE802.11a, 802.11b,
802.11g, and 802.11n, operating in the 2.4 GHz or 5 GHz bands.
• EMR connectivity
– Via LAN
– Via WLAN

Power Supply

Integrated Power Supply,
Rated Voltage :
AC 100~240 V, 50~60 Hz,
Power Consumption :
25 VA
External DC power supply :
12V DC supply

Physical Dimensions

Dimension (H) x (W) x (T) in mm:
152 x  82 x  30.5 mm
Weight :
450g (with clamp base)

Battery

Battery Capacity :
Advanced Rechargeable Lithium Polymer battery –
7.4 V, 4000 mAh (1 Internal battery)

Battery life :
Continuously operate for 6-8 hrs from Full Charge
(at a rate of 5 ml/h at 30°C under Normal Conditions)

Battery Recharge :
When AC Power is ON,
Battery will Automatically Recharge
(about 5 hrs to 90% charge ),
When the pump is off,
the charging time is not longer than 4 hrs

External Fuse

1.5 A / 250 V (User Replaceable)

Environmental Conditions

Operation Conditions:
Ambient temperature: + 5 to + 40°C,
Atmosphere Pressure: 86 ~106 kPa,
Relative humidity: ≤ 80%

Storage Conditions :
Ambient temperature: – 20 to +55°C,
Atmosphere Pressure: 50 ~106 kPa,
Relative humidity: ≤ 95%

 

Mechanical shock
Complies with mechanical shock requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Peak acceleration: 150 m/s2 (15.3 g)
• Duration: 11 ms
• Pulse shape: Half sine
• Number of shocks: 3 shocks per direction per axis (18 total) Mechanical vibration
Complies with mechanical vibration requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Frequency range: 10 Hz to 2000 Hz
• Resolution: 10 Hz
• Acceleration amplitude:
– 10 Hz to 100 Hz: 1.0 (m/s2)2/Hz
– 100 Hz to 200 Hz: -3.0 dB/octave
– 200 Hz to 2000 Hz: 0.5 (m/s2)2/Hz
• Duration: 10 minutes per each perpendicular axis (3 total)
Humidity
• Operating: 15% to 90% RH, non-condensing
• Storage: 15% to 90% RH, non-condensing

Safety Standards and Compliance

Safety Standards and Compliance

Classification & Electrical Safety Protection

Product Classification
According to the MDD 93/42/EEC Appendix Ⅸ Classification Rule 10: class II b

Type of protection against electric shock
Class I, equipment contains an internal powered equipment

Level of protection against electric shock
Application of CF-type non-defibrillation discharging effect protection

EMC type
Group 1, Class A

Anti-electroshock degree
ECG (RESP), TEMP, IBP, C.O., Quick Temp CF, SpO2, NIBP, CO2

Ingress Protection
IPx1 (No protection against ingress of water)

Disinfection/sterilization method
Standard method

Working system
Continuous operation equipment

Power supply way
Grid power plug, removable and soft wire power supply

Visual Alarm Indication

Visual Alarms indicates with two priority colors:
Red (High Priority) and
Yellow (Low and Mid Priority),
meets according to the IEC 60601-1-8 standard requirements.

Safety Standards

EN/IEC 60601-1
EN/IEC 60601-1-2
EN/IEC 60601-1-8
EN/IEC 60601-2-27
EN/ IEC 80601-2-30
IEC 60601-2-34
IEC 60601-2-49
EN/ISO 80601-2-55
EN/ISO 80601-2-61
EN/IEC 62366
EN/IEC 62304
EN/IEC 60601-1-6
EN/ISO 80601-2-56

• Conformity: CE according to directive 93/42/EEC class IIb
• Protection class: Protection against electric shocks, Class I, internally powered equipment, per EN/IEC 60601-1
• Degree of protection: Type CF defibrillator-proof, per EN/IEC 60601-1
• IPX1 Ingress protection against vertically falling water drops, This device is not designed for outdoor use
• Protection against hazards of ignition of flammable anesthetic mixtures:
Equipment is not suitable for use in the presence of a flammable anesthetic mixtures with air or oxygen or nitrous
oxide, per IEC 60601-1
Additional requirements: EN 1060-1, EN 1060-3 and EN 12470-4

Audio Alarm Volume :

Support multi-level volume functions
with the sound pressure range from 59-74 dB(A)
and key pad beep;
The alarm sound meets according to
the IEC 60601-1-8 standard requirements.

General Specifications

General Specifications

Display

Display size:
8″ High-resolution Touchscreen display
Resolution 800 x 600 pixels
Frequency: 50/60 Hz
Viewing Angle: ± 15

Maximum number of waveform display:
7 traces

Display waveform:
ECG (up to 3 leads), Respiration, IBP,
SpO2, pulse wave, CO2,

Numerical data display:
Heart rate, VPC rate, ST level,
respiration rate, IBP (systolic, diastolic,
mean), NIBP (systolic, diastolic, MAP),
SpO2, pulse rate, temperature, CO,
cardiac index, injectate temperature,
blood temperature, O2 concentration,
FiCO2, EtCO2,

Communication Interfaces

• USB port (complies with the USB 2.0 standard
as a full-speed host), to
– Upgrade software
– Connect to a barcode scanner, or a serial
interface adapter
• Ethernet port, to
– Export HL7 data
– Connect the monitor to the Efficia CMS200 central station
• Wireless connectivityIII
Option E20 enables the monitor to access the EMR using
the customer’s existing wireless infrastructure. The monitor
supports the following wireless standards: IEEE802.11a, 802.11b,
802.11g, and 802.11n, operating in the 2.4 GHz or 5 GHz bands.
• EMR connectivity
– Via LAN
– Via WLAN

Power Supply

Integrated Power Supply,
Rated Voltage :
AC 100~240 V, 50~60 Hz,
Power Consumption :
25 VA
External DC power supply :
12V DC supply

Physical Dimensions

Dimension (L) x (W) x (H) in mm:
260 x 138 x 245
Weight :
3.7 kg (with clamp base)

Battery

Battery Capacity :
Advanced Rechargeable Lithium Polymer battery –
7.4 V, 4000 mAh (1 Internal battery)

Battery life :
Continuously operate for 6-8 hrs from Full Charge
(at a rate of 5 ml/h at 30°C under Normal Conditions)

Battery Recharge :
When AC Power is ON,
Battery will Automatically Recharge
(about 5 hrs to 90% charge ),
When the pump is off,
the charging time is not longer than 4 hrs

External Fuse

1.5 A / 250 V (User Replaceable)

Environmental Conditions

Operation Conditions:
Ambient temperature: + 5 to + 40°C,
Atmosphere Pressure: 86 ~106 kPa,
Relative humidity: ≤ 80%

Storage Conditions :
Ambient temperature: – 20 to +55°C,
Atmosphere Pressure: 50 ~106 kPa,
Relative humidity: ≤ 95%

 

Mechanical shock
Complies with mechanical shock requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Peak acceleration: 150 m/s2 (15.3 g)
• Duration: 11 ms
• Pulse shape: Half sine
• Number of shocks: 3 shocks per direction per axis (18 total) Mechanical vibration
Complies with mechanical vibration requirement according to ISO 9919/IEC 80601-2-61 standards, for use within the healthcare facility.
Test conditions include:
• Frequency range: 10 Hz to 2000 Hz
• Resolution: 10 Hz
• Acceleration amplitude:
– 10 Hz to 100 Hz: 1.0 (m/s2)2/Hz
– 100 Hz to 200 Hz: -3.0 dB/octave
– 200 Hz to 2000 Hz: 0.5 (m/s2)2/Hz
• Duration: 10 minutes per each perpendicular axis (3 total)
Humidity
• Operating: 15% to 90% RH, non-condensing
• Storage: 15% to 90% RH, non-condensing

Configuration & Optional Features

Configuration and Optional Features

Event Log Review

Approximately one year event log of normal use and
Min. 2000 records with time and date

Mounting options

The monitor has the following mounting options:
• Roll stand
• Roll stand mounting kit
• Wall mount
• Wall channel
• Bedrail hook

Wireless LAN (Optional)

Wireless Data Transmission compatible with Patient Data Management Systems (Optional)

Nurse Staff call (Optional)

Max. 24 V / 0,5 A / 24 VA

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