Portable Precision

The OMNI Express® Portable Vital Signs Monitor features a 7-inch touch screen interface designed for efficient patient monitoring in outpatient facilities, emergency response environments, and paced clinical settings. The compact unit supports rapid deployment in tight spaces and during patient transport while maintaining consistent monitoring capability. Manufactured in the United States in an ISO 13485 facility, the device is TAA compliant and CE certified (#0476) for distribution within the European Economic Area.

The monitor supports multiple vital sign parameters including non-invasive blood pressure using SunTech technology, ECG with arrhythmia detection, SpO₂ monitoring with either Masimo or Nellcor technology, temperature measurement, and respiratory rate monitoring. Optional capnography support includes Respironics mainstream or sidestream EtCO₂ modules. The adaptable touchscreen interface allows configuration for various clinical workflows while maintaining compatibility with standard hospital monitoring requirements.

Features

Intuitive Touchscreen Interface
7” touchscreen for quick navigation, patient updates, and access to up to 120 hours of data. Supports multi-lead ECG, displays up to 3 waveforms, includes audio-visual alarms, graphical/tabular trends, quick BP recall, and a rechargeable battery with up to 3 hours of use.
Upgradable Monitoring
Adapts across care settings from general wards to surgical use. Standard monitoring includes NIBP, ECG, motion-tolerant SpO₂, temperature, and respiration rate, with optional End-Tidal CO₂ modules for expanded capability.
Advanced Connectivity
Supports Ethernet and RS-232 with open protocol and HL7 compliance for hospital system integration. Enables remote monitoring of up to 32 devices via Infinium Omniview with data archiving and management.

The Omni Express Capnograph is beneficial in:

Clinical scenarios where EtCO₂ monitoring improves safety.

Pain Management

Suppressed respiratory function can occur during patient-controlled analgesia (PCA). Monitoring End-Tidal CO₂ helps clinicians detect respiratory depression early and intervene before severe complications like coma or cardiac arrest occur.

Minor Procedure Sedation

The American Society of Anesthesiologists recommends monitoring ventilation during sedation through clinical observation and exhaled carbon dioxide monitoring. EtCO₂ provides one of the earliest indicators of respiratory complications.

Sedation Dentistry

The American Association of Oral and Maxillofacial Surgeons recommends continuous monitoring of ventilation during sedation and anesthesia. Monitoring exhaled carbon dioxide ensures adequate breathing during procedures.

Specifications

DISPLAY & SYSTEM
Display	7" color TFT
Resolution	1024 × 860
Waveform Display	2 or 3 waveforms
Waveforms Supported	ECG (I, II, III, aVR, aVL, aVF, V1-V6), PLETH, RESP, EtCO2
Indicators	Alarm indicator, power indicator, QRS beep and alarm sound
Trend Time	30 minutes to 72 hours
ECG
Input	5-lead or 3-lead ECG cable, standard AAMI line
Lead Selection	I, II, III, aVR, aVF, aVL, V
Gain	×0.5, ×1.0, ×2.0
CMRR	>100 dB at 50 Hz or 60 Hz
Frequency Range	0.67 to 40 Hz (+3 dB attenuation)
ECG Channels	7 channels
Sweep Speed	12.5, 25, 50 mm/s
Heart Rate Range	30 to 300 bpm
Accuracy	±1 bpm or ±1%
Alarm Limits	Upper 80 to 400 bpm, lower 20 to 150 bpm
RESPIRATION
Measurement Method	RA-LL impedance
Range	0 to 120 rpm
Accuracy	±3 rpm
Alarm Limits	Upper 6 to 120 rpm, lower 3 to 120 rpm
Sweep Speed	12.5, 25 mm/s
NIBP
Technology	Automatic oscillometric measurement
Cuff Inflation Time	Less than 30 s (0 to 300 mmHg, adult cuff)
Measurement Time	Average less than 40 s
Modes	Manual, Auto, STAT
Auto Interval	2 minutes to 4 hours
Pulse Rate Range	30 to 250 bpm
Measurement Range	Adult/Pediatric SYS 40 to 250 mmHg, DIA 15 to 200 mmHg, Neonatal SYS 40 to 135 mmHg, DIA 15 to 100 mmHg
Resolution	1 mmHg
Pressure Accuracy	Maximum mean error ±5 mmHg, maximum standard deviation 8 mmHg
Overpressure Protection	Adult 280 mmHg, Neonatal 150 mmHg
Alarm Limits	SYS 50 to 240 mmHg, DIA 15 to 180 mmHg
TEMPERATURE
Range	25 to 50 °C
Accuracy	±0.2 °C (25.0 to 34.9 °C), ±0.1 °C (35.0 to 39.9 °C), ±0.2 °C (40.0 to 44.9 °C), ±0.3 °C (45.0 to 50.0 °C)
Resolution	0.1 °C
Channels	1 channel
Alarm Limits	0 to 50 °C, configurable
PULSE OXIMETRY (MASIMO SET)
SpO2 Range	0% to 100%
Resolution	1%
Accuracy	±2% adult or pediatric non-motion, ±3% neonate non-motion, ±3% motion conditions, ±2% low perfusion
Averaging Time	2 to 16 seconds selectable
Sensitivity	Normal, Maximum, APOD
Pulse Rate Range	25 to 240 bpm
Pulse Rate Accuracy	±3 bpm non-motion, ±5 bpm motion
Perfusion Index	0.02 to 20%
EtCO2
Sampling Mode	Sidestream or Mainstream
Technology	Non-dispersive infrared single beam optics, dual wavelength
CO2 Range	0 to 150 mmHg, 0 to 19.7%, 0 to 20 kPa
CO2 Resolution	0.1 mmHg (0 to 69 mmHg), 0.25 mmHg (70 to 150 mmHg)
Respiration Rate	2 to 150 bpm
Response Time	Less than 3 seconds
Inspired CO2 Range	3 to 50 mmHg
POWER
Power Source	External AC power and internal battery
AC Input	100 to 240 VAC, 50 or 60 Hz, 150 VA
Battery	Rechargeable lead-acid FB1223 12 V 2.3 Ah
Operating Time	3 hours typical
Low Battery Operation	10 minutes after first low battery alarm
Charge Time	4 hours
ENVIRONMENTAL
Operating Temperature	5 to 40 °C
Storage Temperature	-20 to 60 °C
Humidity	Operating ≤80%, storage ≤80%
RECORDER (OPTIONAL)
Record Width	48 mm
Paper Speed	25 mm/s
Print Output	3 waveforms with patient information and digital values
PROTECTION
Fuse	T 3.0 A

Diagnostics & Clinical Equiptment