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Use
r’s
Manual of OMNI Express Patient Monitor
- 61
037.007.0001 Rev.2
devices for display of real time and derived monitoring data of CO
2
, N
2
O,
and the anesthetic agents Halothane, Enflurane, Isoflurane, Sevoflurane and Desflurane.
It is intended to be connected to a patient breathing circuit for monitoring of
inspired/expired gases during anesthesia, recovery and respiratory care. It may be used in
the operating suite, intensive care unit, patient room and emergency medicine settings for
adult, pediatric and infant patients.
It is not intended to be used as the only means of monitoring a patient. It shall always be
used in combination with other vital signs monitoring devices and/or professional human
judgments of patient condition. The IRMA probe is intended to be used by trained and
authorized health care professionals only.
SAFETY
WARNINGS
⚫
DO NOT use the IRMA Adult/Pediatric airway adapter with infants as the adapter
adds 6 ml dead space to the patient circuit.
⚫
Replace the adapter if rainout/condensation occurs inside the airway adapter.
⚫
Use only PHASEIN manufactured IRMA airway adapters.
⚫
DO NOT use the IRMA Infant airway adapter with adults as this may cause excessive
flow resistance.
⚫
The IRMA probe is not intended to be in patient contact.
⚫
Incorrect probe zeroing will result in false gas readings.
⚫
The IRMA probe is intended for use by authorized and trained medical personnel
only.
⚫
The IRMA probe must not be used with flammable anesthetic agents.
⚫
Disposable IRMA airway adapters shall not be reused. Reuse of the single use
adapter can cause cross infection.
⚫
Used airway adapters shall be disposed of in accordance with local regulations for
medical waste.
⚫
The IRMA probe is intended only as an adjunct in patient assessment. It must be
used in conjunction with other assessments of clinical signs and symptoms.
⚫
DO NOT place the IRMA airway adapter between the endotracheal tube and an
elbow as this may allow patient secretions to block the adapter windows and result in
incorrect operation.
⚫
To keep secretions and moisture from pooling on the windows, always position the
IRMA probe in a vertical position with the LED pointing upwards.
⚫
DO NOT use the IRMA airway adapter with metered dose inhalers or nebulized
medications as this may affect the light transmission of the airway adapter windows.
SYSTEM ASSEMBLY INSTRUCTION
SET-UP
1. Plug the IRMA connector into the Patient Monitor EtCO
2
/Gas socket and switch the
power on.
2. Snap the IRMA probe on top of the IRMA airway adapter. It will click into place when
properly seated.
[
CAUTIONS
]:
⚫
Never sterilize or immerse the IRMA probe in liquid.
⚫
DO NOT autoclave the devices as this will damage them.
⚫
DO NOT apply tension to the sensor cable.
⚫
DO NOT operate the device outside the temperature environment
⚫
(U.S.): Federal law restricts this device to sale by or on the order of a physician.