TIM MIRUS Controller, Инструкция по эксплуатации, Страница: 6 / 68

1 Introduction
6 IFU, MIRUS Controller, en-GB, N.00
1 Introduction
1.1 Intended use
The MIRUS Controller is part of the MIRUS System. It is intended to be used for the application
of volatile anaesthetic agents to humans with a tidal volume of
≥ 200 mL.
1.2 Intended purpose
The MIRUS Controller is designed to work only in combination with the MIRUS Reflector. For
hygiene safety reasons connection of the MIRUS System to a patient is only possible via the
MIRUS Filter.
Note: For more information about the MIRUS Reflector and the MIRUS Filter please refer to
the manufacturer’s IFU.
1.3 C
ontraindication
s
Do not use the MIRUS System with

patients requiring less than 200 mL tidal volume.

patients that have a contraindication for the application of volatile anaesthetic
agents.

pure spontaneously breathing patients without a ventilator securing apnoea
back up ventilation mode.

jet or high frequency ventilation.

leaking patient airway systems, such as face mask or helmet systems.

additional filters (HME/F) or tubes that significantly increase dead space.

active humidification.

low flow anaesthesia.
1.4 MIRUS System
The MIRUS System consists of three devices:

MIRUS Controller (MC)
The electrical device that contains the anaesthetic agent and controls the agent
delivery.

MIRUS Reflector (MR)
The multi patient device connected to the MIRUS Controller, inserted into the
patient’s breathing system.

MIRUS Filter (MF)
The single patient device connected to the MIRUS Reflector, protecting the patient
and breathing system.