Weinmann MEDUVENT Standard User manual

MEDUVENT Standard User Training © WEINMANN
MEDUVENT Standard
Ventilate
Wherever You Go

MEDUVENT Standard
Device training for user instruction
(including the options: SIMV, S-IPPV)

The aim of this presentation
• Convey extensive product knowledge for safe operation of MEDUVENT
Standard by the user
• Convey extensive product knowledge about pre-sets made on MEDUVENT
Standard by the operator
This training document does not replace the instructions for use.
Technical modifications reserved.
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Contents
• Introduction
•Safety
• Product description
•Preparation and operation
• Description of the modes
• Hygienic reprocessing
• Function check
• Alarms and faults
• Maintenance
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Introduction
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Intended purpose
Emergency and transport ventilator for invasive and non-invasive ventilation via
the nose, mouth and trachea.
àMEDUVENT Standard is used in the treatment of infants, children, and
adults with a body weight of 7 kg and more
àTidal volumes (volume-controlled) of 50 ml or more are possible
àWith monitoring functions for the monitoring of respiratory values
àFor non-invasive ventilation (NIV)
àFor ventilation during CPR
àAlso suitable for gentle ventilation of anesthetized patients (TIVA: total
intravenous anesthesia)
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Areas of application
• Emergency
-For resuscitation at the site of an emergency
-For supporting the induction of anesthesia (TIVA: total intravenous anesthesia)
• Transport
-In ground, sea and air emergency medical service
-Between hospital rooms and departments
-Between the hospital and other premises (secondary transport)
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Exclusions and limitations
• The device has not been approved for the following applications:
- Operation in hyperbaric chambers
- Operation in conjunction with MRI, NMR, NMI
- Use in long-term ventilation for longer than 24 hours
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Contents
• Introduction
•Safety
• Product description
•Preparation and operation
• Description of the modes
• Hygienic reprocessing
• Function check
• Alarms and faults
• Maintenance
MEDUVENT Standard User Training © WEINMANN SKR 11/2019

Safety
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Safety
• Read the instructions for use carefully.
• The Instructions for Use are an important part of the product
• The Instructions for Use must always be kept accessible for every user
• Only use the device for the intended purpose
• Please note that the following safety information is not complete. The
complete safety information can be found in the Instructions for Use!
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Safety
Hazardous therapy as a result of inadequate
patient monitoring!
If the patient and the device are not observed and monitored during
ventilation, delayed responses by medical personnel to alarms and
malfunctions might result in serious or life-threatening injury to the patient
and incorrect therapy.
àContinuously observe and monitor the patient and device during
ventilation.
àAdditionally use external monitoring (e.g. SpO2and/or etCO2)
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Safety
Hazardous therapy due to leaks during
ventilation!
The measured MVi value indicates the volume the device is administering
to the patient. In the event of leaks during ventilation, the measured MVi
value will not match the tidal volume actually administered. If this is not
observed, the patient might suffer serious or life-threatening injury.
àDo not use the measured MVi value as an adequate means of
assessing ventilation.
àUse external monitoring (etCO2or expiratory volume measurement).
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Safety
Disrupted or failed therapy due to use of
bubble humidifiers!
Using bubble humidifiers might cause moisture at the oxygen inlet and
result in malfunctions and device failure.
This might expose the patient to the risk of serious or life-
life-threatening injury.
àDo not use bubble humidifiers.
Disrupted or failed therapy due to incompatibility of
the device with consumables, accessories and other
medical devices!
Defective or non-approved accessories might cause malfunctions,
increased electromagnetic interference or reduced electromagnetic
immunity of the device, incorrect output values, and reduced ventilation
performance. This might expose the patient to the risk of serious or life-
threatening injury.
àOnly use approved accessories.
àFollow the instructions for use for the accessories.
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Safety
Risk of infection resulting from failure to use hygiene filter!
If the device is used without a hygiene filter in a contaminated
environment, it might draw in contaminated ambient air.
This might expose the patient and the user to the risk of serious or life-
threatening injury.
àAlways use a hygiene filter when operating the device in a
contaminated environment.
Risk of infection and contamination from contaminated disposables!
Reused disposables may cause infections and contamination if they come
into contact with airways. This might expose the patient and the user to
the risk of serious or life-threatening injury.
àDo not reuse disposables.
àDo not subject disposables to hygienic reprocessing.
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Safety
Disrupted or failed therapy due to incorrect use
of disposables!
Reusing and reprocessing disposables might induce unpredictable
reactions as a result of aging, embrittlement, wear, thermal loading and
chemical action. This might place the functionality and safety of the
device at risk, and cause the patient or user to suffer serious or life-
threatening injury.
àDo not reuse disposables.
àDo not subject disposables to hygienic reprocessing.
Risk of injury resulting from condensation in the patient valve at
temperatures below 0 °C!
If patients are subjected to sustained ventilation, at temperatures
below 0 °C, the exhalation moisture in the patient valve might
condense and impair the function of the parts. This might expose the
patient to the risk of serious or life-life-threatening injury.
àQuickly move the patient to a warmer location.
àAt temperatures below 5 °C, use a breathing system filter to extend
application time.
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN

Contents
• Introduction
•Safety
• Product description
•Preparation and operation
• Description of the modes
• Hygienic reprocessing
• Function check
• Alarms and faults
• Maintenance
MEDUVENT Standard User Training © WEINMANN SKR 11/2019

SKR 11/2019 MEDUVENT Standard User Training © WEINMANN
Product description

Product description
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN
Display
Alarm light
Display of:
- Power supply
- Battery status

Product description
SKR 11/2019 MEDUVENT Standard User Training © WEINMANN
Oxygen inlet
Measuring circuit
connection
Accessories
connection
Ventilation hose
connection