Asskea M30 Plus, Инструкция по эксплуатации

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ENGLISH
1.5 Purpose
1.5.1 Intended use
The ASSKEA secretion aspirator M30
Plus
is
a network-independent, mobile medical aspi-
rator and is used for temporary and primarily
spontaneous aspiration of aspirate from the
trachea.
Typical areas of application are:
• in outpatient and inpatient care,
• in homecare, especially for aspiration in
tracheostomy patients.
1.5.2 Essential functions
• Generation of vacuum (high vacuum)
• Generation of flow (high flow)
1.5.3 Applied parts
The suction tube is an applied part of type BF.
1.5.4 Indications
• Tracheostomy patients
• Aspiration on impaired respiratory function
• Aspiration of blood, secretion and food re-
sidues from the oral cavity, the pharyngeal
zone and the bronchial system
• Evacuation of vacuum mattresses and va-
cuum splints
1.5.5 Contraindications
The ASSKEA secretion aspirator M30
Plus
is
contraindicated for the following applica-
tions:
• Liposuction
• Gynecology applications
• Dental applications
• Thoracic drainage
• Continuous drainage
• Applications in wound areas
1.5.6 Restrictions on use
• In medical rooms where potential equaliza-
tion is required (e.g. heart surgery)
• In hazardous areas/ in the MRI environment
• Outdoors/during transport
1.6 Basic safety instructions
–
ATTENTION!
Warning of damage due to improper power
supply
Improper operation causes excess voltage in
the device, which may be transmitted to the
operator.
• Ensure prior to start-up that the mains sup-
ply for connecting the ASSKEA secretion
aspirator M30
Plus
is suitable at 100 V to 240 V
AC with a mains frequency of 50-60 Hz.
• Ensure prior to start-up in UL listed markets
such as the USA or Canada that the mains
supply is designed for a supply voltage of
120 V AC.
• Use only the supplied power supply unit
(type: GTM91099-6015-3.0-T2) with the
ASSKEA secretion aspirator M30
Plus
.
Risks associated with use in conditions that
are not approved
• The device is not intended to be used out-
doors / during transport.
• The device is not intended to be used in
medical rooms where potential equalizati-
on is required (e.g. heart surgery).
• The device is not intended to be used in ha-
zardous areas / in the MRI environment.