2
2
2.0 General
2.3 For your safety
This
Tracheoport®
was subjected to a thorough quality control
before shipment. Carefully inspect the device immediately
for any signs of damage and check the contents of the car-
ton against the delivery note. In case of transport damages,
please contact immediately the competent sender and carrier.
Return shipment of the unit to the sender (e.g. for repair) is only to be
effected in an undamaged shipping carton.
The
Tracheoport®
has been designed acc. to EC-directions on medi-
cal products 93/42/EEC Annex IX and has been classified as suction
unit of group IIa. The unit is marked with the sign CE 0482. The
validity of the conformity certification expires if the customer himself
or a third party manipulates the appliance, e.g. with modifications
of any kind, by installing non-authorized accessories, removing
danger and information signs as well as in case of inappropriate
applications.
The
Tracheoport®
fully complies with the electro-magnetic imm-
munity requirements of standard IEC 601-1-2/EN 60601-1-2
"Electromagnetic com-patibility - Medical Electrical Equipment".
Electro-magnetic interferences and interactions have thus been
reduced to the minimum.
2.1 Dispatch
2.2 Explanation of symbols
Symbol "Caution: pay attention to operating in-structions"
acc. to DIN 30600 1008, IEC 348
This symbol accentuates information relating to safety
and refers to important details when applying the unit.
Important information on use of this unit.
Protection class II
Degree of protection: type BF (body floating)
Connection to bacterial filter
Follow the general cleaning and servicing terms and change
the filter regularly.
Device ON/OFF
Short-time operation
Charging of battery
2.0 General
2.3 For your safety
This
Tracheoport®
was subjected to a thorough quality control
before shipment. Carefully inspect the device immediately
for any signs of damage and check the contents of the car-
ton against the delivery note. In case of transport damages,
please contact immediately the competent sender and carrier.
Return shipment of the unit to the sender (e.g. for repair) is only to be
effected in an undamaged shipping carton.
The
Tracheoport®
has been designed acc. to EC-directions on medi-
cal products 93/42/EEC Annex IX and has been classified as suction
unit of group IIa. The unit is marked with the sign CE 0482. The
validity of the conformity certification expires if the customer himself
or a third party manipulates the appliance, e.g. with modifications
of any kind, by installing non-authorized accessories, removing
danger and information signs as well as in case of inappropriate
applications.
The
Tracheoport®
fully complies with the electro-magnetic imm-
munity requirements of standard IEC 601-1-2/EN 60601-1-2
"Electromagnetic com-patibility - Medical Electrical Equipment".
Electro-magnetic interferences and interactions have thus been
reduced to the minimum.
2.1 Dispatch
2.2 Explanation of symbols
Symbol "Caution: pay attention to operating in-structions"
acc. to DIN 30600 1008, IEC 348
This symbol accentuates information relating to safety
and refers to important details when applying the unit.
Important information on use of this unit.
Protection class II
Degree of protection: type BF (body floating)
Device ON/OFF
Short-time operation
Charging of battery
Connection to bacterial filter
Follow the general cleaning and servicing terms and change
the filter regularly.
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