Unpacking And Installation; Unpacking And Inspection; Storage - Interacoustics Aqua Stim Instructions D'utilisation

Aqua Stim Water Irrigator Instructions for Use - EN

2 Unpacking and Installation

2.1 Unpacking and Inspection

Check box and contents for damage
When the instrument is received please check the shipping box for rough handling and damage. If the box is
damaged it should be kept until the contents of the shipment have been checked mechanically and
electrically. If the instrument is faulty please contact your local distributor. Keep the shipping material for the
carrier's inspection and insurance claim.
Keep carton for future shipment
The Aqua Stim Water Irrigator comes in its own shipping carton, which is specially designed for the Aqua
Stim Water Irrigator. Please keep this carton. It will be needed if the instrument has to be returned for
service. If service is required please contact your local distributor.
Reporting Imperfections
Inspect before connection
Prior to connecting the product it should once more be inspected for damage. All of the cabinet and the
accessories should be checked visually for scratches and missing parts.
Report immediately any faults
Any missing part or malfunction should be reported immediately to the supplier of the instrument together
with the invoice, serial number, and a detailed report of the problem. In the back of this manual you will find a
"Return Report" where you can describe the problem.

2.2 Storage

Environmental Conditions
Standards Compliance

Class I device for protection against electric shock

Type B Applied Part for degree of protection against electric

IPX0 rating for degree of protection against the ingress of water
(I.e. the system will be damaged if any water is absorbed by the electronic equipment)
The Aqua Stim was tested according to IEC60601-1-2 regarding EMC. Thus, you can install and use the
Aqua Stim in a clinical exam room where other medical equipment is located.
Medical electrical equipment needs special precautions regarding electromagnetic compatibility (EMC) and
needs to be installed and put into service according to the EMC information provided.
 Portable and mobile radio frequency (RF) communications equipment (e.g. cell phones, personal
data assistants, etc.) can affect medical electrical equipment. This equipment should not be used at
close distances to the equipment.
 Power frequency magnetic fields should be at levels characteristic of a typical location in a typical
commercial or hospital environment.
Performance Conditions
Temperature
of Room
Relative Humidity
The Aqua Stim may not be used in rooms where there are explosion risks. The
equipment is not suitable for use in the presence of flammable anesthetic mixtures
with air or oxygen or nitrous oxide.
20°C ~ 30°C
68°F ~ 86°F
Non-condensing
shock
Storage Conditions
Temperature
of Room
Relative Humidity
Page 5
1°C ~ 52°C
33°F ~ 125°F
Non-condensing