G. Heinemann Medizintechnik GmbH
MODULA Paris
User`s manual MODULA Paris (HM_TK_GA-Paris_28062013_06_EN)
1 General notes for usage
The MODULA treatment unit may only be used by persons offering a guarantee of correct usage of the
device and who have been instructed in its use. Instruction may only be given by authorized G. Heinemann
Medizintechnik GmbH personnel.
As for all highly developed technical devices, care and regular maintenance of the treatment unit is very
important. You should also ensure that you are thoroughly familiar with the functions and specifications of
the device.
Caution! Before using the device in actual practice, it is essential that you thoroughly
familiarise yourself with the functions of the treatment unit.
Should you require further information, please contact our sales and service office. Telephone: +49 4191-
95379-0
Caution! G. Heinemann Medizintechnik accepts no liability for the safety or proper
function of the device where it has been installed, extended or repaired by persons who
have not been authorised by the manufacturer or if the device is used incorrectly or other
than as described in the operating instructions.
1.1 Purpose of the device
The product is a Class IIa medical device as defined by Directive 93/42/EEC. The product is to be used for
human medical purposes only. The product consists of a metal body and additional options.
The treatment unit is intended for diagnosis and treatment of ENT conditions. Depending on the equipment
installed, the unit may include ear irrigation, compressed air, suction and cold light.
Operation of the unit requires a power supply and, depending on the equipment installed, water and
drainage connections. Specifications for these can be found in appendix.
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