Service And Maintenance; Installation; Connection - Enraf Nonius Curapuls 670 Gebrauchsanweisung

apparatus, we refer to the therapy books "Shortwave therapy" and "Pulsed short wave therapy with the
Curapuls 670".
Enraf-Nonius cannot be held responsible for any consequences to the operator or the patient due to faulty
diagnosis, misuse or mishandling of the equipment or its accessories, misunderstanding of the operating
instructions, faulty connection(s) with combined equipment or incorrect interpretation of these operating
instructions. The consequences of incorrect maintenance are also excluded.
The Curapuls 670 meets the requirements of the international standard for the safety of medical electrical
equipment IEC 60601-1 (General standard), IEC 60601-2-3 (Standard for shortwave therapy equipment)
and IEC 60601-1-2 (Standard for EMC). According to the IEC 60601-1-2 (1993) directive, clause
36.201.1.8, class A equipment and/or systems (CISPR 11 Classification) are allowed in domestic
establishments when used under the jurisdiction of a health care professional.
3.2

Service and maintenance

We advise to have the Curapuls 670 checked per service manual test routines and safety tested once
each year at your local authorized service office. It is also recommended that a record be kept of all
activities relating to service and maintenance. In some countries this is even obligatory. The check up
and/or technical maintenance must be carried out conform the procedure described in the service manual
of the unit. Opening of the equipment by an unauthorized agency is not allowed and will cancel the right
of guarantee. The manufacturer will not be held responsible for damage to equipment or injuries to
persons operating or being treated with the equipment that result from service or maintenance performed
by companies or persons not authorized by the manufacturer.
USA ONLY
Safety precautions
This unit operates with high voltages. Servicing of the Curapuls 670 should be referred to qualified
service technicians or returned directly to the distributor. To assure continued compliance with FDA, 21
C.F.R. 1050.10 standards, the Curapuls 670 should be calibrated and safety tested at least once each
year. Enraf-Nonius recommends that all service work be performed by the distributor. However, a service
manual can be obtained by writing the company for those who are qualified to service the device and are
fully aware of their responsibilities.
Caution:
Use of controls, adjustments or procedures other than those specified herein may result in hazardous
exposure to shortwave energy.
3.3

Installation

•
Good air circulation is essential to prevent internal heat build-up.
Do not install the unit in a location near heat sources such as radiators or air ducts, and pre-vent
exposure to direct sunlight.
•
The unit should be installed in such a way, that its warmth can be passed on to the surroundings.
Don't cover the ventilation openings.
•
Furthermore, it is recommended that the Curapuls 670 should not be used after extreme
temperature fluctuations.
•
We advise against using wireless telephones in the vicinity of the unit.
•
When moving or transporting the unit, never pull at the electrodes or the electrode arm, to avoid
the risk of tilting the Curapuls 670.
•
For safety reasons, the brakes on the wheels of the unit should be locked before the beginning of
a treatment.
•
The Curapuls 670 is not intended for use in so-called "wet rooms" (hydrotherapy rooms).
•
Should any liquid or foreign object fall into the cabinet, turn off the power, unplug the unit and
have it checked by your nearest authorized service dealer before any further operation.
3.4

Connection

The Curapuls 670 is a class I, type BF apparatus according to IEC 60601-1. This means that the
Curapuls 670 must be connected to a grounded power supply. Use only the power cable supplied with
the apparatus.
EN
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