Instruction Manual for the Delivery Table FREYA 3
Page 25
The central control panel and side rail control panels should be dry cleaned.
Washing and disinfecting should be performed only when necessary, with as little
liquid as possible.
When cleaning and disinfecting the controller, exercise extreme caution.
Should the controller be spilled over with water, some agents or other fluids, dry it,
and wipe its edges dry with a cloth.
Failure to observe the requirements mentioned above shall render the medical device
warranty null and void.
6.3.
Damage and defects
Damage and defects detected in the medical device or its equipment are to be immediately reported to
a responsible person. The device which cannot be safely operated (defective electrical or mechanical
elements) must not be used until it is fixed.
6.4.
Repairs and maintenance works
Repairs are performed by the manufacturer. The user may not single-handedly perform any repairs of
or introduce any modifications to the device without special training and permit. Having obtained a
written consent of the manufacturer for the repair by the technical customer staff, the manufacturer
shall make available indispensable schematic drawings, indices of parts, descriptions and information
related to the repair.
The manufacturer allows the use of original spare parts only. In order to ensure safe and reliable
operation of the medical device, use only spare parts delivered by the manufacturer. Handling of worn
parts must be compliant with applicable regulations pertaining to the environmental protection.
NOTE!
The device contains products which may pose a threat to the environment:
- gel battery – type EP 1,2-12 - (2 pcs.).
Rules of conduct as regards worn products that may pose a threat to the
environment are specified by regulations pertaining to the environmental
protection.
If the batteries run out, they may be replaced by the manufacturer or qualified
technical staff of the customer, acc. to the replacement manual obtained from the
manufacturer.
Used up batteries are collected by the medical device manufacturer or external
company in possession of business approvals required by the environmental
protection law.
Repairs and maintenance works must be performed only by qualified staff. If operated without
(outside) Poland, the necessity of repairing or servicing the device should be reported to the
manufacturer or dealer from whom the device has been purchased.
All repairs should be registered on the List of repairs, attached to the warranty card of the
device.
6.5.
Technical state inspections and checks
So as to provide safety and proper technical state of the device, the user is obliged to periodically
submit it to technical inspections. These inspections are performed by the manufacturer, at the
expense of the user, or by authorised and qualified technical staff of the customer.
NOTE!
Technical inspections should be registered on the List of repairs, delivered
together with the warranty card of the device.
Only the positive inspection result can constitute the grounds for further device
operation.
After the operation period expires, the permit for further operation is issued, if the
technical inspection result is positive, which inspection is performed by an
authorised service centre. Every time, the permit is issued for 12 months.