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1 Important information regarding safe use
55000-00011_002_01 – 1756789 – 2017-09-06
1.6
Delivery
Before installation, check the delivered components for completeness and for any
possible transportation damage.
• To check the delivery, unpack all components and carry out visual inspection.
• The components can be identified on the basis of the order number on the
delivery note and / or the order-specific dimension sheet.
1.6.1
Transportation damage
Damage claims
Claims for damage cannot be accepted unless Trumpf Medical is notified without
delay. In the event of damage during transport or missing components, please send
Trumpf Medical a report containing the following information:
Accompanying documents
• Damage record giving details of damage or defects.
• Primary serial number of the device or system or the serial numbers of the
damaged components,
• Order number (shown on the delivery note and/or the order-specific dimension
sheet)
• Name and address of the customer,
• Consignee.
1.6.2
Return address
Returns
In the event of a return, use the original packaging if possible.
Address returns to:
TRUMPF Medizin Systeme GmbH + Co. KG
Carl-Zeiss-Straße 7–9
07318 Saalfeld
Germany
1.7
Information for users
Note that the device may only be operated by persons who have had the
corresponding instruction.
1.7.1
Training for use of the device
Instruction
Training must be carried out directly at the device by qualified staff of the operator or
by an installer of the device who has been authorised by the manufacturer.
• At the end of the briefing, it must be documented that the user in question has
understood the special operating measures necessary regarding use for the
intended purpose.
1.7.2
Obligation of the user to inform and to inspect
Dealing with problems
The instruction manual must be carefully read before commissioning to prevent
possible injuries and damage to goods.
• Check the functional capability and correct condition of the device before every
application or handover for use.
• While the device is in use, do not fail to comply with the provisions of the
instruction manual.
• Get the information you require from the operator’s technical service or from
Trumpf Medical in the event of specific problems that are not treated in sufficient
detail in this instruction manual.
1.8
Purpose of the device
1.8.1
Identification
Conformity
The manufacturer declares that this product complies with the fundamental
requirements according to MDD Appendix I and documents this by means of the CE
and UL marking.