10
1 Important information regarding safe use
55000-00012_002_01 – 1695233 – 25/01/2018
1.4
Information for operators
Procedural guidelines
The device has been manufactured with state-of-the-art technology and is
operationally safe.
• The device can nevertheless be a source of danger, especially when it is operated
by inadequately trained personnel or used incorrectly or for an unintended
purpose.
• The device may only be operated, cleaned, disinfected and maintained by users
that were trained by specialised staff.
1.4.1
Initial commissioning
Validity
This instruction manual is only valid after successful initial operation by an installer
authorised by the manufacturer.
• A full electrical safety test is required before initial commissioning.
• The operator must be instructed in the operation of the lighting system in
accordance with the applicable instruction manual.
• Prior to being used for the first time, the device must be thoroughly cleaned and
disinfected.
• Once the device has been released for use, the information in this instruction
manual will be binding for the user.
1.4.2
Availability of the instruction manual
Obligation to inform
The instruction manual is part of the device and must therefore be kept in a place in
the immediate vicinity of the device to allow consultation regarding safety
instructions and important operating information at any time.
• Never hand the device to third parties without the valid instruction manual.
Ensure that the instruction manual provided with the device is valid by checking
the identity and version number.
1.4.3
Exclusion of liability
Exclusion of liability
The warranty for the product by Trumpf Medical requires that:
• the device is exclusively used for the proper use and is operated and maintained
in accordance with the provisions of this instruction manual,
• only original spare parts or accessories approved by Trumpf Medical are used,
• no design modifications are made to the device,
• inspections and maintenance work are carried out at the time intervals specified,
• an initial commissioning is carried out and the device is released for operation
with a handover declaration.
1.4.4
Maintenance and repair
The device or parts thereof may only be maintained or repaired by:
• Technical customer service,
• authorised service companies trained by Trumpf Medical,
• the operator's service personnel when trained and authorised by Trumpf
Medical.
After every maintenance or repair event, an electrical safety test must be performed.
1.4.5
Service life of the device
• Trumpf Medical products are designed in compliance with all safety and
maintenance requirements for a service life of 10 years.
• This lifespan includes the functionality of the product when used according to the
specifications in the instruction manual, a guaranteed service and the supply
with spare parts.
• Trumpf Medical applies a quality management system certified in accordance
