Hill-Rom Trumpf Medical TruLight 1000, Инструкция по эксплуатации

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1 Important information regarding safe use
55000-00012_002_01 – 1695233 – 25/01/2018
with DIN EN ISO 13485 for all company processes.
• This guarantees:
– Top quality,
– Easy operation,
– Functional design,
– Optimisation for the intended purpose.
1.4.6 Date of manufacture
The device label indicates the date of manufacture of the device. The position of the
device label on the device is shown in Chapter 4.1.
1.5 Delivery
Before installation, check the delivered components for intactness and for any
possible transportation damage.
• To check the delivery, unpack all components and carry out visual inspection.
• The components can be identified by the order number on the delivery note and/
or the order-specific dimension sheet.
The following applies to Japan: The mains connection wiring may only be used with
the equipment supplied.
1.5.1 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 / 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.
1.5.2 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
1.6 Information for users
The device may only be operated by persons who have undergone appropriate
training.