Armstrong Medical AquaVENT FD140, Инструкция по эксплуатации

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The device operates as described in these instructions for use,
enclosed documents and on equipment labelling, provided that it
is assembled, operated, maintained and repaired according to the
enclosed documentation. The device must be inspected at regular
intervals. The device must not be used if found to be defective.
Damaged, missing, clearly worn out, warped or contaminated
parts must be replaced immediately. If a repair is necessary, the
manufacturer and distributor recommend requesting advice via
telephone or in writing from the nearest regional service centre.
Maintenance and repairs must only be carried out at the service
centre or by specialists authorised by the manufacturer. The user
of the device shall have sole responsibility for any malfunction or
damage which is due to improper use, poor maintenance,
improper service, improper repairs or modifications carried out by
unauthorised persons.
The devices are provided with serial numbers. Their code system
includes the product group code, year of manufacture and
ascending production number for unique identification.
75XX1234
XX represents a number which indicates the year of
manufacture:
15 = 2015, 16 = 2016, etc.