pajunk MultiStim ECO, Инструкция по эксплуатации

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General information
The devices are manufactured in accordance with globally applicable guidelines
for hazardous substances.
BF-type application part
Dispose of all components and materials sorted and in an environmentally
friendly way or have them recycled. If the medical device is no longer used, it
must be disposed of according to the country-specific environmental regula-
tions.
Any serious incident that has occurred while using the device should be
reported to the manufacturer and the corresponding authorities of the country
the user and/or patient are residing in.
PAJUNK® GmbH Medizintechnologie, Karl-Hall-Strasse 1, 78187 Geisingen,
Germany.
Key to symbols used in labelling
Manufacturer Consult instructions for use
Catalogue number
Rx
only
Dispensing with prescription only
(The product may only be used
by qualified medical staff for the
intended purpose.)
Do not use if package is damaged
Keep dry
Do not dispose of with domestic
waste
Humidity limitation Advice
Caution Information
Protection against electric shock, type
BF
Product is in conformity with the
applicable requirements set out
in Community harmonization
legislation and is monitored by a
notified body
Date of manufacture
Batch code
Non-sterile
Consult instructions for use (SO
7010-M002)
Keep away from sunlight Quantity
Temperature limit Translation
Pressure range Medical device
Eng
lish