Seite 13 von 20
DOK-ID: WDX01G02, BE # 5100060
1.
General Information
1.1. Manufacturer
MAVIG GmbH
Stahlgruberring 5
81829 Munich
Germany
Phone
+49 (0) 89 420 96 - 0
Fax
+49 (0) 89 420 96 - 200
info@mavig.com
Web
www.mavig.com
1.2. Operation and Operator
Only appropriately trained personnel may operate, clean and disinfect the product (medical and
radiological technical knowledge in accordance with country specific regulations).
The instructions for use are valid only after a properly conducted first commissioning.
Product must be thoroughly cleaned and disinfected before first use.
1.3. Symbols, Safety and Warning instructions
SAFETY-
RELEVANT
Safety relevant instructions are mandatory and must be followed.
Non-observance could result in injury or death of one or more persons. You
must read and understand these instructions before starting up the systems.
CAUTION
Cautions must be observed, otherwise the device may be damaged or
malfunction. You must read and understand these instructions before
starting up the system.
Not sterilizable
The product cannot be sterilized with ethylene oxide, irradiation, aseptic
processing techniques, steam or dry heat.
1.4. Reporting Requirements according to Regulation (EU) 2017/745
In accordance with the relevant legal regulations, serious incidents that have occurred in
connection with a MAVIG medical device must be reported to MAVIG and to the responsible
national authorities in the country in which the user is active. In this sense, incidents are
reportable if the use of the medical device directly or indirectly led, might have let or might lead
to the death or the temporary or permanent serious deterioration of a patient's, user's or other
person's state of health.