getemed VitaGuard VG310, Operating Instructions Manual

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14 Intended use
2 Intended use
This section provides information on the intended use of VitaGuard®
and the limitations of this intended use.
The doctor treating the patient is responsible for the application of
VitaGuard®. The specific “Information for the doctor and qualified
medical staff” can be found on page 78.
getemed AG recommends qualified training for the caregivers in
potentially necessary resuscitation techniques. Clearing the respira-
tory tract and the resuscitation of babies and infants require particu-
lar know-how that the treating doctor should communicate to the
caregivers.
2.1 Label on the back of the device
The device label serves as a
unique identifier for VitaGuard®.
In addition, the label bears im-
portant cautionary information.
On the device label you will
find the manufacturer’s name
and address as well as the
product and model name. The
serial number of your device is
given next to SN.
Fig. 2 Device label on the bottom of the device
2.2 Symbols and warnings
This symbol warns you that failure to observe these op-
erating instructions can cause death or injury to the pa-
tient.