FujiFilm SonoSite Edge II User Manual page 188

Table 9-5: Labeling symbols (continued)
Symbol Definition
Reading the accompanying documentation is necessary for safe operation of the
medical device
Manufacturer, or Manufacturer and date of manufacture
Authorized representative in the European Community
Alternating Current (AC)
Class 1 device indicating manufacturer's declaration of conformance with Annex VII of
93/42/EEC
Class 1 device requiring verification by the Notified Body of sterilization or
measurement features, or to a Class IIa, IIb, or III device requiring verification or
auditing by the Notified Body to applicable Annex(es) of 93/42/EEC
Attention, refer to the user guide
Device complies with relevant Australian regulations for electronic devices.
Batch code, date code, or lot code type of control number
LOT
Biological risk
Device complies with relevant Brazilian regulations for electro-medical devices
Canadian Standards Association. The "C" and "US" indicators next to this mark signify
that the product has been evaluated to the applicable CSA and ANSI/UL Standards,
for use in Canada and the US, respectively.
9-22 Safety