18
19
Air pressure, humidity and temperature limits for
storage
Disposal
In accordance with Directive 2012/19/EU(WEEE)
Type of protection against electric shock
Class II Equipment
Only for treatment head:
Protected against the effects of temporary immersion water
Complies with the European Medical Device Directive
(93/42/EEC), amended by directive 2007/47/EC
and 2011/65/EU requirements. Notified body TUV
Rheinland (CE0197)
Consult instructions for use
Mode
Time
0197
Symbols
IPX7
Symbols
Model or type designation/order number
Directive 93/42EEC Annex 1,13,3(a) IEC 60601-1(6.1f)
EN ISO 15223-1:2012
Classification electrical
Device: Type BF
IEC 60601-1(6.1l)
Serial number is on the underside of the device and on
the packaging
Directive 93/42EEC Annex 1,13,3(d)
EN 15223-1:2012
Lot Number including year (YY) and Month (MM) of manufacture
CONTRAINDICATIONS: This describes situations where you
should not use REVITIVE Ultrasound
CAUTION: This highlights warnings and cautions when using the
device. Make sure you understand these before using REVITIVE
Ultrasound
Center Positive Polarity
DANGER
Electric shock risk
Energy Efficiency Grade
Indoor use only
Complies with the European Union Directive
2011/65/EU (Hazardous Substances)
Legal manufacturer of device
EU/EC European Authorised Representative
XXXXXXXX
SN
IV
RoHS
REF UT1033
YYMMXXXX
LOT
-10 °C
50 °C
20 %
93 %
1060 hPa
700 hPa
3269_IFU02_14269060.indd 18-19 24/07/2017 11:59
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