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SoundCare™ Plus Pain Relief Device
15.
NORMALZED
SYMBOLS
Manufacturer’s name and address
Date of manufacture
Type BF Applied Part
SN
LOT
Serial Number of product
Batch code
Caution: Attention, see instructions for use
Disposal in accordance with Directive
2002/96/EC (WEEE)
IPX7
0123
Only for treatment head: Protected against the effects of
temporary immersion water
Complies with the European Medical Device
Directive (93/42/EEC)
Notified body is TUV SUD(0123)
The electrical safety meet the CB system requirements
Indoor use only
Risk of electric shock
E230351
Complies with the safety requirements of Canada and U.S.
The certification body is UL, the cerificate number is E230351
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