Rev. 1.4 / 02-16-2017
DP450 Tap Water Iontophoresis System User Manual
23
Symbol Legend / Manufacturer / Device Identification
Caution,
Power Output
Connector for electrodes
+ = Anode , - = Cathode
Shock Protection
Type
Device leakage currents comply with stand-
ards -- the system provides protection against
electrical shock (Type B); device is insulated
(floating) (Type F).
Prescription Use
Only
Federal law restricts this device to sale by or
on the order of a physician.
Indoor Use Only
This treatment device should be used indoors
only and should be kept dry.
Consult Instruc-
tions For Use
Read and understand instruction manu-
al/booklet before you start treatment or using
the device.
Not For General
Waste (EU
States)
This devices is reusable and not contaminated
at end of life (complies with WEEE-Directive
2012/19/EU).
Manufacturer
Hidrex GmbH, Otto-Hahn-Str.12
Heiligenhaus Germany 42579
info@hidrex.de www.hidrex.de
CE Mark, ID# of
Notified Body
Conformity with health and safety require-
ments set out in European Directive 93/42/EU.
UDI (Device
Identification)
Device Identification: 14-digit unique DI# (Gtin)
Serial Number
(part of UDI)
Serial#: yy-x.xxxx (yy: year of manufacture)
Lifespan
Legal reasons limit the lifespan of this medical device to 4 years. The manufac-
turer must recondition the medical device no later than by the end of this term.
Each successful reconditioning by the manufacturer extends the lifespan of the
medical device by 2 years. If the HIDREX tap water iontophoresis system is
reconditioned for the same patient, the treatment trays or carrying case (depend-
ing on their condition) do not necessarily have to be replaced.