NeuroTrac
®
MultiTENS Operation Manual
2
Symbols on the unit and case
Caution! (electrical output).
Follow operating instructions! Failure to do so could place the
patient or operator at risk.
Neuromuscular Stimulation (STIM) and EMG Triggered Stimula-
tion (ETS) should not be used by Patients fitted with demand style
cardiac Pacemakers. Please seek advice from your health supervi-
sor.
Patient’s shock protection type: BF (Body Floated) Equipment.
This equipment is not earthed but contains a battery within an
insulated unit.
REF
Indicates the manufacturer’s catalogue number so that the medical
device can be identified.
Manufacturer’s LOT/Batch number. Present it together with SN
number when you report a technical fault or claim a warranty
return.
Manufacturer’s serial number of the unit. Present it together with
LOT number when you report a technical fault or claim a warranty
return.
Name and address of Manufacturer.
Date of manufacture.
Conformity indication with the essential health and safety require-
ments set out in European Directives.
0088 - Notified body identification.
This product should be kept dry.
IP20
on the
unit
This is an indication for protection against ingress of water and
particulate matter. This mark means your unit is protected against
solid foreign objects of 12.5mm diameter and greater. Not protected
against water.
IP02
on the
case
This is an indicaion that the case is protected from the ingress of
water droplets from a shower and/or rain.
Do not dispose in normal dustbin (see page 14 for the disposal
instructions).
