Chattanooga
™
Primera 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 Stimulation
(ETS) should not be used by Patients fitted with demand style cardiac
pacemakers. Please seek advice from your health supervisor.
Patient’s shock protection type: BF (Body floated) Equipment.
Floating isolated applied part. It is only intended for connection to
patient’s skin but has floating input circuits. No connections between
patient and earth.
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
requirements set out in European Directives.
0086 - Notified Body identification (BSI).
The Australian government requires that all imported
or locally produced electrical and electronic equipment
comply with electromagnetic compatibility (EMC) emission
requirements. A compliant product must bear the C-Tick logo.
This product should be kept dry.
IP20
on the
unit
This is an indication for protection against ingress of water and
particulate matter. The mark IP20 on your unit means: your unit is
protected against solid foreign objects of 12.5mm dia and greater. Not
protected against water.
IP02
on the
case
IP02 on the carrying case means: Protected from the ingress of water
droplets from a shower of rain.
Do not dispose in normal dustbin (see page 20 for the disposal
instructions).
REF
