NeuroTrac
®
Sports XL 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
tted with
demand style cardiac pacemakers. Please seek advice from
your health supervisor.
Patient’s shock protection type: BF (Body Floated) Equip-
ment. This equipment is not earthed but contains a battery
within an insulated unit.
Indicates the manufacturer’s catalogue number so that the
medical device can be identi
ed.
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.
0123 - Noti
ed body identi
cation.
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 26 for the dispos-
al instructions).
REF
NeuroTrac
®
Sports XL Operation Manual
35
Warranty
Verity Medical Ltd. provides a warranty to the original purchaser that
this product will be free from defects in the material, components and
workmanship, for a period of 2 years from the date of purchase by the
distributor [invoice date from Verity Medical to the appointed distributor].
If the distributor - from whom the product was purchased by the user - is
satis
ed that the product is defective, the user may return the unit directly to
this distributor who will forward it to Verity Medical Ltd. All such returns
from the distributor to Verity Medical must be authorised by Verity Medical
Ltd., in advance. The liability of Verity Medical Ltd., under this limited
product warranty does not extend to any misuse or abuse such as dropping
or immersing the unit in water or other liquid substance or tampering with
the unit or normal wear and tear. Any evidence of tampering will nullify this
warranty.
Customer Service:
Please contact your distributor for any customer service enquiries, including
the warranty returns.
Your invoice of purchase and/or the rear cover of this manual should state the
name and the contact details of your distributor.
For assistance, if needed, in setting up, using or maintaining the unit, or report
unexpected operation or events, please visit the manufacturer’s website for
further details: www.veritymedical.com.
Manufactured by:
Verity Medical Ltd.
Churchtown House
Tagoat
Co. Wexford, Y35 XY44
Ireland
Tel:
+353 (0) 53 913 2433
+44 (0) 1794 367 110
Fax:
+353 (0) 53 913 2430
+44 (0) 1794 367 890
This product is manufactured by Verity Medical Ltd.,
in compliance with the European Union Medical Device Directive
MDD93/42/EEC under the supervision of TÜV SÜD Product Service
GmbH Zerti
zierstellen,
Noti
ed Body number 0123.
Verity Medical Ltd. is certi
ed by Lloyd’s Register Quality Assurance
Limited to the ISO13485:2016 Quality Standard.