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Manufacturer
Xavant Technology (Pty) Ltd
Unit 102, The Tannery Industrial Park,
309 Derdepoort Rd,
Silverton, Pretoria, South Africa, 0184
Tel: +27 (0) 12 743 5959
E-mail: support@xavant.com
Web: www.xavant.com
Authorised
Representatives
Emergo Europe
Westervoortsedijk 60,
6827 AT Arnhem
The Netherlands
MedEnvoy Switzerland
Gotthardstrasse
6302 Zug
Switzerland
Europe
MedEnvoy
Prinses Margrietplantsoen 33
Suite 123
2595 The Hague, The Netherlands
Switzerland
Anandic Medical Systems AG
Stadtweg 24,
CH-8245, Feuerthalen - Schweiz
Indications for use
This product is a nerve stimulation device designed to be used by an anaesthetist during
• General Anaesthesia, for the purpose of establishing the efficacy of a Neuromuscular
Blocking Agent using non-invasive surface electrodes (NMS450X+).
• Regional Anaesthesia for the purpose of:
• Nerve mapping using the non-invasive Nerve Mapping Probe (supplied).
• Nerve locating using invasive electrodes/needles (not supplied).
Contraindications
• Infection of the puncture site.
• Known neurological disorders.
• Severe coagulation disorders.
Warnings
• Read the entire User Manual before attempting to use the device.
• Use of cables or accessories other than those supplied with the STIMPOD may result in
serious injury.
• Maintenance on this device may only be performed by the manufacturer or persons
explicitly authorized by the manufacturer.
• Do not use the STIMPOD in close proximity to equipment that produces strong
electromagnetic fields, such as high frequency surgical equipment. The cable leads
could act as antennae and dangerous currents could be induced as a result.
• Do not apply the STIMPOD to patients with implanted electrical devices, such as cardiac
pacemakers, without first consulting with an appropriate medical specialist.
• The device should not be used adjacent to or stacked with other equipment and that if
adjacent or stacked use is necessary, the device should be observed to verify normal
operation in the configuration in which it will be used.
• The patient should avoid contact with metallic objects that are grounded, produce an
electrical conductive connection with other equipment and/or enable capacitive coupling.
• The cables should be positioned in such a way that they do not contact either the patient
or other cables.
• Simultaneous connection of a patient to high frequency surgical ME equipment and the
STIMPOD may result in burns and possible damage to the stimulator.
• Operation in close proximity (e.g. 1m) to a shortwave or microwave therapy ME equipment
may produce instability in the stimulator output.
• Application of electrodes near the thorax may increase the risk of cardiac fibrillation.
Sponsors
Australia
Teleflex Medical Australia
Level 4, 197 Coward St
Mascot NSW 2020
Australia
Caution
Federal (US) law restricts this device to
sale by or on the order of a physician.
Applicable Software
Versions
STIMPOD V10.6 or higher.
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