Warranty & Service - Huntleigh dopplex Intraoperative Probe Mode D'emploi

• Do not use the Intraoperative Probe in the presence of flammable gases such as anaesthetic agents.
• Do not apply the IOP8 to the patient when using high frequency (HF) surgical equipment. Make sure
when using such equipment, that the IOP8 is not in contact with the patient.
• The Intraoperative Probe (IOP8) and the Probe Adaptor must only be connected to the Multi Dopplex II,
Super Dopplex II, Maxi Dopplex 200, Rheo Dopplex II or Mini Dopplex, manufactured by Huntleigh
Healthcare.
• The Multi Dopplex II, Super Dopplex II, Maxi Dopplex 200, Rheo Dopplex II or Mini Dopplex, when used
with these probes, must only be connected to equipment which complies with EN60601- 1or EN60950.
• Do not use the Intraoperative Probe in the eye.
• This product contains sensitive electronics, therefore, strong radio frequency fields could possibly
interfere with it. This will be indicated by unusual sounds from the loudspeaker in the main unit.
We recommend that the source of interference be identified and eliminated.
• The Intraoperative Probes are delicate and should be handled with care. Do not drop or strike against
hard surfaces. Avoid excessive tension on the probe cable.
• Do not sterilise any part of the Multi Dopplex II, Super Dopplex II, Maxi Dopplex 200, Rheo
Dopplex II, Mini Dopplex or Probe Adaptor (PA8).
• These probes are supplied NON STERILE. Always clean and sterilise before use, in accordance with the
Recommended Cleaning and Sterilisation instructions.
• The Intraoperative Probe is a screening tool to aid the healthcare professional and should not be used in
place of normal vascular monitoring. If there is doubt as to vascularity after using the unit, further
investigations should be undertaken immediately using alternative techniques.
• We recommend that exposure to ultrasound should be kept As Low As Reasonably Achievable -
(ALARA guidelines). This is considered to be good practice and should be observed at all times.
Attention, consult accompanying
documents / Instructions to Use
Huntleigh Healthcare's standard terms and conditions
apply to all sales. A copy is available on request.
These contain full details of warranty terms and do
not limit the statutory rights of the consumer.
Service Returns
There are NO USER SERVICEABLE PARTS inside
the probe adaptor or probe.
If for any reason your IOP8 or probe adaptor is being
returned, please:
1. Contact Service Dept. to obtain authorisation
for the product to be returned.
2. Failure to do this may result in the product
being returned without investigation.
3. Clean and sterilise the product, as described
in the cleaning and sterilisation section.
4. Pack in suitable packing.
5. Attach the decontamination certificate, (or other
written statement declaring that the
product has been cleaned and sterilised), to the
outside of the package.
6. Mark the package "Service Department - IOP8
Probe/Adaptor"
WARNING/CAUTIONS & SAFETY
WARRANTY & SERVICE
Means Attention consult this
manual. Refer to safety section.
UK
For further details refer to the NHS document
HSG(93)26.
For service, maintenance and any questions
regarding this, or any other Huntleigh Healthcare
Dopplex product, please contact:
Huntleigh Healthcare Ltd
Diagnostic Products Division
35 Portmanmoor Road, Cardiff
CF24 5HN UK
Tel : +44 (0)29 20485885
Fax: +44 (0)29 20492520
Or your local distributor.
Manufactured in the UK by Huntleigh Healthcare.
As part of the ongoing development programme,
the company reserves the right to modify
specifications and materials of the IOP8 and
Probe Adaptor without notice.
Dopplex, Huntleigh and 'H' logo are registered
trademarks of Huntleigh Technology Ltd. 2003.
Steris - Steris Corporation, USA
Huntleigh Healthcare 2003
3