Guarantee conditions. Gima 33520, 33519
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Spirolab
User manual
GUARANTEE CONDITIONS
The spirolab device and authorized accessories are guaranteed for a period of:
12 months in the case of professional use (doctor, hospital, etc.)
24 months where the product has been purchased by a patient for private use.
The guarantee takes effect from the date of purchase shown on the invoice or other document.
The guarantee period starts from the date of sale that must be confirmed by an invoice or sales receipt.
The product must be checked at the time of purchase or upon receipt and the manufacturer must be informed immediately of any complaints.
The guarantee covers repair, or (at the manufacturer's discretion) replacement of the product or defective components without any cost for labour or spare parts.
The batteries and components subject to wear and tear, including the reusable turbine, are excluded from the terms of this guarantee.
At the manufacturer's discretion, the guarantee does not apply to the following cases:
Uses that are incorrect, improper or do not conform to the technical or safety standards in force in the country where the product is being used.
Use of the product for purposes that differ from those in the Instructions for Use or failure to observe such instructions.
Repair, adaptation, modification or manhandling by personnel who have not been authorised by the manufacturer.
Damage caused by a lack of or by incorrect maintenance
Damage caused by physical or abnormal electrical stress
Damage caused by faults in the electrical systems or in items of equipment to which the device has been connected.
Series number modified, erased, removed or obliterated.
The repairs and replacements mentioned in the guarantee take place on goods that have been returned to our authorised service centres. For further information about service centres, please contact your local distributor or the manufacturer.
The customer is responsible for the costs incurred for shipping, customs and the delivery of goods.
Every product or component part thereof sent for repair must be accompanied by a clear and detailed explanation of the fault. If the product or component part thereof is to be sent to the manufacturer, this must be authorised in writing or by phone beforehand by the manufacturer.
MIR Medical International Research reserves the right to replace the product or make any changes to it that the company deems necessary.
Rev.1.3 Page 32 of 34
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