MIRI
®
II-12 Multiroom IVF incubators User Manual Rev. 4.0
73
Please refer to the "18 pH measuring" section for more information on performing pH
calibration.
37 The Maintenance guide
Your MIRI
®
II-12 multiroom IVF incubator from Esco Medical contains high precision quality
components. These components are chosen to ensure the high durability and performance
of the equipment.
However, continual validation of the performance is necessary.
User validation should be done as a minimum according to instructions given in the "33 The
Validation guide" section.
If problems are encountered, contact Esco Medical or your local representative.
However, to sustain the high-performance level and avoid system errors, the owner is
responsible for having a certified technician who performs components replacements
according to table 37.1.
These components must be replaced in the time intervals specified below. Failure to follow
these instructions may, in the worst-case scenario, result in damage to the specimens in the
incubator.
Warranty void if service intervals are not followed according to table 37.1.
Warranty void if non-original parts are used or non-trained and non-authorized
personnel carry out the servicing.
