Iridex G-Probe, Руководство оператора

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4 G-Probe
®
Device Operator Manual 13105-EN Rev E
Tissue absorption is directly dependent upon presence of pigmentation; therefore, dark
pigmented eyes will require lower energies to obtain equivalent results as compared to light
pigmented eyes.
Always keep the fiber-optic tip / eye interface well irrigated to minimize risk of overheating
and of burning tissue onto fiber face. Significant scleral burns are not typical and may
indicate contamination at the G-Probe tip. Replace immediately. Do not continue to use; a
full thickness or near full thickness burn or sclerostomy may result.
If there is an audible “pop” or “snap” during treatment, this may indicate intraocular tissue
disruption; reduce power and leave the duration unchanged.
CAUTIONS:
US federal law restricts this device to sale by or on the order of a healthcare practitioner
licensed by the law of the State in which he/she practices to use or order the use of the device.
Use of controls or adjustments or performing of procedures other than those specified herein
may result in hazardous radiation exposure.
Do not operate the equipment in the presence of flammables or explosives, such as volatile
anesthetics, alcohol, and surgical preparation solutions.
Turn off the laser before inspecting any delivery device components.
Always handle the fiber-optic cables with extreme care. Do not coil the cable into a diameter
less than 15 cm (6 in).
Keep the protective cap over the fiber-optic connector when the delivery device is not in use.
Follow standard facility procedures for the handling of biohazardous material after each use
of the delivery device.
IRIDEX Corporation Contact Information
IRIDEX Corporation
1212 Terra Bella Avenue
Mountain View, California 94043-1824 USA
Telephone:
(650) 940-4700
(800) 388-4747 (US only)
Fax: (650) 962-0486
Technical Support: (650) 962-8100
techsupport@iridex.com
Emergo Europe
Prinsessegracht 20
2514 AP The Hague
The Netherlands
2797