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Verfügbare Sprachen
Verfügbare Sprachen
Cryomatic MKII Cryosurgical console by KEELER
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Usage of this device for Ophthalmic surgery(s) using cryotherapy (dependent on the
type of surgery being performed) may lead to the following complications / side effects,
such as transient conjunctival edema, eyelid edema, meibomian gland dysfunction, skin
depigmentation, recurrence of the deformation of the eyelashes, scar progression and
rarely, retinal tear and detachment, visual loss, lid notching, acceleration of symblepharon
formation, xerosis, cellulitis, conjunctival hyperaemia, conjunctival chemosis, macular
drag, macula pucker, retinal folds, conjunctival lacerations, vitreous haemorrhages/retinal
haemorrhages, increase in IOP caused by gas injection during pneumatic retinopexy,
damage to surrounding tissue area, dispersion of RPE cells after cryopexy, diplopia, and
cryo-induced chorioretinal adhesion.
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In the event of failure to defrost the user may be unable to remove the probe tip from the
eye
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Only the areas of the eye to be treated should make contact with the probe tip or probe
shaft
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Do not fit mains power adapter into a damaged mains outlet socket.
•
Route power cords safely to eliminate risk of tripping or damage to user.
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High pressure gases are present inside the unit. Maximum operating pressure 45
Bar / 650 PSI, maximum cylinder pressure 83 Bar / 1200 PS.
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Observe the usual safety precautions associated with the use of medical gases, at all times.
Copies of these guidelines will be available from the gas supplier.
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Ensure the correct disposition of gas exhausted from the system so as to minimise the
exposure to Nitrous Oxide or Carbon Dioxide. This is the responsibility of the user.
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Ensure that sufficient gas is available in the cylinder prior to operation. TEST
BEFORE USE. If in doubt ensure that a replacement cylinder is immediately
available at the point of use.
CAUTION
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Use only genuine Keeler approved parts and accessories or device safety and performance
may be compromised.
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Keep out of the reach of children.
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To prevent condensation from forming, allow instrument to come to room temperature
before use.
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For indoor use only, in a sterile hospital environment.
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There are no user serviceable parts inside. Contact authorised service representative for
further information.
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