Alcon monarch iii injector

Well where to. The agent also assumes it is still be automatically. Go back to all articles.

In addition, patients should be warned that they will need to exercise caution when engaging in activities that require good vision in dimly lit environments, such as driving at night or in poor visibility conditions, especially in the presence of oncoming traffic.

It is possible to experience very bothersome visual disturbances, significant enough that the patient could request explant of the IOL. Prior to surgery, physicians should provide prospective patients with a copy of the Patient Information Brochure available from Alcon informing them of possible risks and benefits associated with these IOLs.

Evaluation of clarity characteristics in a new hydrophobic acrylic IOL. J Cataract Refract Surg. Lehmann, R. Clin Ophthalmol. Published Apr Lee B. Comparison of the rotational stability of two toric intraocular lenses in consecutive eyes. Read all instructions prior to use. The handpiece is non-sterile and must be cleaned and sterilized prior to each use refer to Handpiece Preparation section of this Instructions for Use.

Failure to properly sterilize handpiece could result in serious infection e. Use of hydrogen peroxide may discolor titanium instruments. Study Description. Detailed Description:. FDA Resources. Arms and Interventions. Motorised injection device for intraocular lens implantation. Manual, plunger type injection device for intraocular lens implantation. Manual, screw type injection device for intraocular lens implantation.

Outcome Measures. Secondary Outcome Measures : Trypan Blue ingress into the anterior chamber in log units [ Time Frame: 1 minute after surgery ] Incision morphology - qualitative [ Time Frame: 1 day, 1 week and 1 month after surgery ]. Eligibility Criteria. Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Inclusion Criteria: Patients undergoing phacoemulsification for age-related uncomplicated cataracts through a 2.

Contacts and Locations. Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials. More Information. Layout table for additonal information Responsible Party: Abhay R. Vasavada, M. Intraocular lens implantation.

National Library of Medicine U. National Institutes of Health U. Department of Health and Human Services. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators.

Not Applicable. Study Type :. Interventional Clinical Trial. Actual Enrollment :. Study Start Date :.

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