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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ALLEGRATTO WAVE LASIC

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ALLEGRATTO WAVE LASIC Back to Search Results
Event Date 09/11/2008
Event Type  Injury  
Event Description

There is epithelial ingrowth in both eyes and i can not see clearly near or distant both. Refraction test shows cylindrical, as well as spherical number in both eyes. All my jobs are suspended since the operation i. E. For the last 2 mos. Overall, the irregularities in the corneal surface is suspected to be responsible for all the existing problems.

 
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Type of DeviceALLEGRATTO WAVE LASIC
MDR Report Key1232234
Report NumberMW5008991
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation BIOMEDICAL ENGINEER
Type of Report Initial
Report Date 11/13/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received11/13/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 11/13/2008 Patient Sequence Number: 1
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