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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NIDEK LASIK MACHINE NONE

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NIDEK LASIK MACHINE NONE Back to Search Results
Event Date 05/25/2006
Event Type  Injury  
Event Description

Following lasik surgery, i have continued to be plagued by very severe dry eye syndrome to the point of disability. Severe associated pain, with occasional mild loss of vision or diplopia.

 
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Brand NameNIDEK LASIK MACHINE
Type of DeviceNONE
MDR Report Key1513544
Report NumberMW5013097
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 10/16/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/16/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Is The Reporter A Health Professional? Yes

Patient TREATMENT DATA
Date Received: 10/16/2009 Patient Sequence Number: 1
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