KAHN SCLERAL SHIELD ET4600

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1998-02-24 for KAHN SCLERAL SHIELD ET4600 manufactured by Storz Instrument Co..

Event Text Entries

[93300] The handle broke off of this scleral shield during a procedure. Another shield was used. There was no pt injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1932180-1998-00010
MDR Report Key151427
Report Source06
Date Received1998-02-24
Date of Report1998-01-27
Date of Event1998-01-22
Date Facility Aware1998-01-22
Report Date1998-01-27
Date Mfgr Received1998-01-22
Date Added to Maude1998-02-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKAHN SCLERAL SHIELD
Generic NameEYE SHIELD
Product CodeHOY
Date Received1998-02-24
Model NumberNA
Catalog NumberET4600
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeUNKNOWN
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key147571
ManufacturerSTORZ INSTRUMENT CO.
Manufacturer Address499 SOVEREIGN CT. MANCHESTER MO 63011 US
Baseline Brand NameKAHN SCLERAL SHIELD
Baseline Generic NameOPHTHALMIC EYE SHIELD
Baseline Model NoNA
Baseline Catalog NoET4600
Baseline IDNA
Baseline Device FamilyEYE SHIELD
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 1998-02-24

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