BELLUCCI SCISSORS N1705 QS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1997-04-11 for BELLUCCI SCISSORS N1705 QS manufactured by Storz Instrument Co..

Event Text Entries

[18949543] During a tympanoplasty (ear drum repair) procedure, a blade from this pair of scissors broke off. The blade was retrieved and the procedure was completed without problems.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1932180-1997-00039
MDR Report Key83126
Report Source05
Date Received1997-04-11
Date of Report1997-03-12
Date Facility Aware1996-12-26
Report Date1997-03-12
Date Reported to Mfgr1997-03-12
Date Mfgr Received1997-03-12
Date Added to Maude1997-04-15
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 NameBELLUCCI SCISSORS
Generic NameEAR SCISSORS
Product CodeJZB
Date Received1997-04-11
Model NumberNA
Catalog NumberN1705 QS
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age3 YR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key82474
ManufacturerSTORZ INSTRUMENT CO.
Manufacturer Address499 SOVEREIGN CT. ST. LOUIS MO 63011 US
Baseline Brand NameBELUCCI SCISSORS
Baseline Generic NameEAR SCISSORS
Baseline Model NoNA
Baseline Catalog NoN1705 QS
Baseline IDNA
Baseline Device FamilyEAR SCISSORS
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 1997-04-11

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