BLADE RING LEFT SIZE 5 N7519 L5

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 1998-04-29 for BLADE RING LEFT SIZE 5 N7519 L5 manufactured by Storz Instrument Company.

Event Text Entries

[17414475] This blade broke while being used on a pt. Another ring was used. There was no pt injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1932180-1998-00025
MDR Report Key165376
Report Source05,06
Date Received1998-04-29
Date of Report1998-04-02
Date of Event1998-03-30
Date Facility Aware1998-03-30
Report Date1998-04-02
Date Reported to Mfgr1998-04-02
Date Mfgr Received1998-04-02
Date Added to Maude1998-05-04
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 NameBLADE RING LEFT SIZE 5
Generic NameMOUTH GAG
Product CodeKBN
Date Received1998-04-29
Model NumberNA
Catalog NumberN7519 L5
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeUNKNOWN
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key160957
ManufacturerSTORZ INSTRUMENT COMPANY
Manufacturer Address499 SOVEREIGN CT. ST LOUIS MO 63011 US
Baseline Brand NameBLADE RING LEFT SIZE 5
Baseline Generic NameMOUTH GAG
Baseline Model NoNA
Baseline Catalog NoN7519 L5
Baseline IDNA
Baseline Device FamilyMOUTH GAG
Baseline Shelf Life ContainedA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 1998-04-29

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