7.5V TRANSFORMER N1011

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 1996-11-12 for 7.5V TRANSFORMER N1011 manufactured by Storz Instrument Company.

Event Text Entries

[30390] This transformer does not have a ground wire. This problem was found upon incoming inspection.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1932180-1996-00105
MDR Report Key48692
Report Source06
Date Received1996-11-12
Date of Report1996-10-14
Date of Event1996-10-14
Date Facility Aware1996-10-14
Report Date1996-10-14
Date Reported to Mfgr1996-10-14
Date Mfgr Received1996-10-14
Date Added to Maude1996-11-15
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 Name7.5V TRANSFORMER
Generic NameTRANSFORMER
Product CodeHPQ
Date Received1996-11-12
Model NumberNA
Catalog NumberN1011
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age*
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key49456
ManufacturerSTORZ INSTRUMENT COMPANY
Manufacturer Address499 SOVEREIGN COURT ST LOUIS MO 63601 US
Baseline Brand NameSTORZ 7.5V TRANSFORMER
Baseline Generic NameTRANSFORMER
Baseline Model NoNA
Baseline Catalog NoN1011
Baseline IDNA
Baseline Device FamilyHEADLIGHT TRANSFORMER
Baseline Shelf Life ContainedN
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 1996-11-12

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