STARTER KIT, SIZE 4, 1214

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,07 report with the FDA on 1997-11-12 for STARTER KIT, SIZE 4, 1214 manufactured by Uromed Corp..

Event Text Entries

[75120] Pt reported a strong urge to void, when voiding she forgot to remove the device. Pt assumed device had fallen into toilet but could not confirm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1224675-1997-00051
MDR Report Key132447
Report Source04,07
Date Received1997-11-12
Date of Report1997-10-21
Date of Event1997-10-15
Date Mfgr Received1997-10-17
Device Manufacturer Date1996-10-01
Date Added to Maude1997-11-18
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 Location0
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTARTER KIT, SIZE 4, 1214
Generic NameRELIANCE
Product CodeMNG
Date Received1997-11-12
Model NumberSIZE 4
Catalog Number1214
Lot Number0000000009
ID Number*
Device Expiration Date1998-10-01
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key129464
ManufacturerUROMED CORP.
Manufacturer Address64 A ST. NEEDHAM MA 02194 US
Baseline Brand NameRELIANCE
Baseline Generic NameURETHRAL OCCLUSION DEVICE
Baseline Model NoSIZE 4
Baseline Catalog No1204
Baseline ID*
Baseline Device FamilyURINARY CONTROL INSERT
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]24
Baseline PMA FlagY
Premarket ApprovalP9600
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1997-11-12

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