WHISTLE TIP 331103

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 2003-10-07 for WHISTLE TIP 331103 manufactured by Rusch, Inc..

Event Text Entries

[20690573] Describe event or problem: tip broke.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2429473-2003-00221
MDR Report Key489218
Report Source05
Date Received2003-10-07
Date of Report2003-10-06
Date Mfgr Received2003-10-02
Date Added to Maude2003-10-17
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
Manufacturer ContactROLANDA SCOTT COORD.
Manufacturer Street2450 MEADOWBROOK PARKWAY
Manufacturer CityDULUTH GA 30096
Manufacturer CountryUS
Manufacturer Postal30096
Manufacturer Phone7706230816
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameWHISTLE TIP
Generic NameUROLOGICAL
Product CodeFGF
Date Received2003-10-07
Model NumberNA
Catalog Number331103
Lot Number121055
ID NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key477996
ManufacturerRUSCH, INC.
Manufacturer Address2450 MEADOWBROOK PKWY. DULUTH GA 30096 US
Baseline Brand NameWHISTLE TIP URETERAL CATHETER
Baseline Generic NameURETERAL CATHETERS
Baseline Model NoNA
Baseline Catalog No331103
Baseline IDNA
Baseline Device FamilyUROLOGICAL DEVICES
Baseline Shelf Life Contained*
Baseline Shelf Life [Months]*
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2003-10-07

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