WHISTLE TIP URETERAL CATHETER 331104

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 2000-10-30 for WHISTLE TIP URETERAL CATHETER 331104 manufactured by Rusch Mfg (uk) Ltd..

Event Text Entries

[168982] It was reported that the catheter broke off inside the pt during ureteral stent placement. It was retrieved and another catheter was re-inserted without further incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010095-2000-00094
MDR Report Key302815
Report Source05,06
Date Received2000-10-30
Date of Report2000-10-30
Date Mfgr Received2000-10-16
Date Added to Maude2000-11-03
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 ContactKATRINA HALBIG, ADMINISTRATOR
Manufacturer Street2450 MEADOWBROOK PKWY
Manufacturer CityDULUTH GA 30136
Manufacturer CountryUS
Manufacturer Postal30136
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 URETERAL CATHETER
Generic NameURETERAL CATHETER
Product CodeFGF
Date Received2000-10-30
Returned To Mfg2000-10-16
Model NumberNA
Catalog Number331104
Lot NumberG990108
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key293096
ManufacturerRUSCH MFG (UK) LTD.
Manufacturer AddressHALIFAX RD. CRESSEX INDUSTRIAL ESTATE HIGH WYCOMBE, BUCKINGHAMSHIRE UK
Baseline Brand NameWHITLE TIP URETERAL CATHETER
Baseline Generic NameURETERAL CATHETER
Baseline Model NoNA
Baseline Catalog No331104
Baseline IDNA
Baseline Device FamilyURETHERAL CATHETER
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]59
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2000-10-30

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.