URINARY CATHETER 02016559

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,08 report with the FDA on 2015-03-26 for URINARY CATHETER 02016559 manufactured by Unomedical S.r.o..

Event Text Entries

[5617535] It was reported that upon receipt, the urinary catheter appeared to have been "folded". No pt involvement was reported.
Patient Sequence No: 1, Text Type: D, B5


[13097064] Based on the available info, this event is deemed a reportable malfunction. There were no reports of the pt being harmed as a result of this malfunction. Additional pt/event details have been requested. Should additional info become available, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3005778470-2015-00005
MDR Report Key4641722
Report Source01,08
Date Received2015-03-26
Date of Report2015-02-20
Date Mfgr Received2015-02-20
Date Added to Maude2015-05-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMATTHEW WALENCIAK, INTE ASSO DIR
Manufacturer Street211 AMERICAN AVE.
Manufacturer CityGREENSBORO NC 27409
Manufacturer CountryUS
Manufacturer Postal27409
Manufacturer Phone9083779293
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameURINARY CATHETER
Generic NameCONNECTOR, CATHETER
Product CodeGCD
Date Received2015-03-26
Model Number02016559
Lot Number169016
OperatorOTHER
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerUNOMEDICAL S.R.O.
Manufacturer AddressPRIEMYSELNY PARK 3 MICHALOVCE 07101 LO 07101


Patients

Patient NumberTreatmentOutcomeDate
10 2015-03-26

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