CONVEEN OPTIMA ?30 2203001004

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign report with the FDA on 2016-01-22 for CONVEEN OPTIMA ?30 2203001004 manufactured by Coloplast A/s.

Event Text Entries

[36687767] Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence, should additional facts prompt us to alter or supplement any information of conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[36687768] The urisheath was very difficult to remove with warm water, this has caused skin abrasion. The skin has been healed completely since then as he has used barrier cream to treat the lesion and he discontinued with urisheaths for some days. He has used incontinence pads instead. Consumer is wearing the urisheaths for some hours only (less than 24 hours) so he should use adhesive remover to remove the urisheath in case he has difficulties to remove it with water.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006606901-2016-00001
MDR Report Key5386627
Report SourceCONSUMER,FOREIGN
Date Received2016-01-22
Date of Report2016-01-22
Date Mfgr Received2015-12-29
Date Added to Maude2016-01-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactCHRISTINE BUCKVOLD
Manufacturer Street1601 WEST RIVER ROAD NORTH
Manufacturer CityMINNEAPOLIS MN 55411
Manufacturer CountryUS
Manufacturer Postal55411
Manufacturer Phone6123024982
Manufacturer G1COLOPLAST A/S NYIRBATOR
Manufacturer StreetCOLOPLAST UTCA 2
Manufacturer CityNYIRBATOR, 4300
Manufacturer CountryHU
Manufacturer Postal Code4300
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONVEEN OPTIMA ?30
Generic NameMALE EXTERNAL CATHETER
Product CodeEXJ
Date Received2016-01-22
Model Number2203001004
Catalog Number2203001004
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOLOPLAST A/S
Manufacturer AddressHOLTEDAM 1 HUMLEBAEK, DA 3050 DA 3050


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-01-22

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