FEMOSOFT URETHRAL INSERT FEMSOFT INSERT 71201

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 02,05 report with the FDA on 2003-04-11 for FEMOSOFT URETHRAL INSERT FEMSOFT INSERT 71201 manufactured by Rochester Medical Corporation.

Event Text Entries

[331906] Patient reported episode of buring/pain with urination. Patient self medicated with antibiotic for 5 days. Patient reported episode to clinical coordinator at next scheduled follow-up visit.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2130787-2003-00005
MDR Report Key455032
Report Source02,05
Date Received2003-04-11
Date of Report2003-04-11
Date of Event2003-02-14
Date Mfgr Received2003-03-26
Date Added to Maude2003-04-23
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 ContactROBERT ANGLIN
Manufacturer StreetONE ROCHESTER MEDICAL DRIVE
Manufacturer CitySTEWARTVILLE MN 55976
Manufacturer CountryUS
Manufacturer Postal55976
Manufacturer Phone*
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFEMOSOFT URETHRAL INSERT
Generic NameTRANSURETHRAL OCCLUSION DEVICE
Product CodeMNG
Date Received2003-04-11
Model NumberFEMSOFT INSERT
Catalog Number71201
Lot Number*
ID Number*
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key444029
ManufacturerROCHESTER MEDICAL CORPORATION
Manufacturer AddressONE ROCHESTER MEDICAL DRIVE STEWARTVILLE MN 55976 US
Baseline Brand NameFEMSOFT URETRAL INSERT
Baseline Generic NameFEMALE TRANSURETHRAL OCCLUSION DEVICE
Baseline Model NoFEMSOFT INSERT
Baseline Catalog No72202
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2003-04-11

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