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.
[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
Report Number | 2130787-2003-00005 |
MDR Report Key | 455032 |
Report Source | 02,05 |
Date Received | 2003-04-11 |
Date of Report | 2003-04-11 |
Date of Event | 2003-02-14 |
Date Mfgr Received | 2003-03-26 |
Date Added to Maude | 2003-04-23 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | ROBERT ANGLIN |
Manufacturer Street | ONE ROCHESTER MEDICAL DRIVE |
Manufacturer City | STEWARTVILLE MN 55976 |
Manufacturer Country | US |
Manufacturer Postal | 55976 |
Manufacturer Phone | * |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FEMOSOFT URETHRAL INSERT |
Generic Name | TRANSURETHRAL OCCLUSION DEVICE |
Product Code | MNG |
Date Received | 2003-04-11 |
Model Number | FEMSOFT INSERT |
Catalog Number | 71201 |
Lot Number | * |
ID Number | * |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 444029 |
Manufacturer | ROCHESTER MEDICAL CORPORATION |
Manufacturer Address | ONE ROCHESTER MEDICAL DRIVE STEWARTVILLE MN 55976 US |
Baseline Brand Name | FEMSOFT URETRAL INSERT |
Baseline Generic Name | FEMALE TRANSURETHRAL OCCLUSION DEVICE |
Baseline Model No | FEMSOFT INSERT |
Baseline Catalog No | 72202 |
Baseline ID | * |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2003-04-11 |