MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2003-10-07 for WHISTLE TIP 331103 manufactured by Rusch, Inc..
[20690573]
Describe event or problem: tip broke.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2429473-2003-00221 |
MDR Report Key | 489218 |
Report Source | 05 |
Date Received | 2003-10-07 |
Date of Report | 2003-10-06 |
Date Mfgr Received | 2003-10-02 |
Date Added to Maude | 2003-10-17 |
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 | ROLANDA SCOTT COORD. |
Manufacturer Street | 2450 MEADOWBROOK PARKWAY |
Manufacturer City | DULUTH GA 30096 |
Manufacturer Country | US |
Manufacturer Postal | 30096 |
Manufacturer Phone | 7706230816 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | WHISTLE TIP |
Generic Name | UROLOGICAL |
Product Code | FGF |
Date Received | 2003-10-07 |
Model Number | NA |
Catalog Number | 331103 |
Lot Number | 121055 |
ID Number | N/A |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 477996 |
Manufacturer | RUSCH, INC. |
Manufacturer Address | 2450 MEADOWBROOK PKWY. DULUTH GA 30096 US |
Baseline Brand Name | WHISTLE TIP URETERAL CATHETER |
Baseline Generic Name | URETERAL CATHETERS |
Baseline Model No | NA |
Baseline Catalog No | 331103 |
Baseline ID | NA |
Baseline Device Family | UROLOGICAL DEVICES |
Baseline Shelf Life Contained | * |
Baseline Shelf Life [Months] | * |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | Y |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2003-10-07 |