MAUDE MDR 471099
- MDR report key
- 471099
- Report number
- 1018233-2003-00029
- Event key
- 0
- Event type
- 3
- Date of event
- 2003-05-18
- Date received
- 2003-07-09
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 0
- Health professional
- 3
- Initial report to FDA
- 3
- Event location
- 0
Devices#
Seq, Brand, Generic table| Seq | Brand | Generic | Manufacturer | Product code | Model | Catalog | Lot | PMA | 510(k) | Implant | Evaluated | Availability |
|---|
| 1 | * | * | C.R. BARD, INC. | GCY | NA | * | UNK | | | N | R | * |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2003-07-09 | 0 |
|
Event Narratives#
No narrative records found.