MAUDE MDR 522572
- MDR report key
- 522572
- Report number
- 1018233-2004-00017
- Event key
- 0
- Event type
- 3
- Date of event
- 2004-01-22
- Date received
- 2004-04-22
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 500
- Health professional
- 3
- Initial report to FDA
- 3
- Event location
- 3
Devices#
Seq, Brand, Generic table| Seq | Brand | Generic | Manufacturer | Product code | Model | Catalog | Lot | PMA | 510(k) | Implant | Evaluated | Availability |
|---|
| 1 | * | WOUND DRAIN | C.R. BARD, INC. | GCY | NA | UNK | UNK | | | N | R | |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2004-04-22 | 0 |
|
Event Narratives#
No narrative records found.