MAUDE MDR 9884162
- MDR report key
- 9884162
- Report number
- 3006260740-2020-01066
- Event key
- 0
- Event type
- 3
- Date received
- 2020-03-26
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 100
- 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 | POWERPICC PROVENA 5F TRIPLE LUMEN | CATHETER,INTRAVASCULAR,THERAPEUTIC,LONG-TERM GREATER THAN 30 DAYS | BARD ACCESS SYSTEMS | LJS | N/A | UNKNOWN | UNK | | | | N
| R |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2020-03-26 | 0 |
|
Event Narratives#
No narrative records found.