MAUDE MDR 9853522
- MDR report key
- 9853522
- Report number
- 1950204-2020-00079
- Event key
- 0
- Event type
- 3
- Date received
- 2020-03-19
- 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 | VITEK? 2 AST-P652 TEST KIT | VITEK? 2 AST-P652 TEST KIT | BIOMERIEUX, INC. | LON | | 421857 | 8021232403 | | | | R
| N |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2020-03-19 | 0 |
|
Event Narratives#
No narrative records found.