MAUDE MDR 8745173
- MDR report key
- 8745173
- Report number
- 1950204-2019-00220
- Event key
- 0
- Event type
- 3
- Date received
- 2019-06-28
- 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 GRAM NEGATIVE IDENTIFICATION TEST KIT | VITEK? 2 GN ID TEST KIT | BIOMERIEUX INC. | LQM | | 21341 | 2410734103 | | | | R
| N |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2019-06-28 | 0 |
|
Event Narratives#
No narrative records found.