MAUDE MDR 9774999
- MDR report key
- 9774999
- Report number
- 3005099803-2020-00560
- Event key
- 0
- Event type
- 3
- Date of event
- 2019-12-11
- Date received
- 2020-03-02
- Adverse event
- 3
- Product problem
- 3
- Patients in event
- 0
- Reporter occupation
- 1
- 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 | CRE FIXED WIRE | DILATOR, ESOPHAGEAL | BOSTON SCIENTIFIC CORPORATION | KNQ | M00558330 | 5833 | 0023518785 | | | | Y
| R |
Patients#
Sequence, Received, Treatment table| Sequence | Received | Treatment | Outcome |
|---|
| 1 | 2020-03-02 | 0 |
|
Event Narratives#
No narrative records found.