FDA Adverse Event
No answer provided
Summary report: N
COR19000150-000
MDR report key: 8432122
·
Received March 18, 2019
Report
- Report Number
- COR19000150-000
- Event Type
- No answer provided
- Date Received
- March 18, 2019
- Report Date
- March 11, 2019
- Product Code
- RCE
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 220581 | RCE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |