FDA Adverse Event
No answer provided
Summary report: N
COR18001126-000
MDR report key: 7621238
·
Received June 20, 2018
Report
- Report Number
- COR18001126-000
- Event Type
- No answer provided
- Date Received
- June 20, 2018
- Report Date
- June 20, 2018
- Product Code
- PDZ
- 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 |
|---|---|---|---|---|---|---|---|
| 460126 | PDZ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |