FDA Adverse Event
No answer provided
Summary report: N
COR25000315-000
MDR report key: 22699129
·
Received August 1, 2025
Report
- Report Number
- COR25000315-000
- Event Type
- No answer provided
- Date Received
- August 1, 2025
- Report Date
- August 1, 2025
- Product Code
- IZL
- Report Source
- Manufacturer report
- Reporter Location
- BE
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 333982 | IZL |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |