FDA Adverse Event
No answer provided
Summary report: N
COR25000058-000
MDR report key: 21303392
·
Received February 3, 2025
Report
- Report Number
- COR25000058-000
- Event Type
- No answer provided
- Date Received
- February 3, 2025
- Report Date
- February 3, 2025
- Product Code
- MKB
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1245935 | MKB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |