FDA Adverse Event
Other
Summary report: N
COR21000123-000
MDR report key: 11723987
·
Received April 25, 2021
Report
- Report Number
- COR21000123-000
- Event Type
- Other
- Date Received
- April 25, 2021
- Report Date
- April 25, 2021
- Manufacturer
- Lumenis Ltd.
- Product Code
- GEX
- Report Source
- Manufacturer report
- Reporter Location
- IS
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 617948 | GEX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |