FDA Adverse Event
Other
Summary report: N
COR18001652-000
MDR report key: 7984919
·
Received October 18, 2018
Report
- Report Number
- COR18001652-000
- Event Type
- Other
- Date Received
- October 18, 2018
- Report Date
- October 18, 2018
- Manufacturer
- Lumenis, Inc.
- Product Code
- GEX
- Report Source
- Manufacturer report
- Reporter Location
- UT, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 817191 | GEX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |