FDA Adverse Event
Malfunction
Summary report: N
1121308-2005-00035
MDR report key: 768702
·
Received December 9, 2005
Report
- Report Number
- 1121308-2005-00035
- Event Type
- Malfunction
- Date Received
- December 9, 2005
- Product Code
- HTW
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFO.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HTW |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |