FDA Adverse Event
Injury
Summary report: N
2110898-1997-00021
MDR report key: 110267
·
Received July 29, 1997
Report
- Report Number
- 2110898-1997-00021
- Event Type
- Injury
- Date Received
- July 29, 1997
- Date of Event
- June 5, 1997
- Manufacturer
- 3M SARNS
- Product Code
- HRX
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HRX | 3M SARNS | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |