FDA Adverse Event
Death
Summary report: N
MEDRAD ANGIOGRAPHIC INJECTOR
MDR report key: 111800
·
Received August 6, 1997
Report
- Report Number
- 2520313-1997-00031
- Event Type
- Death
- Date Received
- August 6, 1997
- Manufacturer
- MEDRAD, INC.
- Product Code
- DXT
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MEDRAD ANGIOGRAPHIC INJECTOR | ANGIOGRAPHIC INJECTOR | DXT | MEDRAD, INC. | MKIV | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |