FDA Adverse Event
Summary report: N
SWAN-GANZ, 7.5 FR
MDR report key: 30039
·
Received January 16, 1996
Report
- Report Number
- 30039
- Date Received
- January 16, 1996
- Report Date
- January 16, 1996
- Manufacturer
- AMERICAN EDWARDS LABORATORIES
- Product Code
- DYG
- Report Source
- User Facility report
Narratives
Description of Event or Problem · 1
VIP+CATHETER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SWAN-GANZ, 7.5 FR | SWAN-GANZ, 7.5 FR | DYG | AMERICAN EDWARDS LABORATORIES |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |