FDA Adverse Event
Injury
Summary report: N
*
MDR report key: 1258575
·
Received November 24, 2008
Report
- Report Number
- 2243969-2008-00012
- Event Type
- Injury
- Date Received
- November 24, 2008
- Manufacturer
- CONVATEC, A DIVISION OF E.R. SQUIBB & SONS, L.L.C.
- Product Code
- KNT
- PMA / PMN Number
- k032734
- Report Source
- Manufacturer report
- Reporter Occupation
- INVALID DATA
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | * | KNT | CONVATEC, A DIVISION OF E.R. SQUIBB & SONS, L.L.C. | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |