FDA Adverse Event
Injury
Summary report: N
1063481-2011-00055
MDR report key: 2209491
·
Received August 12, 2011
Report
- Report Number
- 1063481-2011-00055
- Event Type
- Injury
- Date Received
- August 12, 2011
- Report Date
- December 1, 2010
- Manufacturer
- ARTIVION, INC.
- PMA / PMN Number
- P010003
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TU
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |