FDA Adverse Event
Injury
Summary report: N
8030904-2005-00001
MDR report key: 635333
·
Received August 26, 2005
Report
- Report Number
- 8030904-2005-00001
- Event Type
- Injury
- Date Received
- August 26, 2005
- Date of Event
- May 23, 2005
- Manufacturer
- RADI MEDICAL SYSTEMS AB
- Product Code
- DQX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DQX | RADI MEDICAL SYSTEMS AB | 12005 | 051193 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |