FDA Adverse Event
Other
Summary report: N
AXIOS D
MDR report key: 536840
·
Received March 17, 2004
Report
- Report Number
- 1028232-2004-00040
- Event Type
- Other
- Date Received
- March 17, 2004
- Report Date
- March 11, 2004
- Manufacturer
- BIOTRONIK GMBH & CO.
- Product Code
- DXY
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
PACEMAKER COULD NOT BE INTERROGATED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | AXIOS D | PACEMAKER | DXY | BIOTRONIK GMBH & CO. | 338 843 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Hospitalization |