FDA Adverse Event
Injury
Summary report: N
NIMBUS 4
MDR report key: 3233285
·
Received July 11, 2013
Report
- Report Number
- 3005619970-2013-00008
- Event Type
- Injury
- Date Received
- July 11, 2013
- Manufacturer
- GETINGE SUZHOU CO. LTD.
- Product Code
- FNM
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THIS REPORT IS BEING FILED UNDER (B)(4) BY ARJOHUNTLEIGH, INC. ON BEHALF OF THE MANUFACTURER (GETINGE (B)(4)). ADDITIONAL INFO WILL BE PROVIDED UPON CONCLUSION OF THE MANUFACTURER'S INVESTIGATION.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 320013 | NIMBUS 4 | FNM | GETINGE SUZHOU CO. LTD. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |