FDA Adverse Event
Injury
Summary report: N
SUNMED
MDR report key: 4469144
·
Received January 5, 2015
Report
- Report Number
- 2183650-2014-00006
- Event Type
- Injury
- Date Received
- January 5, 2015
- Manufacturer
- SUNMED INC.
- Product Code
- BSR
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
MERCURY MEDICAL DISTRIBUTED DEVICE COMPLAINT. COMPLAINT #(B)(4). PATIENT REMAINS HOSPITALIZED WITH NOTED DAILY IMPROVEMENT AND FUTURE DISCHARGE PLANNING.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 4890 | SUNMED | ENDOTRACHEAL TUBE INTRODUCER | BSR | SUNMED INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |