FDA Adverse Event
Summary report: N
BVI9400
MDR report key: 1645772
·
Received March 11, 2010
Report
- Report Number
- 1645772
- Date Received
- March 11, 2010
- Date of Event
- January 12, 2010
- Report Date
- March 11, 2010
- Manufacturer
- VERATHON
- Product Code
- EXQ
- Report Source
- User Facility report
- Reporter Location
- MI, US
Narratives
Description of Event or Problem · 1
THE READINGS ON THE BLADDER SCANNER THE NURSE WAS USING WERE NOT CONSISTENT WITH THE READINGS FROM ANOTHER ONE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BVI9400 | BLADDER SCANNER | EXQ | VERATHON | BVI9400 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |