FDA Adverse Event
Other
Summary report: N
PRECISE DESK TOP 4.1
MDR report key: 526281
·
Received May 24, 2004
Report
- Report Number
- 9617016-2004-00010
- Event Type
- Other
- Date Received
- May 24, 2004
- Date of Event
- April 15, 2004
- Report Date
- May 24, 2004
- Manufacturer
- ELEKTA LIMITED
- Product Code
- IYE
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MD, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
THE CUSTOMER HAS REQUESTED INHIBIT OF OUT-OF-ROOM ASSISTED SET-UP (ASU) UNDER SPECIFIC CONDITIONS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PRECISE DESK TOP 4.1 | MEDICAL LINEAR ACCELERATOR CONTROL SYSTEM | IYE | ELEKTA LIMITED | MRT 7781 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Other |