FDA Adverse Event
Death
Summary report: N
VIRIDIA 26/24 COMPONENT MONITORING SYSTEM
MDR report key: 645231
·
Received November 8, 2005
Report
- Report Number
- 1218950-2005-00351
- Event Type
- Death
- Date Received
- November 8, 2005
- Date of Event
- October 28, 2005
- Report Date
- October 28, 2005
- Manufacturer
- AGILENT TECHNOLOGIES
- Product Code
- DRT
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- BIOMEDICAL ENGINEER
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE BEDSIDE MONITOR DID NOT ALARM WHEN THE PATIENT WENT INTO ASYSTOLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VIRIDIA 26/24 COMPONENT MONITORING SYSTEM | BEDSIDE MONITOR | DRT | AGILENT TECHNOLOGIES | M1205A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Death |