FDA Adverse Event
Injury
Summary report: N
COMPONENT CENTRAL MONITOR
MDR report key: 393458
·
Received May 10, 2002
Report
- Report Number
- 1218950-2002-00068
- Event Type
- Injury
- Date Received
- May 10, 2002
- Date of Event
- April 11, 2002
- Report Date
- April 12, 2002
- Manufacturer
- AGILENT TECHNOLOGIES, INC
- Product Code
- MHX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FI
- Reporter Occupation
- BIOMEDICAL ENGINEER
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE CENTRAL STATION DID NOT ALARM FOR VENTRICULAR TACHYCARDIA.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | COMPONENT CENTRAL MONITOR | CCM | MHX | AGILENT TECHNOLOGIES, INC | M2360A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Life Threatening |