FDA Adverse Event Injury Summary report: N

PHILOS II DR

MDR report key: 1211775 · Received October 24, 2008

Report

Report Number
1028232-2008-01280
Event Type
Injury
Date Received
October 24, 2008
Date of Event
September 15, 2008
Report Date
September 24, 2008
Manufacturer
BIOTRONIK GMBH AND CO.
Product Code
DXY
PMA / PMN Number
P950037
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

THIS SYSTEM WAS REMOVED DUE TO INFECTION. PHILOS II DR, MDR 1028232-2008-01280. SETROX S 45, MDR 1028232-2008-01281.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PHILOS II DR PACEMAKER DXY BIOTRONIK GMBH AND CO. 341826

Patients

Seq Age Sex Outcome Treatment
1 79 YR Hospitalization