FDA Adverse Event Death Summary report: N

SERVO-I

MDR report key: 1052223 · Received May 22, 2008

Report

Report Number
1225700-2008-00072
Event Type
Death
Date Received
May 22, 2008
Date of Event
April 19, 2008
Report Date
May 8, 2008
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
CBK
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
NJ, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SERVO-I CBK CBK MAQUET CRITICAL CARE AB * *

Patients

Seq Age Sex Outcome Treatment
1 * Death