FDA Adverse Event Death Summary report: N

SERVO-I

MDR report key: 1040168 · Received May 2, 2008

Report

Report Number
1225700-2008-00060
Event Type
Death
Date Received
May 2, 2008
Report Date
April 9, 2008
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
CBK
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
BR
Reporter Occupation
INVALID DATA

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