FDA Adverse Event Death Summary report: N

COLUMBIA KENDALL MED CTR COMP MEMBRANE PACK

MDR report key: 294042 · Received August 29, 2000

Report

Report Number
2184009-2000-00069
Event Type
Death
Date Received
August 29, 2000
Date of Event
July 21, 2000
Report Date
August 22, 2000
Manufacturer
MEDTRONIC PERFUSION SYSTEMS
Product Code
DWF
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COLUMBIA KENDALL MED CTR COMP MEMBRANE PACK CUSTOM TUBING PACK DWF MEDTRONIC PERFUSION SYSTEMS OK31R2 0004002065

Patients

Seq Age Sex Outcome Treatment
1