FDA Adverse Event Malfunction Summary report: N

*

MDR report key: 1182524 · Received July 21, 2008

Report

Report Number
8010042-2008-00107
Event Type
Malfunction
Date Received
July 21, 2008
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
CBK
PMA / PMN Number
k063404
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1