FDA Adverse Event Injury Summary report: N

QUADROX-I ADULT

MDR report key: 14755658 · Received April 5, 2012

Report

Report Number
8010762-2012-00006
Event Type
Injury
Date Received
April 5, 2012
Date of Event
March 7, 2012
Report Date
March 7, 2012
Manufacturer
MAQUET CARDIOPULMONARY AG
Product Code
MAQ
PMA / PMN Number
K082117
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUADROX-I ADULT MAQ MAQUET CARDIOPULMONARY AG NA 70073652

Patients

Seq Age Sex Outcome Treatment
1 NI Unknown Disability