FDA Adverse Event Injury Summary report: N

L-ANEURYSM-CLIP APPLIER

MDR report key: 2849320 · Received November 9, 2012

Report

Report Number
8010890-2012-00001
Event Type
Injury
Date Received
November 9, 2012
Date of Event
June 26, 2012
Report Date
October 29, 2012
Manufacturer
PETER LAZIC GMBH
Product Code
HCH
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 L-ANEURYSM-CLIP APPLIER ANEURYSM CLIP APPLIER HCH PETER LAZIC GMBH 45.441 J137717

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| L