FDA Adverse Event Other Summary report: N

*

MDR report key: 901843 · Received March 27, 2007

Report

Report Number
9611112-2007-00001
Event Type
Other
Date Received
March 27, 2007
Manufacturer
HEBUMEDICAL GMBH
Product Code
HXD
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * HXD HEBUMEDICAL GMBH * *

Patients

Seq Age Sex Outcome Treatment
1