FDA Adverse Event Injury Summary report: N

2916714-2006-00078

MDR report key: 791142 · Received November 17, 2006

Report

Report Number
2916714-2006-00078
Event Type
Injury
Date Received
November 17, 2006
Product Code
HWC
Report Source
Manufacturer report

Narratives

Additional Manufacturer Narrative · 1

PRODUCT IS NOT AVAILABLE FOR EVALUATION. ALL AVAILABLE INFO HAS BEEN FORWARDED FOR ANALYSIS TO THE MFR, INION OY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HWC

Patients

Seq Age Sex Outcome Treatment
1