FDA Adverse Event Injury Summary report: N

2925153-2000-00017

MDR report key: 320453 · Received March 12, 2001

Report

Report Number
2925153-2000-00017
Event Type
Injury
Date Received
March 12, 2001
Date of Event
November 9, 2000
Product Code
---
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
11009 ---

Patients

Seq Age Sex Outcome Treatment
1