FDA Adverse Event Death Summary report: N

9681384-2000-00003

MDR report key: 277481 · Received May 10, 2000

Report

Report Number
9681384-2000-00003
Event Type
Death
Date Received
May 10, 2000
Date of Event
February 26, 2000
Manufacturer
MMJ SA DE CV
Product Code
BTR
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BTR MMJ SA DE CV

Patients

Seq Age Sex Outcome Treatment
1