FDA Adverse Event Injury Summary report: N

TECNOL MEDICAL PRODUCTS, INC

MDR report key: 61940 · Received January 8, 1997

Report

Report Number
1625443-1997-00001
Event Type
Injury
Date Received
January 8, 1997
Date of Event
November 8, 1996
Report Date
January 8, 1997
Product Code
BTX
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TECNOL MEDICAL PRODUCTS, INC ADULT ARTERIAL HAND-AID WRIST SUPPORT BTX NA UNK

Patients

Seq Age Sex Outcome Treatment
1 *