FDA Adverse Event Malfunction Summary report: N

SKATER INTRODUCER SYSTEM

MDR report key: 5145138 · Received September 20, 2004

Report

Report Number
1036710-2004-00006
Event Type
Malfunction
Date Received
September 20, 2004
Manufacturer
MEDICAL DEVICE TECHNOLOGIES, INC.
Product Code
DYB
Report Source
Manufacturer report

Narratives

Description of Event or Problem · 1

MISUSE OF THE PRODUCT BY THE ATTENDING PHYSICIAN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SKATER INTRODUCER SYSTEM DRAINAGE CATHETER ACCESSORY DYB MEDICAL DEVICE TECHNOLOGIES, INC. 40990S0O

Patients

Seq Age Sex Outcome Treatment
1