FDA Adverse Event Injury Summary report: N

*

MDR report key: 1258575 · Received November 24, 2008

Report

Report Number
2243969-2008-00012
Event Type
Injury
Date Received
November 24, 2008
Manufacturer
CONVATEC, A DIVISION OF E.R. SQUIBB & SONS, L.L.C.
Product Code
KNT
PMA / PMN Number
k032734
Report Source
Manufacturer report
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * KNT CONVATEC, A DIVISION OF E.R. SQUIBB & SONS, L.L.C. NA UNK

Patients

Seq Age Sex Outcome Treatment
1