FDA Adverse Event Injury Summary report: N

HANS RUDOLPH, INC.

MDR report key: 504914 · Received December 31, 2003

Report

Report Number
MW1030680
Event Type
Injury
Date Received
December 31, 2003
Date of Event
December 29, 2003
Report Date
December 31, 2003
Manufacturer
*
Product Code
BYG
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
PATIENT

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HANS RUDOLPH, INC. FULL FACE/ORO-NASAL/C-PAP/NPP MASK BYG * 7600 SERIES *

Patients

Seq Age Sex Outcome Treatment
1 65 YR