FDA Adverse Event Injury Summary report: N

NEONATAL & PEDIATRIC ENDOTRACHEAL TUBE HOLDER

MDR report key: 1013033 · Received February 29, 2008

Report

Report Number
1217052-2008-00032
Event Type
Injury
Date Received
February 29, 2008
Report Date
February 8, 2008
Manufacturer
SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.
Product Code
CBH
Adverse Event
Yes
Product Problem
Yes
Report Source
Distributor report
Reporter Location
SD, US
Reporter Occupation
PHYSICIAN

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NEONATAL & PEDIATRIC ENDOTRACHEAL TUBE HOLDER 73 BTR - ENDOTRACHEAL TUBE HOLDER CBH SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V. * *

Patients

Seq Age Sex Outcome Treatment
1 *