FDA Adverse Event Other Summary report: N

AIRWAY BASIC TRACHEAL

MDR report key: 479777 · Received August 20, 2003

Report

Report Number
9681384-2003-00013
Event Type
Other
Date Received
August 20, 2003
Date of Event
November 1, 2002
Report Date
August 19, 2003
Manufacturer
MMJ S.A. DE C.V. PLANT 2
Product Code
CBH
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AIRWAY BASIC TRACHEAL TRACHEAL TUBE WITH LANZ PRESSURE REGULAT CBH MMJ S.A. DE C.V. PLANT 2 NA UNK

Patients

Seq Age Sex Outcome Treatment
1