FDA Adverse Event Malfunction Summary report: N

HAMILTON MEDICAL, INC.

MDR report key: 354710 · Received October 5, 2001

Report

Report Number
2937708-2001-00003
Event Type
Malfunction
Date Received
October 5, 2001
Date of Event
August 29, 2001
Manufacturer
HAMILTON MEDICAL, INC.
Product Code
CBK
Report Source
Manufacturer report
Reporter Location
NV, US
Reporter Occupation
RISK MANAGER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
44882 HAMILTON MEDICAL, INC. TRANSPORT VENTILATOR CBK HAMILTON MEDICAL, INC. * *

Patients

Seq Age Sex Outcome Treatment
1