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ECLIPSE Adverse Event — Malfunction (MDR 3003793371-2008-00002)

ECLIPSE Adverse Event — Malfunction (MDR 3003793371-2008-00002) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ECLIPSE; Generic name: TREATMENT PLANNING; Manufacturer: VARIAN MEDICAL SYSTEMS.

DeviceECLIPSE
Generic nameTREATMENT PLANNING
ManufacturerVARIAN MEDICAL SYSTEMS
Report number3003793371-2008-00002
Event typeMalfunction
Product problemY
Date received2008-02-14
Report sourceHealth Professional, User facility, HEALTH PROFESSIONAL, USE
SourceopenFDA MAUDE (device adverse events)

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